Contents and Contributor Listings for the Patai series
205
Contents and Contributor Listings for the Patai series
Transcript of Contents and Contributor Listings for the Patai series
Contents and Contributor Listings for the Patai series
The Chemistry of Alkenes, Volume 1 (1964) (See Volume 2 in 1970)
Edited by Saul Patai
Chapter 1. Wave mechanics and the alkene bondC. A. CoulsonMathematical Institute, University of Oxford, England
E. Theal StewartQueen’s College, Dundee, Scotland
Chapter 2. Elimination reactions in solutionWilliam H. Saunders Jr.University of Rochester, New York, U.S.A.
Chapter 3. Olefin-forming eliminations in the gas phaseAllan MaccollUniversity College, London, England
Chapter 4. Alkene-forming condensation reactionsThomas I. CrowellUniversity of Virginia, Charlottesville, Va., U.S.A.
Chapter 5. Detection and determination of the alkenesEdward J. KucharOlin Mathieson Chemical Corporation, New Haven, Conn., U.S.A.
Chapter 6. Alkene complexes of some transition metalsMichael CaisTechnion—Israel Institute of Technology, Haifa, Israel
Chapter 7. Alkene rearrangementsKenneth MackenzieBedford College, University of London, England
Chapter 8. Nucleophilic attacks on carbon–carbon double bondsSaul PataiThe Hebrew University, Jerusalem, Israel
Zvi RappoportThe Hebrew University, Jerusalem, Israel
Chapter 9. Reactions of alkenes with radicals and carbenesJohn I. G. CadoganSt. Salvator’s College, University of St. Andrews, Scotland
Michael J. PerkinsKing’s College, London, England
Chapter 10. Allylic reactionsRobert H. DeWolfeUniversity of California at Santa Barbara, U.S.A.
William G. YoungUniversity of California at Los Angeles, U.S.A.
1
Chapter 11. Cycloaddition reactions of alkenesRolf HuisgenUniversity of Munich, Germany
Rudolf GrasheyUniversity of Munich, Germany
Jurgen SauerUniversity of Munich, Germany
Chapter 12. Conjugated dienesMichael CaisTechnion—Israel Institute of Technology, Haifa, Israel
Chapter 13. CumulenesHerbert FischerMax Planck Institute, Heidelberg, Germany
Chapter 14. KetenesRichard N. LaceyB.P. Research Centre, Sunbury-on-Thames, England
The Chemistry of the Carbonyl Group, Volume 1, (1966) (See Volume 2 in 1970)
Edited by Saul Patai
Chapter 1. General and theoretical aspects of the carbonyl groupG. BerthierCentre National de la Recherche Scientifique, Paris, France
J. SerreEcole Normale Superieure, Paris, France
Chapter 2. Carbonyl-forming oxidationsC. F. CullisImperial College, London, England
A. FishImperial College, London, England
Chapter 3. Formation of carbonyl groups in hydrolytic reactionsPentti SalomaaUniversity of Turku, Finland
Chapter 4. Formation of aldehydes and ketones from carboxylic acids and their derivativesReynold. C. FusonUniversity of Nevada, U.S.A.
Chapter 5. Formation of ketones and aldehydes by acylation, formylation and some relatedprocessesD. P. N. SatchellKing’s College, London, England
R. S. SatchellQueen Elizabeth College, London, England
2
Chapter 6. Carbonyl syntheses through organometallicsMichael CaisTechnion—Israel Institute of Technology, Haifa, Israel
Asher MandelbaumTechnion—Israel Institute of Technology, Haifa, Israel
Chapter 7. Biological formation and reactions of carbonyl groupsFrank Eisenberg Jr.National Institutes of Health, Bethesda, Maryland, U.S.A.
Chapter 8. Chemical and physical methods of analysisJ. Gordon HannaOlin Mathieson Chemical Corp., New Haven, Conn., U.S.A.
Chapter 9. Basicity of carbonyl compoundsV. A. PalmTartu State University, Estonian SSR, USSR
U. L. HaldnaTartu State University, Estonian SSR, USSR
A. J. TalvikTartu State University, Estonian SSR, USSR
Chapter 10. Oxidation of aldehydes by transition metalsJan RocekThe Catholic University of America, Washington, U.S.A.
Chapter 11. Reduction of carbonyl groupsOwen H. WheelerPuerto Rico Nuclear Center, Mayaguez, Puerto Rico
Chapter 12. Condensations leading to double bondsRichard L. ReevesEastman Kodak Company, Rochester, New York, U.S.A.
Chapter 13. Reactions of carbonyl groups with organometallic compoundsTheophil EicherUniversity of Wurzburg, Germany
Chapter 14. DecarbonylationW. M. SchubertUniversity of Washington, U.S.A.Robert Roy KintnerAugustana College, South Dakota, U.S.A.
Chapter 15. Rearrangements involving the carbonyl groupClair J. CollinsOak Ridge National Laboratory and The University of Tennessee, U.S.A.
Jerome F. EasthamThe University of Tennessee, U.S.A.
3
Chapter 16. Photochemistry of ketones and aldehydesJ. N. Pitts Jr.University of California, Riverside, U.S.A.
J. K. S. WanUniversity of California, Riverside, U.S.A.
Chapter 17. ThioketonesE. CampaigneIndiana University, U.S.A.
The Chemistry of Ether Linkage (1967)Edited by Saul Patai
Chapter 1. Theory of the ether linkageDavid PetersRoyal Holloway College, London, England
Chapter 2. Cleavage of the C−O−C bondEberhard StaudeInstitute of Technical Chemistry, Munchen, Germany
Franz PatatInstitute of Technical Chemistry, Munchen, Germany
Chapter 3. Directive and activating effects of alkoxy and aryloxy groups in aromaticand aliphatic reactionsG. KohnstamUniversity of Durham, England
D. L. H. WilliamsUniversity of Durham, England
Chapter 4. The pyrolysis of ethersK. J. LaidlerUniversity of Ottawa, Canada
D. J. McKenneyUniversity of Windsor, Canada
Chapter 5. Biological formations and reactionsKurt WallenfelsDepartment of Biochemistry, University of Freiburg, Germany
Hans DiekmannDepartment of Biochemistry, University of Freiburg, Germany
Chapter 6. Basicity and complexing ability of ethersScott Searles Jr.Department of Chemistry, University of Missouri, U.S.A.
Milton TamresDepartment of Chemistry, University of Michigan, U.S.A.
4
Chapter 7. Acetals and hemiacetalsErnst SchmitzGerman Academy of Sciences, Berlin-Adlershof, G.D.R.
Inge EichhornGerman Academy of Sciences, Berlin-Adlershof, G.D.R.
Chapter 8. Photochemistry of the C−O−C groupDov EladThe Weizmann Institute of Science, Rehovth, Israel
Chapter 9. Reactions of cyclic ethersRoy J. GritterIBM Research Laboratory, San Jose, California, U.S.A.
Chapter 10. Methods of formation of the ether linkageHenry FeuerPurdue University, Lafayette, Indiana, U.S.A.
John HoozUniversity of Alberta, Edmonton, Canada
Chapter 11. The polyethersCharles C. PriceUniversity of Pennsylvania, Philadelphia, U.S.A.
Chapter 12. Interconversion of C−O−C, C−S−C, and C−Se−C groupsVaclav HorakCharles University, Prague, Czechoslovakia
Jurgen GosselckThe University, Giessen, Germany
Chapter 13. The chemistry of thioethers; differences and analogies with ethersL. BrandsmaUniversity of Utrecht, Holland
J. F. ArensUniversity of Utrecht, Holland
Chapter 14. Rearrangements of ethersD. L. DalrympleUniversity of Vermont, U.S.A.
T. L. KrugerUniversity of Vermont, U.S.A.
W. N. WhiteUniversity of Vermont, U.S.A.
Chapter 15. Detection and estimation of ethersJames S. FritzIowa State University, Ames, U.S.A.
Chapter 16. Appendix on safety measuresN. V. SteereUniversity of Minnesota, U.S.A.
5
The Chemistry of the Amino Group (1968)Edited by Saul Patai
Chapter 1. General and theoreticalR. DaudelSorbonne and Centre de Mecanique Ondulatoire Appliquee, Paris, France
Chapter 2. The introduction of the amino groupM. S. GibsonFaculty of Technology, University of Manchester
Chapter 3. Detection, determination, and characterisation of aminesJacob ZabickyInstitute for Fibres and Forest Products Research, Jerusalem, Israel
Chapter 4. Basicity and complex formationJ. W. SmithBedford College, London
Chapter 5. Directing and activating effectsGabriel ChuchaniInstituto Venezolano de Investigaciones Cientıficas, IVIC, Caracas, Venezuela
Chapter 6. Substitution at an amino nitrogenBrian C. ChallisSt. Salvator’s College, University of St. Andrews, Scotland
Anthony R. ButlerSt. Salvator’s College, University of St. Andrews, Scotland
Chapter 7. Carbon—nitrogen and nitrogen—nitrogen double bond condensation reactionsPaula Y. SollenbergerUniversity of Virginia, Charlottesville, Virginia, U.S.A.
R. Bruce MartinUniversity of Virginia, Charlottesville, Virginia, U.S.A.
Chapter 8. Cleavage of the carbon—nitrogen bondEmil H. WhiteDepartment of Chemistry, The Johns Hopkins University, Baltimore, Maryland 21218
David J. WoodcockDepartment of Chemistry, The Johns Hopkins University, Baltimore, Maryland 21218
Chapter 9. Biological formation and reactions of the amino groupBarbara E. C. BanksPhysiology Department, University College, London
Chapter 10. Rearrangements involving amino groupsD. V. BanthorpeUniversity College, London
Chapter 11. Protection of the amino groupY. WolmanDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Israel
6
Chapter 12. TetraaminoethylenesDavid M LemalDartmouth College, Hanover, New Hampshire, U.S.A.
The Chemistry of Carboxylic Acids and Esters (1969)Edited by Saul Patai
Chapter 1. General and theoretical aspects of the COOH and COOR groupsMassimo SimonettaInstitute of Chemical Physics, University of Milan, Italy
Sergio CarraInstitute of Chemical Physics, University of Milan, Italy
Chapter 2. Electrochemical reactions of carboxylic acids and related processesLennart EbersonUniversity of Lund, Sweden
Chapter 3. Alcoholysis, acidolysis and redistribution of estersJouko KoskikallioUniversity of Oulu, Finland
Chapter 4. The formation of carboxylic acids and their derivatives from organometallic compoundsR. P. A. SneedenMonsanto Research S. A., Zurich, Switzerland
Chapter 5. Synthesis of di- and polycarboxylic acids and estersV. F. KucherovN.D. Zelinsky Institute of Organic Chemistry, Academy of Sciences of the U.S.S.R., Moscow, U.S.S.R.
L. A. YanovskayaN.D. Zelinsky Institute of Organic Chemistry, Academy of Sciences of the U.S.S.R., Moscow, U.S.S.R.
Chapter 6. Acidity and hydrogen bonding of carboxyl groupsLennart EbersonUniversity of Lund, Sweden
Chapter 7. Introduction of COOH groups by carbonyl olefinationL. D. BergelsonInstitute for Chemistry of Natural Products, Academy of Sciences of U.S.S.R., Moscow, U.S.S.R.
M. M. ShemyakinInstitute for Chemistry of Natural Products, Academy of Sciences of U.S.S.R., Moscow, U.S.S.R.
Chapter 8. Rearrangement and cyclization reactions of carboxylic acids and estersHarold KwartUniversity of Delaware, Newark, Delaware, U. S. A.
Kenneth KingUniversity of Delaware, Newark, Delaware, U. S. A.
Chapter 9. Substitution in the groups COOH and COORD. P. N. SatchellKing’s College, London, England
7
R. S. SatchellQueen Elizabeth College, London, England
Chapter 10. Syntheses and uses of isotopically labelled carboxylic acidsMieczyslaw ZielinskiUniversity of Warsaw, Poland
Chapter 11. Esterification and ester hydrolysisErkki K. EurantoUniversity of Turku, Finland
Chapter 12. The decarboxylation reactionLouis W. ClarkWestern Carolina University, Cullowhee, North Carolina, U.S.A.
Chapter 13. Ortho estersE. H. CordesIndiana University, Bloomington, Indiana, U.S.A.
Chapter 14. Peracids and perestersSven-Olov LawessonUniversity of Aarhus, Denmark
Gustav SchrollUniversity of Aarhus, Denmark
Chapter 15. Thiolo, thiono and dithio acids and estersMatthys J. JanssenThe University, Groningen, Netherlands
Chapter 16. Directive and activating effects of CO2H and CO2R groups in aromaticand aliphatic reactionsG. KohnstamUniversity of Durham, England
D. L. H. WilliamsUniversity of Durham, England
Chapter 17. Analysis of carboxylic acids and estersT. S. MaCity University of New York, U.S.A.
Chapter 18. Biological formation and reactions of the −COOH and −COOR groupsShawn DoonanUniversity College, London, England
The Chemistry of the Nitro and Nitroso Groups, Part 1 (1969)Edited by Henry Feuer
Chapter 1. Theoretical aspects of the C—NO and C—NO2 bondsGeorge H. WagnierePhysikalisch Chemisches Institut, University of Zurich, Zurich, Switzerland
8
Chapter 2. Spectoscopy of the nitro groupC. N. R. RaoDepartment of Chemistry, Indian Institute of Technology, Kanpur, India
Chapter 3. Spectroscopy of the nitroso groupC. N. R. Rao and K. R. BhaskarDepartment of Chemistry, Indian Institute of Technology, Kanpur, India
Chapter 4. The photochemistry of the nitro and nitroso groupsHenry A. MorrisonDepartment of Chemistry, Purdue University, West Lafayette, Indiana, USA
Chapter 5. Methods of formation of the nitroso groups and its reactionsJ. H. BoyerChicago Circle Campus, University of Illinois, Chicago, Illinois, USA
Chapter 6. Methods of formation of the nitro group in aliphatic and alicyclic systemsH. O. LarsonDepartment of Chemistry, University of Hawaii, Honolulu, Hawaii
Chapter 7. Nitronic acids and estersArnold T. NielsenMichelson Laboratory, Naval Weapons Center, China Lake, California, USA
Chapter 8. Activating effects of the nitro group in nucleophilic aromatic substitutionsTh. J. de Boer and I. P. DirkxOrganic Chemistry Laboratory, University of Amsterdam, The Netherlands
Chapter 9. Methods of formation of the nitramino group, its properties and reactionsGeorge F. WrightUniversity of Toronto, Toronto, Ontario, Canada
The Chemistry of Alkenes, Volume 2 (1970) (See Volume 1 in 1964)
Edited by Jacob Zabicky
Chapter 1. Nuclear Magnetic Resonance Spectra of AlkenesV. S. WattsEmory University, Atlanta, Georgia, U.S.A.
J. H. GoldsteinEmory University, Atlanta, Georgia, U.S.A.
Chapter 2. The Properties of Alkene Carbonium Ions and CarbanionsHerman G. Richey Jr.The Pennsylvania State University, University Park, Pennsylvania, U.S.A.
Chapter 3. Alkene RearrangementsKenneth MackenzieUniversity of Bristol, England
9
Chapter 4. Hydrogenation of AlkenesSekio MitsuiTohoku University, Sendai, Japan
Akira KasaharaYamagata University, Yamagata, Japan
Chapter 5. Alkene Complexes of Transition Metals as Reactive IntermediatesJean-Francois BiellmannFaculte des Sciences, Strasbourg, France
Henri HemmerSociete Nationale des Petroles d’Aquitaine, Lacq, France
Jacques LevisallesFaculte des Sciences, Nancy, France
Chapter 6. Photochemistry of OlefinsK. J. CrowleyTrinity College, Dublin, Ireland
P. H. MazzocchiUniversity of Maryland, College Park, Maryland, U.S.A.
Chapter 7. The Mass Spectrometry of the Double BondA. G. LoudonUniversity College, London, England
Allan MaccollUniversity College, London, England
Chapter 8. The Radiolysis of OlefinsG. G. MeiselsDepartment of Chemistry, University of Houston, Texas, U.S.A.
Chapter 9. Polymers containing C−C bondsMorton A. GolubStanford Research Institute, Menlo Park, California, U.S.A.
Chapter 10. Olefinic Properties of CyclopropanesMarvin ChartonPratt Institute, Brooklyn, N.Y., U.S.A.
The Chemistry of Amides (1970)Edited by Jacob Zabicky
Chapter 1. Molecular and electronic structure of the amide groupM. B. RobinBell Telephone Laboratories, Incorporated, Murray Hill, New Jersey, U.S.A.
F. A. BoveyBell Telephone Laboratories, Incorporated, Murray Hill, New Jersey, U.S.A.
Harold BaschBell Telephone Laboratories, Incorporated, Murray Hill, New Jersey, U.S.A.
10
Chapter 2. Synthesis of amidesA. L. J. BeckwithUniversity of Adelaide, Australia
Chapter 3. Acid-base and complexing properties of amidesR. B. HomerSchool of Chemical Sciences, University of East Anglia, Norwich, England
C. D. JohnsonSchool of Chemical Sciences, University of East Anglia, Norwich, England
Chapter 4. Rearrangement and elimination of the amido groupJoseph F. BieronCanisius College, Buffalo, New York, U.S.A.
Frank J. DinanCanisius College, Buffalo, New York, U.S.A.
Chapter 5. Photochemistry of the amido groupIonel RosenthalDepartment of Chemistry, The Weizmann Institute of Science, Rehovoth, Israel
Chapter 6. Radiation chemistry of amidesOwen H. WheelerPuerto Rico Nuclear Centre, Mayaguez, Puerto Rico
Chapter 7. Chemistry of imidic compoundsOwen H. WheelerPuerto Rico Nuclear Center, Mayaguez, Puerto Rico
Oscar RosadoUniversity of Puerto Rico at Mayaguez, Puerto Rico
Chapter 8. The chemistry of thioamidesW. WalterUniversity of Hamburg, Germany
J. VossUniversity of Hamburg, Germany
Chapter 9. The chemistry of the thiohydrazide groupW. WalterUniversity of Hamburg, Germany
K. J. ReubkeUniversity of Hamburg, Germany
Chapter 10. The chemistry of hydrazidesHans PaulsenUniversity of Hamburg, Germany
Dieter StoyeUniversity of Hamburg, Germany
Chapter 11. Biological formation and reactions of the amido groupJ. E. ReimannMichigan State University, East Lansing, Michigan, U.S.A.
11
R. U. ByerrumMichigan State University, East Lansing, Michigan, U.S.A.
Chapter 12. Directing and activating effects of the amido groupJ. A. ShaferThe University of Michigan, Ann Arbor, Michigan, U.S.A.
Chapter 13. Reactions of the carboxamide groupBrian G. ChallisImperial College, London, England
Judith A. ChallisImperial College, London, England
The Chemistry of the Carbon–Nitrogen Double Bonds (1970)Edited by Saul Patai
Chapter 1. General and theoretical aspectsC. SandorfyUniversite de Montreal, Canada
Chapter 2. Methods of formation of the carbon-nitrogen double bondShlomo DayagiTel-Aviv University, Israel
Yair DeganiWeizmann Institute of Science, Rehovoth, Israel
Chapter 3. Analysis of azomethinesDavid J.CurranUniversity of Massachusetts, Amherst, Massachusetts, U.S.A.
Sidney SiggiaUniversity of Massachusetts, Amherst, Massachusetts, U.S.A.
Chapter 4. The optical rotatory dispersion and circular dichroism of azomethiniesR. BonnettQueen Mary College, London, England
Chapter 5. Basic and complex-forming propertiesJ. W. SmithBedford College, London, England
Chapter 6. Additions to the azomethine groupKarou HaradaUniversity of Miami, Florida, U.S.A.
Chapter 7. Cycloaddition reactions of carbon–nitrogen double bondsJean-Pierre AnselmeUniversity of Massachusetts, Boston, U.S.A.
Chapter 8. Substitution reactions at the azomethine carbon and nitrogen atomsR. J. MorathCollege of St. Thomas, St. Paul, Minnesota, U.S.A.
12
Gardner W. StacyWashington State University, Pullman, Washington, U.S.A.
Chapter 9. syn-anti Isomerizations and rearrangementsC. G. McCartyWest Virginia University, Morgantown, U.S.A.
Chapter 10. Cleavage of the carbon–nitrogen double bondAlbert BruylantsUniversite de Louvain, Belgium
E. Feytmants-de MedicisUniversite de Louvain, Belgium
Chapter 11. Electrochemistry of the carbon–nitrogen double bondHenning LundUniversity of Aarhus, Denmark
Chapter 12. Photochemistry of the carbon-nitrogen double bondGunnar WettermarkInstitute of Physical Chemistry, University of Uppsala, Sweden
Chapter 13. Imidoyl halidesR. BonnettQueen Mary College, London, England
Chapter 14. Quinonediimines and related compoundsK. Thomas FinleyEastman Kodak Company, Rochester, New York, U.S.A.
L. K. J. TongEastman Kodak Company, Rochester, New York, U.S.A.
The Chemistry of the Carbonyl Group, Volume 2 (1970) (See Volume 1 in 1966)
Edited by Jacob Zabicky
Chapter 1. Equilibrium additions to carbonyl compoundsYoshiro OgataNagoya University, Chikusa-ku, Nagoya, Japan
Atsushi KawasakiNagoya University, Chikusa-ku, Nagoya, Japan
Chapter 2. Oxidation of aldehydes and ketonesHerbert S. VerterInter-American University of Puerto Rico, San German, and the Puerto Rico Nuclear Centre, Mayaguez,Puerto Rico
Chapter 3. EnolizationS. ForsenThe Royal Institute of Technology, S-10044 Stockholm, Sweden
M. NilssonThe Royal Institute of Technology, S-10044 Stockholm, Sweden
13
Chapter 4. Oxocarbons and their reactionsRobert WestThe University of Wisconsin, Madison, Wisconsin, U.S.A.
Joseph NiuWyandotte Chemical Corporation, Wyandotte, Michigan, U.S.A.
Chapter 5. Mass spectrometry of carbonyl compoundsJ. H. BowieThe University of Adelaide, South Australia
Chapter 6. Radiation chemistry of ketones and aldehydesGordon R. FreemanUniversity of Alberta, Edmonton, Alberta, Canada
The Chemistry of the Cyano Group (1970)Edited by Zvi Rappoport
Chapter 1. Electronic structure in molecules, especially in cyano compoundsE. ClementiIBM Research Laboratory, San Jose, California, U.S.A.
Chapter 2. Introduction of the cyano group into the moleculeKlaus FriedrichUniversity of Freiburg, Freiburg/Br., Germany
Kurt WallenfelsUniversity of Freiburg, Freiburg/Br., Germany
Chapter 3. Basicity, hydrogen bonding and complex formationJust GrundnesUniversity of Oslo, Oslo, Norway
Peter KlaboeUniversity of Oslo, Oslo, Norway
Chapter 4. Detection and determination of nitrilesDavid J. CurranUniversity of Massachusetts, Amherst, Massachusetts, U.S.A.
Sidney SiggiaUniversity of Massachusetts, Amherst, Massachusetts, U.S.A.
Chapter 5. Directing and activating effects of the cyano groupWilliam A. SheppardE. I. du Pont de Nemours and Co. Wilmington, Delaware, U.S.A.
Chapter 6. Nitrile reactivityFred C. SchaeferAmerican Cyanamid Co., Stamford, Conn., U.S.A.
Chapter 7. Reduction of the cyano groupMordecai RabinovitzThe Hebrew University of Jerusalem, Jerusalem, Israel
14
Chapter 8. Additions to the cyano group to form heterocyclesA. I. MeyersLouisiana State University in New Orleans, New Orleans, Louisiana, U.S.A.
J. C. SircarLouisiana State University in New Orleans, New Orleans, Louisiana, U.S.A.
Chapter 9. Cyanocarbon and polycyano compoundsE. CiganekE. I. du Pont de Nemours and Co. Wilmington, Delaware, U.S.A.
W. J. LinnE. I. du Pont de Nemours and Co. Wilmington, Delaware, U.S.A.
O. W. WebsterE. I. du Pont de Nemours and Co. Wilmington, Delaware, U.S.A.
Chapter 10. Molecular complexes of polycyano compoundsL. Russell MelbyE. I. du Pont de Nemours and Co. Wilmington, Delaware, U.S.A.
Chapter 11. Radicals with cyano groupsH. D. HartzlerE. I. du Pont de Nemours and Co. Wilmington, Delaware, U.S.A.
Chapter 12. The biological function and formation of the cyano groupJ. P. FerrisRensselaer Polytechnic Institute, Troy, New York, U.S.A.
Chapter 13. Syntheses and uses of isotopically labelled cyanidesLouis PichatLabelled Compounds Division C.E.N.-Saclay, Gif-sur-Yvette (91), France
Chapter 14. Nitrile oxidesCh. GrundmannMellon Institute, Carnegie-Mellon University Pittsburgh, Pa., U.S.A.
Chapter 15. IsonitrilesPeter HoffmannBayer A.G., Leverkusen, W. Germany and University of Southern California, Los Angeles
Dieter MarquardingBayer A.G., Leverkusen, W. Germany and University of Southern California, Los Angeles
Helmut KliimannBayer A.G., Leverkusen, W. Germany and University of Southern California, Los Angeles
Ivar UgiBayer A.G., Leverkusen, W. Germany and University of Southern California, Los Angeles
Chapter 16. Rearrangement reactions involving the cyano groupJoseph Casanova Jr.California State College, Los Angeles, California, U.S.A.
15
The Chemistry of the Nitro and Nitroso Groups, Part 2 (1970)Edited by Henry Feuer
Chapter 1. Introduction of the nitro group into aromatic systemsWilliam M. WeaverDepartment of Chemistry, John Carroll University, Cleveland, Ohio
Chapter 2. Directing effects of the nitro group in electrophilic and radical aromatic substitutionsTadeusz UrbanskiWarsaw Institute of Technology (Politechnika), Warszawa, Poland
Chapter 3. Activating and directing effects of the nitro group in aliphatic systemsHans H. BaerDepartment of Chemistry, University of Ottawa, Ottawa, Ontario, Canada
Ljerka UrbasDepartment of Chemistry, University of Ottawa, Ottawa, Ontario, Canada
Chapter 4. Biochemistry and Pharmacology of the Nitro and Nitroso GroupsJan VenuletDrug Research Institute, Warsaw, Poland
Robert L. Van EttenDepartment of Chemistry, Purdue University, Lafayette, Indiana
Chapter 5. The synthesis and reactions of trinitromethyl compoundsLloyd A. KaplanChemistry Research Department, U.S. Naval Ordnance Laboratory, Silver Spring, Maryland
Chapter 6. Polynitroaromatic addition compoundsThomas N. HallU.S. Naval Ordnance Laboratory, White Oak Silver Spring, Maryland
Chester F. Poranski Jr.U.S. Naval Research Laboratory Washington, D.C.
The Chemistry of the Azido Group (1971)Edited by Saul Patai
Chapter 1. General and theoretical aspectsA. TreininThe Hebrew University, Jerusalem, Israel
Chapter 2. Introduction of the Azido GroupM. E. C. BiffinDefence Standards Laboratories, Maribyrnong, Victoria, Australia
J. MillerUniversity of Natal, Durban, S. Africa
D. B. PaulDefence Standards Laboratories, Maribyrnong, Victoria, Australia
16
Chapter 3. Characterization and determination of organic azidesJerome E. GurstDepartment of Chemistry, University of West Florida, Pensacola, Florida
Chapter 4. The directing and activating effects of the azido groupM. E. C. BiffinDefence Standards Laboratories, Maribyrnong, Victoria, Australia
J. MillerUniversity of Natal, Durban, S. Africa
D. B. PaulDefence Standards Laboratories, Maribyrnong, Victoria, Australia
Chapter 5. Decomposition of organic azidesR. A. AbramovitchUniversity of Alabama, University, Alabama 35486
E. P. KybaUniversity of Alabama, University, Alabama 35486
Chapter 6. Abides as synthetic starting materialsTuvia SheradskyThe Hebrew University, Jerusalem, Israel
Chapter 7. Rearrangements involving azido groupsD. V. BanthorpeUniversity College, London
Chapter 8. Photochemistry of the azido groupA. ReiserResearch Laboratory, Kodak Limited, Harrow, Middlesex, England
Wagner H. M.Research Laboratory, Kodak Limited, Harrow, Middlesex, England
Chapter 9. Acyl azidesWalter LwowskiNew Mexico State University, Las Cruces, New Mexico, U.S.A.
Chapter 10. The chemistry of vinyl azidesGerald SmolinskyBell Telephone Laboratories, Murray Hill, New Jersey, U.S.A.
Goralie A. PrydeBell Telephone Laboratories, Murray Hill, New Jersey, U.S.A.
The Chemistry of the Hydroxyl Group, Part 1 (1971)Edited by Saul Patai
Chapter 1. Theoretical aspects of the chemistry of the hydroxyl groupR. F. W. BaderDepartment of Chemistry, McMaster University, Hamilton, Ontario, Canada
17
Chapter 2. Nucleophilic attack by hydroxide and alkoxide ionsColin A. FyfeUniversity of Guelph, Guelph, Ontario, Canada
Chapter 3. Free radical and electrophilic hydroxylationD. F. SangsterA.A.E.C. Research Establishment, Sutherland, New South Wales, Australia
Chapter 4. Formation of hydroxyl groups via oxymetallation, oxidation, and reductionI. R. L. BarkerBrighton College of Technology, Sussex, England
Chapter 5. Electrochemistry of the hydroxyl groupHenning LundDepartment of Chemistry, University of Aarhus, 8000 Aarhus C, Denmark
Chapter 6. Detection and determination of hydroxyl groupsSidney SiggiaUniversity of Massachusetts, Amherst, Massachusetts, U.S.A.
J. Gordon HannaConnecticut Agricultural Experiment Station, New Haven, Connecticut, U.S.A.
Thomas R. StengleUniversity of Massachusetts, Amherst, Massachusetts, U.S.A.
Chapter 7. Acidity and inter- and intra-molecular H-bondsC. H. RochesterNottingham University, England
Chapter 8. Directing and activating effectsD. A. R. HapperUniversity of Canterbury, Christchurch, New Zealand
J. VaughanUniversity of Canterbury, Christchurch, New Zealand
Chapter 9. Electrophilic attacks on the hydroxyl groupPentti SalomaaDepartment of Chemistry, University of Turku, Turku, Finland
Alpo KankaanperaDepartment of Chemistry, University of Turku, Turku, Finland
Kalevi PihlajaDepartment of Chemistry, University of Turku, Turku, Finland
Chapter 10. Oxidation and reduction of phenolsMihailo Lj. MihailovicDepartment of Chemistry, Faculty of Sciences, University of Belgrade and Institute for Chemistry,Technology and Metallurgy, Belgrade, Yugoslavia
Zivorad CekovicDepartment of Chemistry, Faculty of Sciences, University of Belgrade and Institute for Chemistry,Technology and Metallurgy, Belgrade, Yugoslavia
18
Chapter 11. Displacement of hydroxyl groupsGeoffrey W. BrownSir John Cass College, London, England
Chapter 12. The dehydration of alcoholsH. KnozingerInstitute of Physical Chemistry, The University of Munich, Germany
Chapter 13. Uncatalysed rearrangements involving the hydroxyl groupElliot N. MarvellOregon State University, Corvallis, Oregon, U.S.A.
William WhalleyOregon State University, Corvallis, Oregon, U.S.A.
Chapter 14. Biological formation and reactions of the hydroxyl groupS. K. EricksonUniversity of Leicester, Leicester, England
J. SchadelinJustus Liebig Universitat, 63 Giessen, Germany
U. SchmelingJustus Liebig Universitat, 63 Giessen, Germany
H.-H. SchottJustus Liebig Universitat, 63 Giessen, Germany
V. UllrichJustus Liebig Universitat, 63 Giessen, Germany
Hj. StaudingerJustus Liebig Universitat, 63 Giessen, Germany
Chapter 15. Syntheses and uses of 18O-labelled hydroxylic compoundsS. OaeOsaka City University, Osaka, Japan
S. TamagakiOsaka City University, Osaka, Japan
Chapter 16. Photochemistry of alcohols and phenolsHans-Dieter BeckerGeneral Electric Research and Development Center, Schenectady, New York, U.S.A.
Chapter 17. The radiation chemistry of the hydroxyl groupR. A. BassonAtomic Energy Board, Pretoria, Republic of South Africa
Chapter 18. Protection of the hydroxyl groupH. M. FlowersDepartment of Biophysics, The Weizmann Institute of Science, Rehovoth, Israel
Chapter 19. The mass spectra of hydroxyl compoundsR. Graham CooksDepartment of Chemistry, Kansas State University, Manhattan, Kansas 66502, U.S.A.
19
Chapter 20. Hydroxide-alkoxide ion equilibria and their influence on chemical reactionsJuhani MurtoDepartment of Chemistry, University of Helsinki, Helsinki 17, Finland
The Chemistry of Acyl Halides (1972)Edited by Saul Patai
Chapter 1. General and theoretical aspectsMassimo SimonettaIstituto di Chimica fisica, Universita, Milano, Italy
Paolo BeltrameIstituto Chimico, Universita, Cagliari, Italy
Chapter 2. Preparation of acyl halidesMartin F. AnsellQueen Mary College, (University of London), England
Chapter 3. Detection, determination and characterizationHannah Weiler-FeilchenfeldDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Israel
Chapter 4. Acid-base behaviour and complex formationD. P. N. SatchellKing’s College, London, England
R. S. SatchellQueen Elizabeth College, London, England
Chapter 5. Directing and activating effects of COX groupsP. H. GoreBrunel University, Uxbridge, Middlesex, England
Chapter 6. Mechanisms of substitution at the COX groupAntti KivinenUniversity of Helsinki, Finland
Chapter 7. ReductionOwen H. WheelerCaribbean Research Laboratories, Omni Research Inc., Mayaguez, Puerto Rico
Chapter 8. Rearrangements involving acyl halidesD. V. BanthorpeUniversity College, London
B. V. SmithChelsea College of Science and Technology, University of London
Chapter 9. Photochemistry and radiation chemistry of carbonyl halidesU. SchmidtOrganisch-chemisches Institut, University of Vienna, Austria
H. EggerSandoz Forschungsinstitut, Vienna, Austria
20
Chapter 10. Biological reactions of carbonyl halidesSasson CohenIsrael Institute for Biological Research, Ness-Ziona, Israel
Chapter 11. Thiocarbonyl halidesK. T. PottsRensselaer Polytechnic Institute, Troy, New York
C. SapinoRensselaer Polytechnic Institute, Troy, New York
Chapter 12. Chloroformate esters and related compoundsDennis N. KevillDepartment of Chemistry, Northern Illinois University, DeKalb, Illinois, 60115
Chapter 13. The acyl hypohalitesDennis D. TannerUniversity of Alberta, Edmonton, Alberta, Canada
Nigel J. BunceUniversity of Guelph, Guelph, Ontario, Canada
The Chemistry of the Carbon—Halogen Bond, Part 1 (1973)Edited by Saul Patai
Chapter 1. General and theoretical aspects of the carbon—halogen bondGeorges H. WagnierePhysikalisch-Chemisches Institut, University of Zurich, Zurich, Switzerland
Chapter 2. Structural chemistry of the C−X bondJ. TrotterUniversity of British Columbia, Vancouver, Canada
Chapter 3. Analysis of organic halogen compoundsJacob ZabickyThe Weizmann Institute of Science, Rehovot, Israel
Sarah Ehrlich-RogozinskiThe Weizmann Institute of Science, Rehovot, Israel
Chapter 4. Mass spectrometry and the carbon-halogen bondA. G. LoudonChristopher Ingold Laboratories, University College, London, England
Chapter 5. Hydrogen-bonding and complex-forming propertiesJ. W. SmithDepartment of Chemistry, Bedford College, University of London, England
Chapter 6. Directing, activating and deactivating effectsG. ModenaCentro CNR ‘Meccanismi di Reazioni Organiche’, Istituto di Chimica Organica, Padova, Italy
G. ScorranoCentro CNR ‘Meccanismi di Reazioni Organiche’, Istituto di Chimica Organica, Padova, Italy
21
Chapter 7. Heterolytic mechanisms of substitution involving carbon-halogen bondsP. B. D. de la MareChemistry Department, University of Auckland, Auckland, New Zealand
B. E. SwedlundChemistry Department, University of Auckland, Auckland, New Zealand
Chapter 8. Homolytic mechanisms of substitutionEarl S. HuyserUniversity of Kansas, Lawrence, Kansas 66044, U.S.A.
Chapter 9. Elimination reactions in solutionR. A. More O’FerrallDepartment of Chemistry, University College, Dublin 4, Ireland
Chapter 10. Pyrolysis reactions involving carbon–halogen bondsKurt W. EggerMonsanto Research S.A., 8050 Zurich, Switzerland
Alan T. CocksMonsanto Research S.A., 8050 Zurich, Switzerland
Chapter 11. Photochemistry of the C−X groupP. G. SammesChemistry Department, Imperial College, London, England
Chapter 12. Radiation chemistry of the carbon–halogen bondRolf E. BuhlerSwiss Federal Institute of Technology, Zurich, Switzerland
Chapter 13. The biochemistry of carbon–halogen compoundsShawn DoonanUniversity College, London, England
Chapter 14. Perchloro-, perbromo- and periodo-compoundsT. ChiversThe University of Calgary, Calgary, Alberta, Canada
Chapter 15. Electrochemistry of the carbon–halogen bondJoseph CasanovaCalifornia State University, Los Angeles, California, U.S.A.
Lennart EbersonChemical Center, University of Lund, Lund, Sweden
Chapter 16. Thermochemistry of organic halidesRobert ShawPhysical Sciences Division, Stanford Research Institute, Menlo Park, California 94025, U.S.A.
Chapter 17. Rearrangements involving halidesC. RappeDepartment of Chemistry, University of Umea, S-901 87 Umea, Sweden
22
The Chemistry of Quinonoid Compounds, Volume 1, Part 1 (1974) (See Volume 2 in 1988)
Edited by Saul Patai
Chapter 1. Theoretical and general aspectsGerald Jay GleicherDepartment of Chemistry, Oregon State University, Corvallis, Oregon, U.S.A. 97331
Chapter 2. The structural chemistry of quinonesJ. BernsteinUniversity of the Negev, Beersheba, Israel
M. D. CohenWeizmann Institute of Science, Rehovot, Israel
L. LeiserowitzWeizmann Institute of Science, Rehovot, Israel
Chapter 3. SynthesisR. H. ThomsonDepartment of Chemistry, University of Aberdeen, Scotland
Chapter 4. Identification and determination of quinonesSt. BergerChemisches Institut der Universitat Tubingen, D-74 Tubingen, Germany
A. RiekerChemisches Institut der Universitat Tubingen, D-74 Tubingen, Germany
Chapter 5. Mass spectra of quinonesKlaus-Peter ZellerChemisches Institut der Universitat Tubingen, D-74 Tubingen, Germany
Chapter 6. Quinone complexesR. FosterChemistry Department, University of Dundee, Dundee, Scotland
M. I. ForemanDepartment of Pure and Applied Chemistry, University of Strathclyde, Glasgow, Scotland
Chapter 7. Quinones as oxidants and dehydrogenating agentsHans-Dieter BeckerDepartment of Organic Chemistry, Chalmers University of Technology and University of Gothenburg,S-402 20 Gothenburg 5, Sweden
Chapter 8. Rearrangements of quinonesHarold W. MooreUniversity of California, Irvine, California, U.S.A.
Ronald J. WikholmUniversity of California, Irvine, California, U.S.A.
Chapter 9. Photochemistry of quinonesJ. Malcolm BruceDepartment of Chemistry, The University, Manchester M13 9PL, England
23
Chapter 10. Radiation chemistry of quinonesJ. H. FendlerDepartment of Chemistry, Texas A and M University, College Station, Texas 77843, U.S.A.
E. J. FendlerDepartment of Chemistry, Texas A and M University, College Station, Texas 77843, U.S.A.
Chapter 11. Fragmentation reactions of quinonesP. HodgeDepartment of Chemistry, University of Lancaster, Lancashire, England
Chapter 12. Syntheses and uses of isotopically labelled quinonesMieczyslaw ZielinskiInstitute of Chemistry of the Jagiellonian University of Cracow, Poland
Chapter 13. Biological reactions of qyinonesRonald BentleyDepartment of Biochemistry, F.A.S., University of Pittsburgh, Pittsburgh, U.S.A.
Iain M. CampbellDepartment of Biochemistry, F.A.S., University of Pittsburgh, Pittsburgh, U.S.A.
Chapter 14. Electrochemistry of quinonesJames Q. ChambersDepartment of Chemistry, University of Tennessee, Knoxville, Tennessee, 37916, U.S.A.
Chapter 15. Polymeric quinonesA. S. LindseyNational Physical Laboratory, Teddington, Middlesex, England
Chapter 16. Non-benzenoid quinonesT. A. TurneyChemistry Department, University of Auckland, Auckland, New Zealand
Chapter 17. The addition and substitution chemistry of quinonesK. Thomas FinleyDepartment of Chemistry, State University College, Brockport, New York 14420, U.S.A.
Chapter 18. Quinone methidesH.-U. WagnerInstitut fur Organische Chemie der Universitat Munchen, Karlstrasse 23, 8 Munich 2, Germany
R. GompperInstitut fur Organische Chemie der Universitat Munchen, Karlstrasse 23, 8 Munich 2, Germany
The Chemistry of the Thiol Group, Part 1 (1974)Edited by Saul Patai
Chapter 1. General and theoretical aspects of the thiol groupI. G. CsizmadiaLash Miller Chemical Laboratories, Department of Chemistry, University of Toronto, Toronto, Ontario,Canada M 5S 1A1
24
Chapter 2. Structural chemistry of the thiol groupIain C. PaulDepartment of Chemistry, School of Chemical Sciences, University of Illinois, Urbana, Illinois61801, U.S.A.
Chapter 3. Thermochemistry of thiolsRobert ShawPhysical Sciences Division, Stanford Research Institute, Menh Park, California 94025, U.S.A.
Chapter 4. Preparation of thiolsJ. L. WardellDepartment of Chemistry, University of Aberdeen, Meston Walk, Old Aberdeen, AB9 2UE
Chapter 5. Detection and determination of thiolsAngelo FontanaInstitute of Organic Chemistry, University of Padova, Padova, Italy
Claudio TonioloInstitute of Organic Chemistry, University of Padova, Padova, Italy
Chapter 6. The mass spectra of thiolsChava LifshitzDepartment of Physical Chemistry, The Hebrew University of Jerusalem, Israel
Zeev V. ZaretskiiDepartment of Organic Chemistry, The Weizmann Institute of Science, Rehovot, Israel
Chapter 7. The optical rotatory dispersion and circular dichroism of thiolsC. TonioloUniversity of Padova, Padova, Italy
A. FontanaUniversity of Padova, Padova, Italy
Chapter 8. Acidity and hydrogen-bondingM. R. CramptonDurham University, England
Chapter 9. Directing and activating effectsG. MaccagnaniLaboratorio C.N.R. dei Composti del Carbonio contenenti Eteroatomi, Istituto di Chimica Organica,Universita, Bologna, Italy
G. MazzantiLaboratorio C.N.R. dei Composti del Carbonio contenenti Eteroatomi, Istituto di Chimica Organica,Universita, Bologna, Italy
Chapter 10. Photochemistry of thiolsA. R. KnightDepartment of Chemistry and Chemical Engineering, University of Saskatchewan, Saskatoon,Saskatchewan, Canada
Chapter 11. The radiation chemistry of thiolsJ. E. PackerChemistry Department, University of Auckland, Auckland, New Zealand
25
Chapter 12. Synthetic uses of thiolsRichard K. OlsenDepartment of Chemistry and Biochemistry, Utah State University, Logan, Utah 84321
James O. Currie Jr.Department of Chemistry, Pacific University, Forest Grove, Oregon 97116
Chapter 13. Biochemistry of the thiol groupArvan L. FluhartyResearch Specialist, Pacific-Neuropsychiatric Institute Research Program, Pacific State Hospital, Pomona,California,and Adjunct Professor of Biochemistry, University of Southern California School of Medicine, LosAngeles, California
Chapter 14. Protection of the thiol groupY. WolmanDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem, Israel
Chapter 15. Rearrangements involving thiolsTuvia SheradskyThe Hebrew University, Jerusalem, Israel
Chapter 16. Thiols as nucleophilesMichael E. PeachDepartment of Chemistry, Acadia University, Wolfville, Nova Scotia, Canada
Chapter 17. Oxidation of thiolsG. CapozziCentro Meccanismi di Reazioni Organiche, C.N.R., Istituto di Chimica Organica, Universita diPadova, Italy
G. ModenaCentro Meccanismi di Reazioni Organiche, C.N.R., Istituto di Chimica Organica, Universita diPadova, Italy
Chapter 18. The synthesis and uses of isotopieally labelled thiolsAviva LapidotIsotopes Department, Weizmann Institute, Rehovot, Israel
Charles S. IrvingIsotopes Department, Weizmann Institute, Rehovot, Israel
The Chemistry of Amidines and Imidates, Volume 1 (1975) (See Volume 2 in 1991)
Edited by Saul Patai
Chapter 1. General and theoretical aspects of amidines and imidic acid derivativesG. HafelingerUniversitat Tubingen, Germany
Chapter 2. Constitution, configurational and conformational aspects, and chiroptical properties ofimidic acid derivativesG. FodorDepartment of Chemistry, West Virginia University, Morgantown, West Virginia 26506, U.S.A.
26
B. A. PhillipsDepartment of Chemistry, West Virginia University, Morgantown, West Virginia 26506, U.S.A.
Chapter 3. Detection and determination of imidic acid derivativesW. H. PrichardThe City University, London, England
Chapter 4. Rearrangements involving imidsc acid derivativesC. G. McCartyWest Virginia University, Morgantown, U.S.A.
L. A. GarnerWest Virginia University, Morgantown, U.S.A.
Chapter 5. The electrochemistry of Imsdic esters and amidinesHenning LundUniversity of Aarhus, Denmark
Chapter 6. Biological reactions and pharmaceutical uses of imidic acid derivativesRaymond J. GroutDepartment of Pharmacy, The University, Nottingham, England
Chapter 7. Preparation and synthetic uses of amidinesJean-Albert GautierU.E.R. de Chimie Therapeutique, Universite Paris XI, France
Marcel MiocqueU.E.R. de Chimie Therapeutique, Universite Paris XI, France
Claude Combet FarnouxU.E.R. de Chimie Therapeutique, Universite Paris XI, France
Chapter 8. Kinetics and mechanisms of reactions of amidinesRobert H. de WolfeUniversity of California at Santa Barbara, U.S.A.
Chapter 9. Imidates including cyclic imidatesDouglas G. NeilsonChemistry Department, The University, Dundee, Scotland
Chapter 10. The chemistry of amidrazonesK. M. WatsonChemistry Department, The University, Dundee, Scotland
D. G. NeilsonChemistry Department, The University, Dundee, Scotland
Chapter 11. Estimation of the thermochemistry of imidic acid derivativesRobert ShawPhysical Sciences Division, Stanford Research Institute, Menlo Park, California, 94025, U.S.A.
Chapter 12. Complex formation, H-bonding and basicity of imidic acid derivativesJ. SevcıkDepartment of Physical Chemistry. Palacky University, Olomouc, CSSR
F. GrambalDepartment of Physical Chemistry. Palacky University, Olomouc, CSSR
27
The Chemistry of Hydrazo, Azo and Azoxy Groups, Volume 1, Part 1 (1975)(See Volume 2 in 1997)
Edited by Saul Patai
Chapter 1. Electronic Structures of the Azo, Azoxy and Hydrazo GroupsM. B. RobinBell Laboratories, Murray Hill, New Jersey, U.S.A.
Chapter 2. Structural ChemistryR. AllmannPhilipps-Universitat, Lahnberge, 355 Marburg, Germany
Chapter 3. Thermochemistry of Hydrazo, Azo and Azoxy GroupsRobert ShawPhysical Sciences Division, Stanford Research Institute, Menlo Park, California, U.S.A.
Chapter 4. Preparative ProceduresJ. W. TimberlakeLouisiana State University in New Orleans, New Orleans, Louisiana, U.S.A.
J. C. StowellLouisiana State University in New Orleans, New Orleans, Louisiana, U.S.A.
Chapter 5. Mass Spectra of Hydrazo, Azo and Azoxy CompoundsS. W. TamDepartment of Chemistry, Chung Chi College, The Chinese University of Hong Kong, Shatin, N.T.,Hong Kong
Chapter 6. Chiroptical Properties of the Azo and the Azoxy ChromophoresG. SnatzkeLehrstuhl fur Strukturchemie, Ruhr-Universitat, Bochum, Germany
F. SnatzkeLehrstuhl fur Strukturchemie, Ruhr-Universitat, Bochum, Germany
Chapter 7. Basicity, Hydrogen Bonding and Complex Formation Involving Hydrazo, Azo andAzoxy GroupsP. J. KruegerUniversity of Calgary, Calgary, Alberta, Canada, T2N 1N4
Chapter 8. Directing and Activating EffectsD. A. R. HapperUniversity of Canterbury, Christchurch, New Zealand
J. VaughanUniversity of Canterbury, Christchurch, New Zealand
Chapter 9. The Transition Metal Chemistry of Azo CompoundsM. I. BruceDepartment of Inorganic Chemistry, The University, Bristol, England
B. L. GoodallDepartment of Inorganic Chemistry, The University, Bristol, England
28
Chapter 10. Radiation Chemistry of Hydrazo and Azo CompoundsA. HorowitzSoreq Nuclear Research Centre, Yavne, Israel
L. A. RajbenbachSoreq Nuclear Research Centre, Yavne, Israel
Chapter 11. Formation and Fragmentation of Cyclic Azo CompoundsKenneth MackenzieUniversity of Bristol, Bristol, England
Chapter 12. The Electrochemistry of Azoxy, Azo and Hydrazo CompoundsF. G. ThomasChemistry Department, James Cook University of North Queensland, Townsville, Australia, 4811
K. G. BotoElectrochemistry Group, Defence Standards Laboratories, Ascot Vale, Australia, 3032
Chapter 13. Biological Formation and Reactions of Hydrazo, Azo and Azoxy GroupsTetsuo MiyaderaCentral Research Laboratories, Sankyo Co., Ltd., Tokyo, Japan
Chapter 14. Oxidation and Synthetic Uses of Hydrazo, Azo and Azoxy CompoundsBrian T. NewboldDepartement de Chimie, Universite de Moncton, Moncton, New Brunswick, Canada
Chapter 15. Reduction and Synthetic Uses of Hydrazo, Azo and Azoxy CompoundsBrian T. NewboldDepartement de Chimie, Universite de Moncton Moncton, New Brunswick, Canada
Chapter 16. Ionic Reactions Involving Hydrazo, Azo and Azoxy GroupsA. F. HegartyChemistry Department, University College, Cork, Ireland
Chapter 17. Syntheses and Uses of Isotopically Labelled Hydrazo, Azo and Azoxy CompoundsAllan J. DolenkoEastern Forest Products Laboratory, Canadian Forestry Service Environment Canada, Ottawa, Ontario,Canada K1A OW5
Erwin BuncelDepartment of Chemistry, Queen’s University, Kingston, Ontario, Canada K7L 3N6
Chapter 18. Rearrangements of Hydrazo, Azoxy and Azo CompoundsRobin A. CoxDepartment of Chemistry, Queen’s University, Kingston, Ontario, Canada, K7L 3N6
Erwin BuncelDepartment of Chemistry, Queen’s University, Kingston, Ontario, Canada, K7L 3N6
Chapter 19. Radical Reactions of Azo, Hydrazo and Azoxy CompoundsGen KogaIbaraki University, Mito, Japan
Nobuko KogaIbaraki University, Mito, Japan
29
J.-P. AnselmeUniversity of Massachusetts at Boston, Boston, Massachusetts 02125, U.S.A.
Chapter 20. The Photochemistry of the Hydrazo, Azo and Azoxy GroupsRobert J. DrewerSciences Department, Avondale College, Cooranbong, N.S.W. 2265 Australia
Chapter 21. Conformational Analysis of HydrazinesYouval ShvoDepartment of Chemistry, Tel-Aviv University, Tel-Aviv, Israel
The Chemistry of Cyanates and Their Thio Derivatives, Part 1 (1977)Edited by Saul Patai
Chapter 1. Electronic structure of the cyanato and thiocyanato groups—ground state and excitedstatesKlaus WittelThe Coates Chemical Laboratories, The Louisiana State University, Baton Rouge, Louisiana 70803, U.S.A.
James L. MeeksThe Coates Chemical Laboratories, The Louisiana State University, Baton Rouge, Louisiana 70803, U.S.A.
Seen P. McGlynnThe Coates Chemical Laboratories, The Louisiana State University, Baton Rouge, Louisiana 70803, U.S.A.
Chapter 2. Structural chemistry of the cyanates and their thio derivativesIstvan HargittaiCentral Research Institute of Chemistry of the Hungarian Academy of Sciences, H-1088 Budapest, Puskinutca 11–13, Hungary
Iain C. PaulDepartment of Chemistry, School of Chemical Sciences. University of Illinois, Urbana, Illinois,61801, U.S.A.
Chapter 3. Stereochemical and conformational aspects of cyanates and related groupsGeorge C. CorfieldSheffield City Polytechnic, England
Chapter 4. The optical rotatory dispersion and circular dichroism of the cyanates and relatedgroupsC. TonioloUniversity of Padova, Padova, Italy
Chapter 5. Detection and determination of cyanates, isocyanates, isothiocyanates, and thiocyanatesBen- David A. EfraimThe Weizmann Institute of Science, Rehovot, Israel
Chapter 6. Thermochemistry of cyanates, isocyanates, and their thio derivativesRobert ShawPhysical Sciences Division, Stanford Research Institute, Menlo Park. California 94025, U.S.A.
Chapter 7. Mass spectra of cyanates, isocyanates, and related compoundsK. A. JensenUniversity of Copenhagen, Denmark
30
Gustav SchrollUniversity of Copenhagen, Denmark
Chapter 8. Hydrogen bonding and complex formationDusan HadziUniversity of Ljubljana, Ljubljana, Yugoslavia
Svetozar MilicevUniversity of Ljubljana, Ljubljana, Yugoslavia
Chapter 9. The electrochemistry of cyanates and related compoundsOle HammerichDepartment of General and Organic Chemistry, The H. C. Ørsted Institute, University of Copenhagen,Universitetsparken 5. DK-2100 Copenhagen, Denmark
Vernon D. ParkerDepartment of General and Organic Chemistry, The H. C. Ørsted Institute, University of Copenhagen,Universitetsparken 5. DK-2100 Copenhagen, Denmark
Chapter 10. Photochemistry of cyanates and related groupsR. JahnUniversity of Vienna, Austria
U. SchmidtUniversity of Vienna, Austria
Chapter 11. Radiation chemistry of organic compounds containing OCN, CNO, SCN,and CNS groupsAbraham HorowitzSoreq Nuclear Research Centre, Yavne, Israel
Chapter 12. Kinetics and mechanisms of reactions of cyanates and related compoundsDion E. GilesSchool of Mathematical and Physical Sciences, Murdoch University, Murdoch, Western Australia
Chapter 13. Acyl and thioacyl derivatives of isocyanates, thiocyanates and isothiocyanatesOtohiko TsugeResearch Institute of Industrial Science, Kyushu University, Fukuoka, Japan
Chapter 14. Syntheses and uses of isotopically labelled cyanates and related groupsAlberto CecconIstituto di Chimica Fisica and Istituto di Chimica Organica, Universita’ di Padova, Padova, Italy
Umberto MiottiIstituto di Chimica Fisica and Istituto di Chimica Organica, Universita’ di Padova, Padova, Italy
Chapter 15. Pyrolytic reactions of cyanates and related compoundsNestor BarroetaPetroleum and Chemistry Centre, Instituto Venezolano de Investigaciones Cientıficas, Apartado 1827,Caracas, Venezuela
Chapter 16. Syntheses and preparative applications of cyanates (esters of cyanic acid)K. A. JensenUniversity of Copenhagen, Denmark
Arne HolmUniversity of Copenhagen, Denmark
31
Chapter 17. Syntheses and preparative applications of isocyanatesReinhard RichterThe Upjohn Company, Donald S. Gilmore Research Laboratories, North Haven, Connecticut 06473, U.S.A.
Henri UlrichThe Upjohn Company, Donald S. Gilmore Research Laboratories, North Haven, Connecticut 06473, U.S.A.
Chapter 18. Syntheses and preparative applications of thiocyanatesR. G. GuySchool of Natural Sciences, The Hatfield Polytechnic. Hatfield, Hertfordshire, England
Chapter 19. Selenocyanates and related compoundsE. BulkaErnst-Moritz-Arndt Universitat, Greifswald, D.D.R.
Chapter 20. Biological formation and reactions of cyanatesSasson CohenDepartment of Physiology and Pharmacology, Sackler School of Medicine, Tel-Aviv University, Israel
Edna OppenheimerDepartment of Physiology and Pharmacology, Sackler School of Medicine, Tel-Aviv University, Israel
Chapter 21. Syntheses and reactions of isocyanide dilhalidesHenri UlrichThe Upjohn Company, Donald S. Gilmore Research Laboratories, North Haven, Connecticut 06473, U.S.A.
Reinhard RichterThe Upjohn Company, Donald S. Gilmore Research Laboratories, North Haven, Connecticut 06473, U.S.A.
Chapter 22. The chemistry of the —NCS groupL. DrobnicaSlovak Polytechnical University, Bratislava, Czechoslovakia
P. KristianP. J. Safarik University, Kosice, Czechoslovakia
J. AugustınSlovak Polytechnical University, Bratislara, Czechoslovakia
The Chemistry of Double-Bonded Functional Groups, Volume 1, Part 1 (1977)(See Volume 2 in 1989)
Edited by Saul Patai
Chapter 1. Dipole moments, configurations and conformations of molecules containing X=Y groupsOtto ExnerInstitute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, Prague,Czechoslovakia
Chapter 2. Liquid crystals with X=Y groupsJ. P. Van MeterEastman Kodak Company, Rochester, New York, U.S.A.
Chapter 3. Thermochemistry of X=Y groupsRobert ShawPhysical Sciences Division, Stanford Research Institute, Menlo Park, California 94025, U.S.A.
32
Chapter 4. Mechanisms of elimination and addition reactions involving the X=Y groupAnthony F. CockerillLilly Research Centre Limited, Erl Wood Manor, Windlesham, Surrey, U.K.
Roger G. HarrisonLilly Research Centre Limited, Erl Wood Manor, Windlesham, Surrey, U.K.
Chapter 5. The electrochemistry of X=Y groupsAlbert J. FryWesleyan University, Middletown, Connecticut, U.S.A.
Roberta Gable ReedThe Mary Imogene Bassett Hospital, Cooperstown, New York, U.S.A.
Chapter 6. 1,3-Dipolar cycloadditions involving X=Y groupsGiorgio BianchiInstitute of Organic Chemistry, University of Pavia, Italy
Carlo De MicheliInstitute of Organic Chemistry, University of Pavia, Italy
Remo GandolfiInstitute of Organic Chemistry, University of Pavia, Italy
Chapter 7. Reactions of carbenes with X=Y groupsAlan P. MarchandDepartment of Chemistry, University of Oklahoma, Norman, Oklahoma 73069, U.S.A.
Chapter 8. The formation of unsaturated groups by heterolytic fragmentationKonrad B. BeckerInstitute of Organic Chemistry, University of Basel, Switzerland
Cyril A. GrobInstitute of Organic Chemistry, University of Basel, Switzerland
Chapter 9. Electrophilic additions to carbon–carbon double bondsGeorge H. SchmidDepartment of Chemistry, University of Toronto, Toronto, Ontario, Canada
Dennis G. GarrattDepartment of Chemistry, University of Toronto, Toronto, Ontario, Canada
Chapter 10. The olefin metathesis reactionNissim CalderonThe Goodyear Tire & Rubber Co., Akron, Ohio, U.S.A.
Chapter 11. Oxidation of C=C and C=N groupsP. M. HenryDepartment of Chemistry, University of Guelph, Guelph, Ontario, Canada
G. L. LangeDepartment of Chemistry, University of Guelph, Guelph, Ontario, Canada
Chapter 12. Transition metal catalysed carbonylation of olefinsJohn K. StilleUniversity of Iowa, Iowa City, Iowa, U.S.A.
33
David E. JamesUniversity of Iowa, Iowa City, Iowa, U.S.A.
Chapter 13. Imidines and diamidides (1,3,5-triazapentadienes)John A. ElvidgeChemistry Department, University of Surrey, England
N. R. BarotChemistry Department, University of Nairobi, Kenya
The Chemistry of the Carbon–Carbon Triple Bond, Part 1 (1978)Edited by Saul Patai
Chapter 1. General and theoretical aspects of the acetylenic compoundsM. SimonettaIstituto di Chimica Fisica e Centro CNR, Universita di Milano, Milan, Italy
A. GavezzottiIstituto di Chimica Fisica e Centro CNR, Universita di Milano, Milan, Italy
Chapter 2. The structural chemistry of the C≡C bondJ. L. HencherUniversity of Windsor, Windsor, Ontario, Canada
Chapter 3. Thermochemistry of acetylenesRobert Shaw1162 Quince Avenue, Sunnyvale, California 94087, U.S.A.
Chapter 4. Acidity, hydrogen bonding and complex formationA. C HopkinsonYork University, Downsview, Ontario, Canada
Chapter 5. Detection and determination of alkynesK. A. ConnorsSchool of Pharmacy, University of Wisconsin, Madison, Wisconsin, U.S.A.
Chapter 6. Mass spectrometry of acetylenesC. LifshitzThe Hebrew University, Jerusalem, Israel
A. MandelbaumTechnion-Israel Institute of Technology, Haifa, Israel
Chapter 7. Applications of acetylenes in organic synthesisPaul F. HudrlikRutgers University, New Brunswick, New Jersey, U.S.A.
Anne M. HudrlikRutgers University, New Brunswick, New Jersey, U.S.A.
Chapter 8. Electrophilic additions to carbon–carbon triple bondsGeorge H. SchmidUniversity of Toronto, Toronto, Ontario, Canada
34
Chapter 9. Propargylic metalationJ. KleinThe Hebrew University, Jerusalem, Israel
Chapter 10. Rearrangements involving acetylenesF. TheronUniversite de Clermont-Ferrand, France
M. VernyUniversite de Clermont-Ferrand, France
R. VessiereUniversite de Clermont-Ferrand, France
Chapter 11. Cycloadditions and cyclizations involving triple bondsJ. BastideCentre Universitaire, Perpignan, France
O. Henri-RousseauCentre Universitaire, Perpignan, France
Chapter 12. Photochemistry of the C≡C bondJ. D. CoyleThe Polytechnic, Wolverhampton, England
Chapter 13. Synthetic acyclic polyacetylenesW. D. HuntsmanOhio University, Athens, Ohio
Chapter 14. Natural acetylenesEwart R. H. JonesThe Dyson Perrins Laboratory, Oxford University, Oxford, England
Viktor ThallerThe Dyson Perrins Laboratory, Oxford University, Oxford, England
Chapter 15. Cyclic acetylenesM. NakagawaOsaka University, Toyonaka, Osaka 560, Japan
Chapter 16. Proximity interactions of acetylenesS. MisumiISIR, Osaka University, Suita, Osaka, Japan
T. KanedaISIR, Osaka University, Suita, Osaka, Japan
Chapter 17. The electrochemistry of the carbon–carbon triple bondJ. H. P. UtleyQueen Mary College, London, England
R. LinesChemical Centre, University of Lund, Lund, Sweden
Chapter 18. The preparation of acetylenes and their protectionDavid A. Ben-EfraimThe Weizmann Institute of Science, Rehovot, Israel
35
Chapter 19. Nucleophalic attacks on acetylenesJ. I. DicksteinCollege of Du Page, Glen Ellyn, Illinois, U.S.A.
S. I. MillerIllinois Institute of Technology, Chicago, Illinois, U.S.A.
Chapter 20. Synthesis and uses of isotopically labelled acetylenesJ. C. LavalleyU.E.R. de Sciences, Universite de Caen, 14032 Caen Cedex, France
J. SausseyU.E.R. de Sciences, Universite de Caen, 14032 Caen Cedex, France
The Chemistry of Diazonium and Diazo Groups, Part 1 (1978)Edited by Saul Patai
Chapter 1. General and theoretical aspects of the diazonium and diazo groupsJ. B. MoffatDepartment of Chemistry, University of Waterloo, Waterloo, Ontario, Canada
Chapter 2. Diazonium-diazo equilibriumVojeslav SterbaOrganic Chemistry Department, Institute of Chemical Technology, 532 10 Pardubice, Czechoslovakia
Chapter 3. Structural chemistryS. SorrisoIstituto di Chimica Fisica, Universita di Perngia, 06100 Perugia, Italy
Chapter 4. Thermochemistry of diazo compounds and organic azidesRobert Shaw1162 Quince Avenue, Sunnyvale, California 94087, USA
Chapter 5. Detection and determination of diazo and diazonium groupsDavid A. Ben-EfraimThe Weizmann Institute of Science, Rehovot, Israel
Chapter 6. Basicity, acidity and hydrogen bondingJ. F. McGarrityInstitute of Organic Chemistry, University of Lausanne, Lausanne, Switzerland
Chapter 7. Complex formationHermann M. NiemeyerInstitute of Organic Chemistry, University of Lausanne, Lausanne, Switzerland
Chapter 8. Synthetic applications of diazonium ionsD. S. WulfmanDepartment of Chemistry, University of Missouri-Rolla, Rolla, Mo 65401, USA Equipe de RechercheNo. 12 du CNRS, Laboratoire de Chimie, Ecole Normale Superieure, Paris, France
Chapter 9. Photochemistry of the diazonium and diazo groupsWataru AndoChemistry Department, The University of Tsukuba, Niiharigun, Ibaraki 300-31, Japan
36
Chapter 10. The electrochemistry of the diazo and diazonium groupsAlbert J. FryWesleyan University, Middletown, Connecticut, USA
Chapter 11. The influence of the diazo and diazonium groupsEdward S. LewisDepartment of Chemistry, Rice University, Houston, Texas, USA
Chapter 12. Kinetics and mechanisms of reactions involving diazonium and diazo groupsA. F. HegartyChemistry Department, University College, Cork, Ireland
Chapter 13. Rearrangements involving the diazo and diazonium groupsD. WhittakerDepartment of Organic Chemistry, University of Liverpool, England
Chapter 14. Preparation of diazonium groupsK. SchankFachbereich 14.1 Organische Chemie, Universitat des Saarlandes, D-6600 Saarbrucken, Germany
Chapter 15. Synthesis of diazoalkanesM. RegitzDepartment of Chemistry, University of Kaiserslautern, D-6750 Kaiserslautern, Federal Republic ofGermany
Chapter 16. Preparation and uses of isotopically labelled diazonium and diazo compoundsPeter J. SmithDepartment of Chemistry and Chemical Engineering, University of Saskatchewan, Saskatoon,Saskatchewan, Canada
Kenneth C. WestawayDepartment of Chemistry, Laurentian University, Sudbury, Ontario, Canada
Chapter 17. Carbonyl, phosphoryl and sulphonyl diazo compoundsM. RegitzDepartment of Chemistry, University of Kaiserslautern, D-6750 Kaiserslautern, Federal Republic ofGermany
Chapter 18. Synthetic applications of diazoalkanes, diazocyclopentadienes anddiazoazacyclopentadienesD. S. WulfmanDepartment of Chemistry, University of Missouri-Rolla, Rolla, Mo. 65401, USA Equipe de RechercheNo. 12 du CNRS, Laboratoire de Chimie, Ecole Normale Superieure, Paris, France
G. LinstrumelleEquipe de Recherche No. 12 du CNRS, Laboratoire de Chimie, Ecole Normale Superieure, Paris, France
C. F. CooperDepartment of Chemistry, University of Missouri-Rolla, Rolla, Mo. 65401, USA
37
The Chemistry of Acid Derivatives, Volume 1, Part 1 (1979) (See Volume 2 in 1992)
Edited by Saul Patai
Chapter 1. Recent advances in the theoretical treatment of acid derivativesI. G. CsizmadiaDepartment of Chemistry, University of Toronto, Toronto, Ontario, Canada
M. R. PetersonDepartment of Chemistry, University of Toronto, Toronto, Ontario, Canada
C. KozmutzaPhysical Institute, Technical University, Budapest, Hungary
M. A. RobbDepartment of Chemistry. Queen Elizabeth College, University of London, London, England
Chapter 2. Thermochemistry of acid derivativesRobert Shaw1162 Quince Avenue, Sunnyvale. California. 94087, U.S.A.
Chapter 3. Chiroptical properties of acid derivativesRolf HakanssonDivision of Organic Chemistry 1, Chemical Centre, University of Lund, Sweden
Chapter 4. Mass spectra of acid derivativesS. W. TamDepartment of Chemistry, Chung Chi College, The Chinese University of Hong Kong, Shatin, N. T.,Hong Kong
Chapter 5. Complexes of acid anhydridesR. FosterChemistry Department, University of Dundee, Dundee, Scotland
Chapter 6. Hydrogen bonding in carboxylic acids and derivativesDusan HadziUniversity of Ljubljana, Yugoslavia
Snegulka DetoniUniversity of Ljubljana, Yugoslavia
Chapter 7. The synthesis of carboxylic acids and esters and their derivativesMichael A. OgliarusoDepartment of Chemistry, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, U.S.A.
James F. WolfeDepartment of Chemistry, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, U.S.A.
Chapter 8. The chemistry of lactones and lactamsG. V. BoydDepartment of Chemistry, Chelsea College, London
Chapter 9. The chemistry of orthoamides of carboxylic acids and carbonic acidW. KantlehnerFachhochschule Aalen, Aalen, Germany
38
Chapter 10. Detection and determination of acid derivativesW. H. PrichardThe City University, London, England
Chapter 11. The photochemistry of organic acids, esters, anhydrides, lactones and imidesRichard S. GivensChemistry Department, The University of Kansas, Lawrence, Kansas 66045, U.S.A.
Nissim LeviChemistry Department, The University of Kansas, Lawrence, Kansas 66045, U.S.A.
Chapter 12. Radiation chemistry of acids, esters, anhydrides, lactones and lactamsO. I. MicicBoris Kidric Institute of Nuclear Sciences, Vinca-Belgrade, Yugoslavia
O. S. GalBoris Kidric Institute of Nuclear Sciences, Vinca-Belgrade, Yugoslavia
Chapter 13. The electrochemistry of carboxylic acids and derivatives: Cathodic reductionsJames P. ColemanCorporate Research Department, Monsanto Company, St. Louis, Missouri 63166, U.S.A.
Chapter 14. Decarbonylation reactions of acid halides and aldehydes bychlorotris-(triphenylphosphine)rhodium(i)M. C. BairdDepartment of Chemistry, Queen’s University, Kingston, Canada
Chapter 15. Pyrolysis of acids and their derivativesR. TaylorUniversity of Sussex, Faimer, Brighton, U.K.
Chapter 16. Transcarboxylation reactions of salts of aromatic carboxylic acidsJosef RatuskyInstitute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, Prague,Czechoslovakia
Chapter 17. Micellar effects upon deacylationC. A. BuntonDepartment of Chemistry, University of California, Santa Barbara, Ca. 93106, U.S.A.
L. S. RomstedDepartment of Chemistry, University of California, Santa Barbara, Ca. 93106, U.S.A.
Chapter 18. The chemistry of thio acid derivativesJ. VossInstitute for Organic Chemistry and Biochemistry, University of Hamburg, Hamburg, Germany
Chapter 19. The synthesis of lactones and lactamsJames F. WolfeVirginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, U.S.A.
Michael A. OgliarusoVirginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, U.S.A.
39
The Chemistry of Ketenes, Allenes and Related Compounds, Part 1 (1980)Edited by Saul Patai
Chapter 1. Theoretical methods and their application to ketenes and allenesClifford E. DykstraSchool of Chemical Sciences, University of Illinois, Urbana, Illinois 61801, U.S.A.
Henry F. Schaefer IIIDepartment of Chemistry, University of California, Berkeley, California 94720, U.S.A.
Chapter 2. Structural chemistryWolfgang RungeOrganisch-Chemisches Institut der Technischen Universitat Munchen, Germany
Chapter 3. Chirality and chiroptical propertiesWolfgang RungeOrganisch-Chemisches Institut der Technischen Universitat Munchen, Germany
Chapter 4. The thermodynamics of allenes, ketenes and related compoundsRichard L. DemingDepartment of Chemistry, California State University at Fullerton, Fullerton, U.S.A.
Claus A. WulffDepartment of Chemistry, University of Vermont, Burlington, U.S.A.
Chapter 5. Detection, determination and identification of allenes and ketenesJames W. MunsonCollege of Pharmacy, University of Kentucky, Lexington, Kentucky 40506, U.S.A.
Chapter 6. The generation of neutral and ionized allenes, cumulenes and heterocumulenes byelectron impactHelmut SchwarzInstitut fur Organische Chemie, Technische Universitat Berlin, Berlin, West Germany
Claus KoppelInstitut fur Organische Chemie, Technische Universitat Berlin, Berlin, West Germany
Chapter 7. The preparation of ketenesR. S. WardDepartment of Chemistry, University College of Swansea, Swansea, U.K.
Chapter 8. Synthetic uses of ketenes and allenesWilliam T. BradyDepartment of Chemistry, North Texas State University, Denton, Texas 76203, U.S.A.
Chapter 9. Kinetics and mechanisms (excepting cycloadditions)Peter BlakeUniversity College, Cardiff, U.K.
Chapter 10. Organometallic derivatives of allenes and ketenesJean-Louis MoreauUniversite Pierre et Marie Curie, Paris, France
40
Chapter 11. Preparation and uses of isotopically labelled allenesM. D. SchiavelliDepartment of Chemistry, The College of William and Mary in Virginia, Williamsburg, Virginia, U.S.A.
Chapter 12. Electrochemistry of allenes and cumulenesDennis G. PetersDepartment of Chemistry, Indiana University, Bloomington, Indiana 47405, U.S.A.
William F. Carroll Jr.Department of Chemistry, Indiana University, Bloomington, Indiana 47405, U.S.A.
Daniel M. La PerriereDepartment of Chemistry, Indiana University, Bloomington, Indiana 47405, U.S.A.
Brian C. WillettDepartment of Chemistry, Indiana University, Bloomington, Indiana 47405, U.S.A.
Chapter 13. Biological formation and reactionsCecil H. RobinsonThe Johns Hopkins University, School of Medicine, Baltimore, Maryland, U.S.A.
Douglas F. CoveyWashington University, School of Medicine, St. Louis, Missouri, U.S.A.
Chapter 14. Ketene O,O-acetalsPaul BrassardDepartement de Chimie, Universite Laval, Quebec, Canada
Chapter 15. Rearrangements involving allenesWilliam D. HuntsmanOhio University, Athens, Ohio, U.S.A.
Chapter 16. Ketene thioacetalsM. KolbMerrell International Research Centre, Strasbourg, France
Chapter 17. Ketene iminesMarvin W. BarkerDepartment of Chemistry, Mississippi State University, Mississippi State, Mississippi, U.S.A.
William E. McHenryDepartment of Chemistry, Mississippi State University, Mississippi State, Mississippi, U.S.A.
Chapter 18. CarbodiimidesYecheskel WolmanDepartment of Organic Chemistry, The Hebrew University, Jerusalem, Israel
Chapter 19. MethyleneketenesRoger F. C. BrownMonash University, Clayton, Victoria, Australia
Frank W. EastwoodMonash University, Clayton, Victoria, Australia
Chapter 20. The preparation of allenes and cumulenesHenning HopfUniversity of Wurzburg, Am Hubland, D-8700 Wurzburg, Germany
41
The Chemistry of Ethers, Crown Ethers, Hydroxyl Groups and their Sulphur Analogues,Part 1 (1981)Edited by Saul Patai
Chapter 1. Synthesis of crown ethers and analoguesDale A. LaidlerI.C.I. Corporate Laboratory, Runcorn, England and University of Sheffield, England
J. Fraser StoddartI.C.I. Corporate Laboratory, Runcorn, England and University of Sheffield, England
Chapter 2. Crown ethers–complexes and selectivityFritz VogtleInstitut fur Organische Chemie und Biochemie der Universitat, Gerhard-Domagk Strasse 1, D-5300 Bonn,West Germany
Edwin WeberInstitut fur Organische Chemie und Biochemie der Universitat, Gerhard-Domagk Strasse 1, D-5300 Bonn,West Germany
Chapter 3. Organic transformations mediated by macrocyclic multidentate ligandsCharles L. LiottaSchool of Chemistry, Georgia Institute of Technology, Atlanta, Georgia 30332, U.S.A.
Chapter 4. Geometry of the ether, sulphide and hydroxyl groups and structural chemistry ofmacrocyclic and non-cyclic polyether compoundsIsrael GoldbergInstitute of Chemistry, Tel-Aviv University, 61390 Tel-Aviv, Israel
Chapter 5. Stereodynamics of alcohols, ethers, thio ethers and related compoundsC. Hackett BushwellerDepartment of Chemistry, University of Vermont, Burlington, Vermont 05405, U.S.A.
Michael H. GianniDepartment of Chemistry, St. Michael’s College, Winooski, Vermont 05404, U.S.A.
Chapter 6. Chiroptical properties of alcohols, ethers, thio ethers and disulphidesG. GottarelliFaculty of Industrial Chemistry, University of Bologna, Italy
B. SamoriFaculty of Industrial Chemistry, University of Bologna, Italy
Chapter 7. The mass spectra of ethers and sulphidesChristian C. Van De SandeDepartment of Organic Chemistry, State University of Gent, Krijgslaan, 271 (Block S.4), B-9000Gent, Belgium
Chapter 8. The electrochemistry of ethers, hydroxyl groups and their sulphur analoguesTatsuya ShonoDepartment of Synthetic Chemistry, Kyoto University, Kyoto 606, Japan
42
Chapter 9. Electronic structures and thermochemistry of phenolsJean RoyerGroupe de Physique Moleculaire et Chimie Organique Quantiques, C.N.R.S. of France (E.R.A. 600),Universite Claude Bernard Lyon I, 43, Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cedex,France
Guy BertholonGroupe de Recherches sur les Phenols, C.N.R.S. of France (E.R.A. 600), Universite Claude Bernard LyonI, 43, Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cedex, France
Robert PerrinGroupe de Recherches sur les Phenols, C.N.R.S. of France (E.R.A. 600), Universite Claude Bernard LyonI, 43, Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cedex, France
Roger LamartineGroupe de Recherches sur les Phenols, C.N.R.S. of France (E.R.A. 600), Universite Claude Bernard LyonI, 43, Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cedex, France
Monique PerrinLaboratoire de Mineralogie-Cristallographie, C.N.R.S. of France (E.R.A. 600), Universite Claude BernardLyon I, 43, Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cedex, France
Chapter 10. Syntheses and uses of isotopically labelled ethers and sulphidesMieczyslaw ZielinskiInstitute of Chemistry, Jagiellonian University, Cracow, Poland
Chapter 11. Gas-phase thermal decompositions of simple alcohols, thiols and sulphidesR. L. FailesMacquarie University, New South Wales 2113, Australia
J. S. ShapiroMacquarie University, New South Wales 2113, Australia
V. R. StimsonUniversity of New England, Armidale 2351, Australia
Chapter 12. Oxidation and reduction of alcohols and ethersPaul MullerDepartement de Chimie Organique, Universite de Geneve, Geneve, Suisse
Chapter 13. Oxidation and reduction of sulphidesEric BlockDepartment of Chemistry, University of Missouri-St. Louis, St. Louis, Missouri 63121, U.S.A.
Chapter 14. OxiranesM. BartokDepartment of Organic Chemistry, Jozsef Attila University, Szeged, Hungary
K. L. LangDepartment of Organic Chemistry, Jozsef Attila University, Szeged, Hungary
Chapter 15. Cyclic ethersM. BartokDepartment of Organic Chemistry, Jozsef Attila University, Szeged, Hungary
Chapter 16. Dehydration of diolsM. BartokDepartment of Organic Chemistry, Jozsef Attila University, Szeged, Hungary
43
A. MolnarDepartment of Organic Chemistry, Jozsef Attila University, Szeged, Hungary
Chapter 17. Enol ethers—structure, synthesis and reactionsPeter FischerInstitut fur Organische Chemie, Biochemie und Isotopenforschung, Universitat Stuttgart, Stuttgart,Bundesrepublik Deutschland
Chapter 18. Oxathiacyclanes: preparation, structure and reactionsK. PihlajaDepartment of Chemistry, University of Turku, SF-20500 Turku 50, Finland
P. PasanenDepartment of Chemistry, University of Turku, SF-20500 Turku 50, Finland
Chapter 19. Allene oxides and related speciesPeter J. StangChemistry Department, The University of Utah, Salt Lake City, Utah 84112, U.S.A.
Chapter 20. Advances in the chemistry of acetals, ketals and ortho estersR. G. BergstromCalifornia State University, Hayward, California, U.S.A.
Chapter 21. The photochemistry of saturated alcohols, ethers and acetalsClemens Von SonntagInstitut fur Strahlenchemie im Max-Planck-Institut fur Kohlenforschung, Stiftstrasse 34–36, D-4330Mulheim a. d. Ruhr, W. Germany
Heinz-Peter SchuchmannInstitut fur Strahlenchemie im Max-Planck-Institut fur Kohlenforschung, Stiftstrasse 34–36, D-4330Mulheim a. d. Ruhr, W. Germany
Chapter 22. The photolysis of saturated thiols, sulphides and disulphidesClemens Von SonntagInstitut fur Strahlenchemie im Max-Planck-Institut fur Kohlenforschung, Stiftstrasse 34–36, D-4330Mulheim a. d. Ruhr, W. Germany
Heinz-Peter SchuchmannInstitut fur Strahlenchemie im Max-Planck-Institut fur Kohlenforschung, Stiftstrasse 34–36, D-4330Mulheim a. d. Ruhr, W. Germany
Chapter 23. Radiation chemistry of alcohols and ethersClemens Von SonntagInstitut fur Strahlenchemie im Max-Planck-Institut fur Kohlenforschung, Stiftstrasse 34–36, D-4330Mulheim a. d. Ruhr, W. Germany
Heinz-Peter SchuchmannInstitut fur Strahlenchemie im Max-Planck-Institut fur Kohlenforschung, Stiftstrasse 34–36, D-4330Mulheim a. d. Ruhr, W. Germany
Chapter 24. Radiation chemistry of thiols, sulphides and disulphidesClemens Von SonntagInstitut fur Strahlenchemie im Max-Planck-Institut fur Kohlenforschung, Stiftstrasse 34–36, D-4330Mulheim a. d. Ruhr, W. Germany
44
Heinz-Peter SchuchmannInstitut fur Strahlenchemie im Max-Planck-Institut fur Kohlenforschung, Stiftstrasse 34–36, D-4330Mulheim a. d. Ruhr, W. Germany
The Chemistry of the Sulphonium Group, Part 1 (1981)Edited by Charles J. M. Stirling
Chapter 1. General and theoretical aspectsM. SimonettaIstituto di Chimica Fisica e Centro CNR, Universita di Milano, Milan, Italy
A. GavezzottiIstituto di Chimica Fisica e Centro CNR, Universita di Milano, Milan, Italy
Chapter 2. The structural chemistry of sulphonium saltsEdmund F. PerozziEthyl Corporation, 1600 West Eight Mile Road, Ferndale, Michigan 48220, USA
Iain C. PaulDepartment of Chemistry, School of Chemical Sciences, University of Illinois, Urbana, Illinois 61801, USA
Chapter 3. Analysis and determinationM. R. F. AshworthLehrstuhl fur Organische Analytik, Universitat des Saarlandes, Saarbrucken, W. Germany
Chapter 4. Thermochemistry of the sulphonium groupRobert ShawChemistry Department, Lockheed Palo Alto Research Laboratory, Lockheed Missiles & Space Company,Inc., 3251 Hanover Street, Palo Alto, California 94304, USA
Chapter 5. Photochemistry of sulphonium compoundsJ. D. CoyleChemistry Department, The Open University, Milton Keynes MK7 6AA, England
Chapter 6. Electronic spectraG. C. BarrettOxford Polytechnic, Headington, Oxford OX3 OBP, England
Chapter 7. Electrochemistry of the sulphonium groupJ. GrimshawDepartment of Chemistry, David Keir Building, Queen’s University of Belfast, Belfast BT9 5AG, N. Ireland
Chapter 8. Isofopically labelled sulphonium saltsLeonard F. BlackwellDepartment of Chemistry, Biochemistry and Biophysics, Massey University, Palmerston North,New Zealand
Chapter 9. Electronic effects of the sulphonium groupJohn ShorterDepartment of Chemistry, The University, Hull HU6 7RX, England
45
Chapter 10. Stereochemistry and chiroptical properties of the sulphonium groupK. K. AndersenDepartment of Chemistry, University of New Hampshire, Durham, New Hampshire 03824, USA
Chapter 11. Synthesis of sulphonium saltsP. A. LoweThe Ramage Laboratories, Department of Chemistry and Applied Chemistry, University of Salford, SalfordM5 4WT, England
Chapter 12. Reactivity of sulphonium saltsA. C. KnipeSchool of Physical Sciences, The New University of Ulster, Coleraine, Co. Londonderry, N. Ireland BT421SA
Chapter 13. Cyclic sulphonium saltsDonald C. DittmerDepartment of Chemistry, Syracuse University, Syracuse, N.Y. 13210, USA
Bhalchandra H. PatwardhanDepartment of Chemistry, Syracuse University, Syracuse, N.Y. 13210, USA
Chapter 14. Qrganosulphur cation radicalsHenry J. ShineDepartment of Chemistry, Texas Tech University, Lubbock, Texas 79409, USA
Chapter 15. Heterosulphonium saltsShigeru OaeDepartment of Chemistry, University of Tsukuba, Sakura-mura, Ibaraki, 305 Japan
Tatsuo NumataDepartment of Chemistry, University of Tsukuba, Sakura-mura, Ibaraki, 305 Japan
Toshiaki YoshimuraDepartment of Chemistry, University of Tsukuba, Sakura-mura, Ibaraki, 305 Japan
Chapter 16. Synthetic applications of sulphonium salts and sulphonium ylidesEric BlockDepartment of Chemistry, University of Missouri-St. Louis, St. Louis, Missouri 63121, USA
Chapter 17. The biochemistry of sulphonium saltsG. A. MawDepartment of Biochemistry, Glasshouse Crops Research Institute, Littlehampton, Sussex, England
The Chemistry of Amino, Nitroso and Nitro Compounds and Their Derivatives,Part 1 (1982)Edited by Saul Patai
Chapter 1. Structural chemistryS. SorrisoDipartimento di Chimica, Universita di Perugia, 06100 Perugia, Italy
Chapter 2. Stereochemistry and conformationsMorton RabanDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202, U.S.A.
46
Jeremy GreenblattDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202, U.S.A.
Chapter 3. The chemistry of ionized amino, nitroso and nitro compounds in the gas phaseHelmut SchwarzInstitut fur Organische Chemie, Technische Universitat Berlin, Berlin, West Germany
Karsten LevsenInstitut fur Physikalische Chemie, Universitat Bonn, Bonn, West Germany
Chapter 4. Rearrangements involving nitroso and nitro compoundsD. L. H. WilliamsChemistry Department, University of Durham, Durham, England
Chapter 5. The spectroscopy, photophysics and photochemistry of saturated aminesArthur M. HalpernDepartment of Chemistry, Northeastern University, Boston, Massachusetts 02115, U.S.A.
Chapter 6. Photochemistry of nitro and nitroso compoundsYuan L. ChowDepartment of Chemistry, Simon Fraser University, Burnaby, B.C., Canada
Chapter 7. Radiation chemistry of amines, nitro and nitroso compoundsClive L. GreenstockMedical Biophysics Branch, Atomic Energy of Canada Limited, Whiteshell Nuclear ResearchEstablishment, Pinawa, Manitoba, Canada
Chapter 8. Electrochemistry of nitro compoundsAlbert J. FryWesleyan University, Middletown, Connecticut, U.S.A.
Chapter 9. Electrochemistry of aminesWayne E. BrittonChemistry Department, The University of Texas at Dallas, Richardson, Texas 75080, U.S.A.
Chapter 10. Radical anion reactions of nitro compoundsNathan KornblumDepartment of Chemistry, Purdue University, West Lafayette, Indiana, U.S.A.
Chapter 11. Direct aminationsTuvia SheradskyDepartment of Organic Chemistry, The Hebrew University, Jerusalem, Israel
Chapter 12. Pyrolysis of nitrites, nitrates, nitro compounds, nitroso compounds and aminesLeslie BattDepartment of Chemistry, University of Aberdeen, Aberdeen AB9 2UE, Scotland
Chapter 13. Nitrones and nitronic acid derivatives: their structure and their roles in synthesisEli BreuerDepartment of Pharmaceutical Chemistry, The School of Pharmacy, The Hebrew University of Jerusalem,Jerusalem, Israel
47
Chapter 14. NitroxidesHans Gunter AurichFachbereich Chemie, Philipps-Universitat Marburg, Marburg, Germany
Chapter 15. Enamines and ynaminesG. PitaccoInstitute of Chemistry, University of Trieste, Italy
E. ValentinInstitute of Chemistry, University of Trieste, Italy
Chapter 16. Nitro-activated carbon acidsEdward S. LewisDepartment of Chemistry, Rice University, Houston, Texas 77001, U.S.A.
Chapter 17. Gas-phase basicity and acidity of aminesD. K. BohmeYork University, Downsview, Ontario, Canada
Chapter 18. Special properties of di- and polyaminesRoger W. AlderSchool of Chemistry, University of Bristol, Bristol BS8 1TS, England
Richard B. SessionsInstitut Le Bel, Universite Louis Pasteur, 1 Rue Blaise Pascal, 67008 Strasbourg, France
Chapter 19. Alkyl nitrate nitrationsHenry FeuerDepartment of Chemistry, Purdue University, West Lafayette, Indiana 47907, U.S.A.
Chapter 20. AminalsLucette DuhamelUniversite de Rouen, Faculte des Sciences et des Techniques, 76130 Mont-Saint-Aignan, France
Chapter 21. Detection and determination of nitro and nitroso compoundsY. TapuhiDepartment of Inorganic and Analytical Chemistry, The Hebrew University, Jerusalem, Israel
Eli GrushkaDepartment of Inorganic and Analytical Chemistry, The Hebrew University, Jerusalem, Israel
Chapter 22. Deaminations (carbon–nitrogen bond cleavages)Ronald J. BaumgartenDepartment of Chemistry, University of Illinois at Chicago Circle, Box 4348 Chicago, Illinois60680, U.S.A.
Veronica A. CurtisDepartment of Chemistry, University of Illinois at Chicago Circle, Box 4348 Chicago, Illinois60680, U.S.A.
Chapter 23. Chiroptical properties of amino, nitroso and nitro compoundsHoward E. SmithDepartment of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, U.S.A.
48
Chapter 24. Thermochemistry of nitro compounds, amines and nitroso compoundsLeslie BattDepartment of Chemistry, University of Aberdeen, Meston Walk, Old Aberdeen, AB9 2UE, Scotland
Gillian N. RobinsonDepartment of Chemistry, University of Aberdeen, Meston Walk, Old Aberdeen, AB9 2UE, Scotland
Chapter 25. Oxidation of aminesDavid H. RosenblattU.S. Army Medical Bioengineering Research and Development Laboratory, Fort Detrick, Frederick,Maryland, U.S.A.
Elizabeth P. BurrowsU.S. Army Medical Bioengineering Research and Development Laboratory, Fort Detrick, Frederick,Maryland, U.S.A.
Chapter 26. N-Nitrosamines and N-nitrosoiminesBrian C. ChallisChemistry Department, Imperial College, London, United Kingdom New England Institute for LifeSciences, Waltham, Massachusetts, U.S.A.
Judith A. ChallisChemistry Department, Imperial College, London, United Kingdom New England Institute for LifeSciences, Waltham, Massachusetts, U.S.A.
Chapter 27. The role of Meisenheimer or s-complexes in nitroarene–base interactionsE. BuncelDepartment of Chemistry, Queen’s University, Kingston, Ontario, K7L 3N6, Canada
Chapter 28. Uses of isotopically labelled amino, quaternary ammonium and nitro compoundsPeter J. SmithDepartment of Chemistry and Chemical Engineering, University of Saskatchewan, Saskatoon,Saskatchewan, Canada
Kenneth C. WestawayDepartment of Chemistry, Laurentian University, Sudbury, Ontario, Canada
The Chemistry of Halides, Pseudo-Halides and Azides, Part 1 (1983)Edited by Saul Patai and Zvi Rappoport
Chapter 1. Molecular mechanics and conformationA. Y. MeyerDepartment of Organic Chemistry, Hebrew University, Jerusalem, Israel
Chapter 2. Diamagnetic behaviour of compounds containing carbon–halogen bondsR. R. GuptaDepartment of Chemistry, University of Rajasthan, Jaipur 302004, India
Chapter 3. The mass spectra of azides and halidesJack M. MillerDepartment of Chemistry, Brock University, St Catharines, Ontario, Canada L2S 3A1
Timothy R. B. JonesDepartment of Chemistry, Brock University, St Catharines, Ontario, Canada L2S 3A1
49
Chapter 4. Nuclear quadrupole resonance of carbon-bonded halogensE. A. C. LuckenPhysical Chemistry Department, 30 Quai E. Ansermet, 1211 Geneva, Switzerland
Chapter 5. 1,2-Dehalogenations and related reactionsEnrico BaciocchiDipartimento di Chimica, Universita di Perugia, Perugia, Italy
Chapter 6. Electrochemical oxidation, reduction and formation of the C−X bond—direct andindirect processesJames Y. BeckerDepartment of Chemistry, Ben-Gurion University of the Negev, Beer Sheva, Israel
Chapter 7. Pyrolysis of aryl azidesL. K. DyallDepartment of Chemistry, University of Newcastle, New South Wales, Australia 2308
Chapter 8. Vinyl, aryl and acyl azidesHarold W. MooreDepartment of Chemistry, University of California, Irvine, California 92717, U.S.A.
Dorothy M. GoldishDepartment of Chemistry, California State University Long Beach, Long Beach, California 90840, U.S.A.
Chapter 9. Recent advances in the radiation chemistry of halocarbonsAbraham HorowitzSoreq Nuclear Research Centre, Yavne, Israel
Chapter 10. Organic chemistry of astatineKlara BereiCentral Research Institute for Physics, Budapest, Hungary
Laszlo VasarosCentral Research Institute for Physics, Budapest, Hungary
Chapter 11. Positive halogen compoundsA. FoucaudDepartement de Physique Cristalline et Chimie Structurale, Universite de Rennes, France
Chapter 12. Aspects of the chemistry of halophenols and halodienonesJudith M. BrittainChemistry Department, University of Auckland, Private Bag, Auckland, New Zealand
Peter B. D. De La MareChemistry Department, University of Auckland, Private Bag, Auckland, New Zealand
Chapter 13. a-Halogenated iminesNorbert De KimpeLaboratory of Organic Chemistry, Faculty of Agricultural Sciences, State University of Gent, Coupure533, B-9000 Gent, Belgium
Roland VerheLaboratory of Organic Chemistry, Faculty of Agricultural Sciences, State University of Gent, Coupure533, B-9000 Gent, Belgium
50
Chapter 14. FluorocarbonsB. E. SmartE. I. du Pont de Nemours and Company, Central Research and Development Department, Wilmington,Delaware 19898, USA
Chapter 15. Xenon halide halogenationsMarko ZupanDepartment of Chemistry and ‘Jozef Stefan’ Institute, ‘E. Kardelj’ University of Ljubljana, Ljubljana,Yugoslavia
Chapter 16. The SRN1 reaction of organic halidesRobert K. NorrisDepartment of Organic Chemistry, The University of Sydney, New South Wales 2006, Australia
Chapter 17. Reactions involving solid organic halidesE. HadjoudisSolid State Chemistry Laboratory, ‘Demokritos’ Nuclear Research Centre, Athens, Greece
Chapter 18. Hypervalent halogen compoundsGerald F. KoserDepartment of Chemistry, The University of Akron, Akron, Ohio 44325, USA
Chapter 19. Synthesis and reactivity of a-halogenated ketonesRoland VerheLaboratory of Organic Chemistry, Faculty of Agricultural Sciences, State University of Gent, Coupure533, B-9000 Gent, Belgium
Norbert De KimpeLaboratory of Organic Chemistry, Faculty of Agricultural Sciences, State University of Gent, Coupure533, B-9000 Gent, Belgium
Chapter 20. Electrophilic assistance to reactions at a C−X bondDennis N. KevillDepartment of Chemistry, Northern Illinois University, DeKalb, Illinois 60115, USA
Chapter 21. Molecular interactions involving organic halidesJean-Max DumasLaboratoire de Physico-Chimie des Dielectriques, Faculte de Sciences Fondamentales et Appliquees,Universite de Poitiers, 86022 Poitiers Cedex, France
Maurice GomelLaboratoire de Physico-Chimie des Dielectriques, Faculte de Sciences Fondamentales et Appliquees,Universite de Poitiers, 86022 Poitiers Cedex, France
Maurice GuerinLaboratoire de Physico-Chimie des Dielectriques, Faculte de Sciences Fondamentales et Appliquees,Universite de Poitiers, 86022 Poitiers Cedex, France
Chapter 22. Formation of carbon–halogen bondsMilos HudlickyVirginia Polytechnic Institute and State University, Blacksburg, Virginia, USA
Tomas HudlickyVirginia Polytechnic Institute and State University, Blacksburg, Virginia, USA
51
Chapter 23. Alkene-forming eliminations involving the carbon-halogen bondEnrico BaciocchiDipartimento di Chimica, Universita di Perugia, Perugia, Italy
Chapter 24. Structural chemistry of the carbon–halogen and carbon–pseudohalogen bondsM. KaftoryDepartment of Chemistry, Technion-Israel Institute of Technology, Haifa, Israel
Chapter 25. Halonium ionsGerald F. KoserDepartment of Chemistry, The University of Akron, Akron, Ohio, USA
Chapter 26. Carbon–carbon bond formation involving organic halides and transition metalcompoundsF. NasoIstituto di Chimica Organica, Universita di Bari, Bari, Italy
G. MarcheseIstituto di Chimica Organica, Universita di Bari, Bari, Italy
Chapter 27. DihalocyclopropanesPeter WeyerstahlTechnische Universitat Berlin, Institut fur Organische Chemie, D-1000 Berlin 12, Federal Republic ofGermany
Chapter 28. Photoelectron spectra of organic halogen compoundsK. WittelInstitute of Inorganic Chemistry, Johann Wolfgang Goethe University, Niederurseler Hang, D-6000Frankfurt (M) 50, West Germany
H. BockInstitute of Inorganic Chemistry, Johann Wolfgang Goethe University, Niederurseler Hang, D-6000Frankfurt (M) 50, West Germany
Chapter 29. Recent advances in the photochemistry of the carbon–halogen bondG. LodderGorlaeus Laboratories, University of Leiden, Leiden, The Netherlands
The Chemistry of the Metal–Carbon Bond, Volume 1 (1983) (See Volume 2 in 1985, Volume 3in 1985, Volume 4 in 1987, Volume 5 in 1989)
Edited by Frank R. Hartley and Saul Patai
Chapter 1. Structure of organometallic compoundsA. D. RedhouseDepartment of Chemistry and Applied Chemistry, University of Salford, Salford M5 4WT, UK
Chapter 2. Thermochemistry of organometallic compoundsG. PilcherDepartment of Chemistry, University of Manchester, Manchester M13 9PL, UK
H. A. SkinnerDepartment of Chemistry, University of Manchester, Manchester M13 9PL, UK
52
Chapter 3. Synthesis of ylide complexesLothar WeberFachbereich Chemie, Universitat Essen, Universitatstrasse 5–7, D-4300 Essen 1, Federal Republic ofGermany
Chapter 4. Synthesis of transition metal–carbene complexesHelmut FischerAnorganisch-Chemisches Institut der Technischen Universitat Munchen, Lichtenbergstrasse 4, D-8046Garching, German Federal Republic
Chapter 5. Syntheses of transition metal–carbyne complexesUlrich SchubertAnorganisch-Chemisches Institut der Technischen Universitat Munchen, Lichtenbergstrasse 4, D-8046Garching, German Federal Republic
Chapter 6. Synthesis of transition metal alkyl and aryl complexesR. J. PuddephattDepartment of Chemistry, University of Western Ontario, London, Ontario, N6A 5B7, Canada
Chapter 7. Synthesis of olefin and acetylene complexes of the transition metalsGlenn S. LewandosDepartment of Chemistry, Central Michigan University, Mount Pleasant, Michigan 48859, U.S.A.
Chapter 8. Synthesis of η3-allyl complexesP. PowellDepartment of Chemistry, Royal Holloway College, Egham Hill, Surrey TW20 0EX, UK
Chapter 9. The synthesis of η4-butadiene and cyclobutadiene complexG. MarrDepartment of Physical Sciences, The Polytechnic, Wolverhampton WY1 1LY, UK
B. W. RockettDepartment of Physical Sciences, The Polytechnic, Wolverhampton WY1 1LY, UK
Chapter 10. Synthesis of complexes of η5-bonded ligandsG. MarrDepartment of Physical Sciences, The Polytechnic, Wolverhampton WV1 1LY, UK
B. W. RockettDepartment of Physical Sciences, The Polytechnic, Wolverhampton WV1 1LY, UK
Chapter 11. Synthesis of complexes of η6-, η7-, and η8-bonded ligandsG. MarrDepartment of Physical Sciences, The Polytechnic, Wolverhampton WV1 1LY, UK
B. W. RockettDepartment of Physical Sciences, The Polytechnic, Wolverhampton WV1 1LY, UK
Chapter 12. Synthesis of organolanthanide and organoactinide complexesWilliam J. EvansDepartment of Chemistry, University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA
Chapter 13. Metal atoms in organometallic synthesisMichael J. McGlincheyDepartment of Chemistry, McMaster University, 1280 Main Street West, Hamilton, Ontario, L8S4M1, Canada
53
Chapter 14. Analysis of organometallic compounds: Determination of elements and functionalgroupsT. R. Crompton‘Beechcroft’, Whittingham Lane, Goosnargh, Preston, Lancashire, UK
Chapter 15. Analysis of organometallic compounds: Titration proceduresT. R. Crompton‘Beechcroft’, Whittingham Lane, Goosnargh, Preston, Lancashire, UK
Chapter 16. Analysis of organometallic compounds: Spectroscopic methodsT. R. Crompton‘Beechcroft’, Whittingham Lane, Goosnargh, Preston, Lancashire, UK
Chapter 17. Analysis of organometallic compounds: Polarographic techniquesT. R. CromptonBeechcroft, Whittingham Lane, Goosnargh, Preston, Lancashire, U.K.
Chapter 18. Analysis of organometallic compounds: Gas chromatographyT. R. Crompton‘Beechcroft’, Whittingham Lane, Goosnargh, Preston, Lancashire, UK
Chapter 19. Analysis of organometallic compounds: Other chromatographic techniquesT. R. Crompton‘Beechcroft’, Whittingham Lane, Goosnargh, Preston, Lancashire, UK
Chapter 20. Infrared and Raman spectroscopy of organometallic compoundsMichael J. TaylorDepartment of Chemistry, University of Auckland, Auckland 1, New Zealand
Chapter 21. Multinuclear magnetic resonance methods in the study of organometallic compoundsJulian A. DaviesCollege of Arts and Sciences, Department of Chemistry, The University of Toledo, Toledo, Ohio43606, USA
Chapter 22. Mass spectrometry of organometallic compoundsT. R. SpaldingDepartment of Chemistry, University College, Cork, Ireland
The Chemistry of Peroxides, Volume 1 (1983) (See Volume 2 in 2006)
Edited by Saul Patai
Chapter 1. General and theoretical aspects of the peroxide groupDieter CremerLehrstuhl fur Theoretische Chemie, Universitat Koln, Koln, West Germany
Chapter 2. Stereochemical and conformational aspects of peroxy compoundsOtto ExnerInstitute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 16610 Prague 6,Czechoslovakia
54
Chapter 3. Thermochemistry of peroxidesAlan C. BaldwinDepartment of Chemical Kinetics, SRI International, Menlo Park, California 94025, U.S.A.
Chapter 4. Mass spectrometry of organic peroxidesHelmut SchwarzInstitut fur Organische Chemie, Technische Universitat Berlin, D-1000 Berlin 12, W. Germany
Hans-Martin SchiebelInstitut fur Organische Chemie, Technische Universitat Braunschweig, D-3300 Braunschweig, W. Germany
Chapter 5. Acidity, hydrogen bonding and complex formationWilliam H. RichardsonSan Diego State University, San Diego, California 92182, U.S.A.
Chapter 6. Synthesis and uses of alkyl hydroperoxides and dialkyl peroxidesRoger A. SheldonOce-Andeno B. V., Venlo, The Netherlands
Chapter 7. Singlet oxygen in peroxide chemistryAryeh A. FrimerDepartment of Chemistry, Bar-Ilan University, Ramat-Gan, Israel
Chapter 8. Free-radical reaction mechanisms involving peroxides in solutionJ. A. HowardDivision of Chemistry, National Research Council of Canada, Ottawa K1A OR9, Canada
Chapter 9. Organic sulphur and phosphorus peroxidesRobert V. HoffmanDepartment of Chemistry, New Mexico State University, Las Cruces, New Mexico 88003, U.S.A.
Chapter 10. Diacyl peroxides, peroxycarboxylic acids and peroxy estersGunter BouillonFachrichtung 14.1–Organische Chemie, Universitat des Saarlandes, D-6600 Saarbrucken, W. Germany
Carlo LickFachrichtung 14.1–Organische Chemie, Universitat des Saarlandes, D-6600 Saarbrucken, W. Germany
Kurt SchankFachrichtung 14.1–Organische Chemie, Universitat des Saarlandes, D-6600 Saarbrucken, W. Germany
Chapter 11. EndoperoxidesIsao SaitoDepartment of Synthetic Chemistry, Faculty of Engineering, Kyoto University, Kyoto, Japan
S. Sarma NittalaDepartment of Synthetic Chemistry, Faculty of Engineering, Kyoto University, Kyoto, Japan
Chapter 12. Structural aspects of organic peroxidesJ. Z. GougoutasDepartment of Chemistry, University of Minnesota, Minneapolis, MN 55455, U.S.A.
Chapter 13. Polymeric peroxidesRay CeresaPolymer Consultant, Pepys Cottage, 13 High Street, Cottenham, Cambridge CB44SA, England
55
Chapter 14. Organic reactions involving the superoxide anionAryeh A. FrimerDepartment of Chemistry, Bar-Ilan University, Ramat-Gan, Israel
Chapter 15. Transition-metal peroxides—synthesis and use as oxidizing agentsHubert MimounLaboratoire d’Oxydation, Institut Francais du Petrole, 92506 Rueil-Malmaison, France
Chapter 16. Organic polyoxidesBozo PlesnicarUniversity of Ljubljana, Ljubljana, Yugoslavia
Chapter 17. Polar reaction mechanisms involving peroxides in solutionBozo PlesnicarUniversity of Ljubljana, Ljubljana, Yugoslavia
Chapter 18. Preparation and uses of isotopically labelled peroxidesShigeru OaeDepartment of Chemistry, The University of Tsukuba, Sakura-mura, Niihari-gun, Ibaraki-ken, 305 Japan
Ken FujimoriDepartment of Chemistry, The University of Tsukuba, Sakura-mura, Niihari-gun, Ibaraki-ken, 305 Japan
Chapter 19. Ozonation of single bondsEhud KeinanDepartment of Organic Chemistry, The Weizmann Institute of Science, Rehovot, 76100, Israel
Haim T. VarkonyDepartment of Organic Chemistry, The Weizmann Institute of Science, Rehovot, 76100, Israel
Chapter 20. Pyrolysis of peroxides in the gas phaseLeslie BattDepartment of Chemistry, University of Aberdeen, Aberdeen AB9 2UE, Scotland
Michael T. H. LiuDepartment of Chemistry, University of Prince Edward Island, Charlottetown, Prince Edward Island, C1A4P3, Canada
Chapter 21. Photochemistry and radiation chemistry of peroxidesYoshiro OgataDepartment of Applied Chemistry, Faculty of Engineering, Nagoya University, Nagoya, Japan
Kohtaro TomizawaDepartment of Applied Chemistry, Faculty of Engineering, Nagoya University, Nagoya, Japan
Kyoji FurutaDepartment of Applied Chemistry, Faculty of Engineering, Nagoya University, Nagoya, Japan
Chapter 22. Solid-state reactions of peroxidesM. LazarPolymer Institute of the Slovak Academy of Sciences, 80934 Bratisiava, Czechoslovakia
Chapter 23. Organometallic peroxidesP. B. BrindleyKingston Polytechnic, Kingston upon Thames KT1 2EE, England
56
Chapter 24. Four-membered ring peroxides: 1,2-dioxetanes and a-peroxylactonesWaldemar AdamInstitut fur Organische Chemie, Universitat Wurzburg, Am Hubland, D-8700 Wurzburg, BRDDepartamento de Quimica, Universidad de Puerto Rico, Rio Piedras, Puerto Rico 00931, U.S.A.
The Chemistry of Triple-Bonded Functional Groups, Part 1 (1983)Edited by Saul Patai and Zvi Rappoport
Chapter 1. Chiroptical of compounds containing triple-bonded functional groupsWolfgang RungeOrganisch-Chemisches Institut der Technischen Universitat Munchen, Munchen, Germany
Chapter 2. Thermochemistry of the cyano and isocvano groupsLeslie BattDepartment of Chemistry, University of Aberdeen, Meston Walk, Old Aberdeen, AB9 2UE, Scotland
Chapter 3. Mass spectra of cyano, isocyano and diazo compoundsKlaus-Peter ZellerInstitut fur Organische Chemie, Universitat Tubingen, Auf der Morgenstelle, D-7400 Tubingen, Germany
Chapter 4. Infrared spectra of cyano and isocyano groupsI. N. JuchnovskiInstitute of Organic Chemistry, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria
I. G. BinevInstitute of Organic Chemistry, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria
Chapter 5. Photoelectron spectra of cyano compoundsH. StafastChemische Institute der Universitat Frankfurt, Niederurseler Hang, D-6000 Frankfurt/Main 50,W. Germany
H. BockChemische Institute der Universitat Frankfurt, Niederurseler Hang, D-6000 Frankfurt/Main 50,W. Germany
Chapter 6. Radiation chemistry of triple-bonded moleculesZeev B. AlfassiDepartment of Nuclear Engineering, Ben-Gurion University of the Negev, Beer Sheva, Israel, 84120
Chapter 7. Electrochemistry of the cyano groupKunihisa YoshidaDepartment of Chemistry, Faculty of Engineering Science, Osaka University, Toyonaka, Osaka 560, Japan
Chapter 8. The directing and activating effects of triply bonded groupsMarvin ChartonPratt Institute, Department of Chemistry, Brooklyn, New York 11205, U.S.A.
Chapter 9. Biological formation and metabolic transformations of compounds containing the cyanogroupJ. P. FerrisRensselaer Polytechnic Institute, Troy, N.Y., U.S.A.
57
Chapter 10. Free-radical reactions involving the C−C groupY. AmielThe Weizmann Institute of Science, Rehovot, Israel
Chapter 11. ArynesThomas L. GilchristDepartment of Organic Chemistry, University of Liverpool, England
Chapter 12. Six-membered didehydroheteroarenesH. C. Van Der PlasLaboratory of Organic Chemistry, Landbouwhogeschool, Wageningen, The Netherlands
F. RoeterdinkLaboratory of Organic Chemistry, Landbouwhogeschool, Wageningen, The Netherlands
Chapter 13. Oxidation of triple-bonded groupsLaszlo I. SimandiCentral Research Institute for Chemistry, Budapest, Hungary
Chapter 14. Reduction of triple-bonded groupsRobert O. HutchinsDrexel University, Philadelphia, Pennsylvania, U.S.A.
Mary Gail K. HutchinsTemple University, Philadelphia, Pennsylvania, U.S.A.
Chapter 15. Dediazoniations of arenediazonium ions and related compoundsHeinrich ZollingerTechnisch-Chemisches Laboratorium, Eidgenossische Technische Hochschule (ETH), Zurich, Switzerland
Chapter 16. Alkenediazonium compoundsKaspar BottHauptlaboratorium der BASF Aktiengesellschaft, D-6700 Ludwigshafen, Federal Republic of Germany
Chapter 17. Acidity and proton transfer of cyanocarbon acidsFrank HibbertDepartment of Chemistry, King’s College, Strand, London WC2R 2LS, England
Chapter 18. Recent developments on nitrile oxides, nitrile sulphides and nitrile selenidesGiorgio BianchiInstitute of Organic Chemistry, University of Pavia, Italy
Remo GandolfiInstitute of Organic Chemistry, University of Pavia, Italy
Paolo GrunangerInstitute of Organic Chemistry, University of Pavia, Italy
Chapter 19. Conformation of cyano and isocyano compoundsC. A. KingsburyDepartment of Chemistry, University of Nebraska, Lincoln, NE 68588, U.S.A.
Chapter 20. Recent advances in isocyanide chemistryH. M. WalborskyFlorida State University, Tallahassee, Florida, U.S.A.
58
M. P. PeriasamyMallinckrodt, Inc., St Louis, Missouri, U.S.A.
Chapter 21. Complexation of aryldiazonium ions by polyethersRichard A. BartschDepartment of Chemistry, Texas Tech University, Lubbock, Texas 79409, U.S.A.
Chapter 22. Poly(diacetylenes) and polyyne polymers containing transition-metal atoms in themain chainWilliam D. HuntsmanOhio University, Athens, Ohio, U.S.A.
Chapter 23. Cyclodimerization of alkynes and reactivity of aluminium halide s complexes ofcyclobutadienesHepke HogeveenDepartment of Organic Chemistry, The University, Nijenborgh 16, 9747 AG Groningen, The Netherlands
Douwe M. KokDepartment of Organic Chemistry, The University, Nijenborgh 16, 9747 AG Groningen, The Netherlands
Chapter 24. Structure of triple-bonded moleculesJ. B. MoffatDepartment of Chemistry and Guelph-Waterloo Centre for Graduate Work in Chemistry, University ofWaterloo, Waterloo, Ontario, Canada
Chapter 25. NMR spectra of acetylenesD. G. MorrisDepartment of Chemistry, University of Glasgow, Glasgow G12 8QQ, U.K.
Chapter 26. Preparation and synthetic applications of cyano compoundsAlexander J. FatiadiCentre for Analytical Chemistry, National Measurement Laboratory, National Bureau of Standards,Washington, D.C. 20234, U.S.A.
Chapter 27. General and theoretical properties of triple-bonded moleculesJ. B. MoffatDepartment of Chemistry and Guelph-Waterloo Centre for Graduate Work in Chemistry, University ofWaterloo, Waterloo, Ontario, Canada
Chapter 28. Recent advances in the synthesis of triple-bonded groupsKlaus FriedrichChemisches Laboratorium, Albert-Ludwigs-Universitat, Albertstrasse 21, 7800 Freiburg i. Br., Germany
The Chemistry of the Metal—Carbon Bond, Volume 2 (1985) (See Volume 1 in 1983, Volume 3in 1985, Volume 4 in 1987, Volume 5 in 1989)
Edited by Frank R. Hartley and Saul Patai
Chapter 1. Electrochemical cleavage of metal—carbon bondsC. J. PickettARC Unit of Nitrogen Fixation, University of Sussex, Brighton, East Sussex BN1 9RQ, UK
59
Chapter 2. Heterolytic cleavage of main group metal—carbon bondsMichael H. AbrahamChemistry Department, University of Surrey, Guildford, Surrey GU2 5XH, UK
Priscilla L. GrellierChemistry Department, University of Surrey, Guildford, Surrey GU2 5XH, UK
Chapter 3. Homolytic cleavage of metal—carbon bonds: Groups I to VPhilip J. BarkerResearch School of Chemistry, Australian National University, P.O. Box 4, Canberra, A.C.T. 2600,Australia
Jeremy N. WinterDepartment of Chemistry, University of York, Heslington, York YO1 5DD, UK
Chapter 4. Insertions into main group metal–carbon bondsJ. L. WardellDepartment of Chemistry, University of Aberdeen, Meston Walk, Old Aberdeen AB9 2UE, Scotland, UK
E. S. PatersonDepartment of Chemistry, University of Aberdeen, Meston Walk, Old Aberdeen AB9 2UE, Scotland, UK
Chapter 5. Insertions into transition metal—carbon bondsJohn J. AlexanderDepartment of Chemistry, University of Cincinnati, Cincinnati, Ohio 45221, USA
Chapter 6. Nucleophilic attack on transition metal organometallic compoundsLouis S. HegedusDepartment of Chemistry, Colorado State University, Fort Collins, Colorado 80523, USA
Chapter 7. Electrophilic attack on transition metal μ1-organometallic compoundsM. D. JohnsonDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H OAJ, UK
Chapter 8. Transition metal—carbon bond cleavage through ß-hydrogen eliminationR. J. CrossChemistry Department, The University, Glasgow G12 8QQ, Scotland, UK
Chapter 9. Oxidative addition and reductive eliminationJ. K. StilleDepartment of Chemistry, Colorado State University, Fort Collins, Colorado 80523, USA
Chapter 10. Structure and bonding of main group organometallic compoundsJohn P. OliverDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202, USA
The Chemistry of the Metal—Carbon Bond, Volume 3 (1985) (See Volume 1 in 1983, Volume 2in 1985, Volume 4 in 1987, Volume 5 in 1989)
Edited by Frank R. Hartley and Saul Patai
Chapter 1. Carbon—carbon bond formation using tin and lead organometallicsV. G. Kumar DasChemistry Department, University of Malaya, Kuala Lumpur 22-11, Malaysia
60
Chit-Kay ChuChemistry Department, University of Malaya, Kuala Lumpur 22-11, Malaysia
Chapter 2. Carbon—carbon bond formation using organometallic compounds of zinc, cadmium,and mercuryLeone MiginiacLaboratoire de Synthe se Organique, Universite de Poitiers, 40 Avenue du Recteur Pineau, 86022 Poitiers,France
Chapter 3a. Part 1. η3-Allylnickel complexesG. Paolo ChiusoliIstituto di Chimica Organica dell’Universita, via M. D’Azeglio 85, 43100 Parma, Italy
Giuseppe SalernoDipartimento di Chimica, Universita della Calabria, Arcavacata di Rende, Cosenza, Italy
Chapter 3b. Part 2. η3-Allylpalladium complexesJiro TsujiDepartment of Chemical Engineering, Tokyo Institute of Technology, Meguro, Tokyo 152, Japan
Chapter 3c. Part 3. Other η3-allyl transition metal complexesFumie SatoDepartment of Chemical Engineering, Tokyo Institute of Technology, Meguro, Tokyo 152, Japan
Chapter 4. Olefin oligomerizationOlav-T. OnsagerLaboratory of Industrial Chemistry, Norwegian Institute of Technology, University of Trondheim, N-7034Trondheim-NTH, Norway
Jon Eigill JohansenDivision of Applied Chemistry, SINTEF, N-7034 Trondheim-NTH. Norway
Chapter 5. Alkyne oligomerizationMark J. WinterDepartment of Chemistry, The University, Sheffield S3 7HF, UK
Chapter 6. Transition metal carbonyls in organic synthesisJulian A. DaviesDepartment of Chemistry, College of Arts and Sciences, University of Toledo, Toledo, Ohio 43606, USA
Randy J. ShaverDepartment of Chemistry, College of Arts and Sciences, University of Toledo, Toledo, Ohio 43606, USA
Chapter 7. Olefin and alcohol carbonylationGordon K. AndersonDepartment of Chemistry, University of Missouri-St. Louis, St. Louis, Missouri 63121, USA
Julian A. DaviesDepartment of Chemistry, College of Arts and Sciences, University of Toledo, Toledo, Ohio 43606, USA
Chapter 8. Olefin hydroformylationJulian A. DaviesDepartment of Chemistry, College of Arts and Sciences, University of Toledo, Toledo, Ohio 43606, USA
61
Chapter 9. The Fischer—Tropsch synthesisG. Henrici-OliveDepartment of Chemistry, University of California at San Diego, La Jolla, California 92093, USA
S. OliveDepartment of Chemistry, University of California at San Diego, La Jolla, California 92093, USA
Chapter 10. Olefin carbonylationDonald M. FentonScience and Technology Division, Union Oil Company of California, P.O. Box 76, Brea, California 92621,USA
Eric L. MooreheadScience and Technology Division, Union Oil Company of California, P.O. Box 76, Brea, California 92621,USA
The Chemistry of Organic Selenium and Tellurium Compounds, Volume 1 (1986)(See Volume 2 in 1987, Volume 3 in 2012)
Edited by Saul Patai and Zvi Rappoport
Chapter 1. Organic derivatives of sulphur, selenium and tellurium—an overviewKai Arne JensenUniversity of Copenhagen, Chemical Laboratory II, The H. C. Ørsted Institute, Copenhagen, Denmark
Anders KjærDepartment of Organic Chemistry, The Technical University of Denmark, Lyngby, Denmark
Chapter 2. General and theoretical aspects of organic compounds containing selenium or telluriumRaymond A. PoirierDepartment of Chemistry, Memorial University of Newfoundland, St. John’s, Newfoundland, AIB 3X7,Canada
Imre G. CsizmadiaDepartment of Chemistry, University of Toronto, Toronto, M5S 1A1, Canada
Chapter 3. Structural chemistry of organic compounds containing selenium or telluriumIstvan HargittaiHungarian Academy of Sciences, Research Laboratory for Inorganic Chemistry, Department of StructuralStudies, P.O. Box 117, Budapest, H-1431, Hungary
Bela RozsondaiHungarian Academy of Sciences, Research Laboratory for Inorganic Chemistry, Department of StructuralStudies, P.O. Box 117, Budapest, H-1431, Hungary
Chapter 4. Thermochemistry of selenium and tellurium compoundsL. BattAberdeen University, Aberdeen, Scotland
Chapter 5. Detection and determination of organic selenium and tellurium compoundsKurt J. IrgolicThe Hebrew University, Jerusalem
Dipankar ChakrabortiDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, USA
62
Chapter 6. Nuclear magnetic resonance and electron spin resonance studies of organic selenium andtellurium compoundsNarender P. LuthraDepartment of Chemistry, University of South Carolina, Columbia, South Carolina 29208, USA
Jerome D. OdomDepartment of Chemistry, University of South Carolina, Columbia, South Carolina 29208, USA
Chapter 7. Mass spectrometry of organic selenium and tellurium compoundsGeorge D. SturgeonDepartment of Chemistry, University of Nebraska, Lincoln, Nebraska 68588-0304, USA
Michael L. GrossDepartment of Chemistry, University of Nebraska, Lincoln, Nebraska 68588-0304, USA
Chapter 8. Radiation chemistry of organic selenium and tellurium compoundsRoberto BadielloC. N. R., Servizio Regionale di Sicurezza del Lavoro e Protezione Sanitaria, Facolta di Farmaciadell’Universita di Bologna, Italy
Chapter 9. Selenium-stabilized carbenium ions and free radicalsLaszlo HevesiDepartment of Chemistry, Faculte s Universitaires Notre-Dame de la Paix, 61, Rue de Bruxelles, B-5000Namur, Belgium
Chapter 10. Selenium- and tellurium-containing organic polymersY. OkamotoDepartment of Chemistry, Polytechnic Institute of New York, 333 Jay Street, Brooklyn, New York 11201,USA
Chapter 11. Organometallic compounds with selenium and tellurium atoms bonded to main groupelements of Groups IIIa, IVa and VaRalph A. ZingaroDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, USA
Chapter 12. Synthesis and uses of isotopically labelled selenium and tellurium compoundsKen FujimoriDepartment of Chemistry, The University of Tsukuba, Sakura-mura Niihari-gun, Ibarakiken, 305 Japan
Shigeru OaeOkayamya University of Science, Ridai-cho 1-1, Okayama, 700 Japan
Chapter 13. Selenium and tellurium heterocyclesMarcel RensonUniversite de Liege, Institut de Chimie, Sart-Tilman, 4000 Liege, Belgium
Chapter 14. Tetra- and higher-valent (hypervalent) derivatives of selenium and telluriumJ. BergmanDepartment of Organic Chemistry, Royal Institute of Technology, S-100 44 Stockholm, Sweden
L. EngmanDepartment of Organic Chemistry, Royal Institute of Technology, S-100 44 Stockholm, Sweden
J. SidenDepartment of Organic Chemistry, Royal Institute of Technology, S-100 44 Stockholm, Sweden
63
Chapter 15. Directing and activating effects involving selenium and telluriumFrancesco FringuelliDipartimento di Chimica, Universita di Perugia, Perugia, Italy
Aldo TaticchiDipartimento di Chimica, Universita di Perugia, Perugia, Italy
Chapter 16. Functional groups containing selenium and tellurium in various oxidation statesSonoda NoboruDepartment of Applied Chemistry, Osaka University, Suita, Osaka, Japan
Akiya OgawaDepartment of Applied Chemistry, Osaka University, Suita, Osaka, Japan
Chapter 17. Stereochemistry and chiroptical properties of organic selenium and telluriumcompoundsGunther SnatzkeLehrstuhl fur Strukturchemie, Ruhruniversitat Bochum, POB 10 21 48, D-4630 Bochum, FRG
Chapter 18. Ligand properties of organic selenium and tellurium compoundsHenry J. GyslingResearch Laboratories, Eastman Kodak Company, Rochester, New York 14650, USA
The Chemistry of the Cyclopropyl Group, Volume 1 (1987) (See Volume 2 in 1995)
Edited by Zvi Rappoport
Chapter 1. Structures, Energies and Spectra of CyclopropanesKenneth B. WibergDepartment of Chemistry, Yale University, New Haven, Connecticut 06511, USA
Chapter 2. Chiroptical Properties of Cyclopropane DerivativesWolfgang RungeInstitut fur Struktur- und Systemforschung, Wormser Str. 5, D-6900 Heidelberg, West Germany
Chapter 3. Nuclear Magnetic Resonance and Infrared Spectra of Cyclopropanes and CyclopropenesD. G. MorrisDepartment of Chemistry, University of Glasgow, Glasgow G12 8QQ, UK
Chapter 4. The Chemistry of Ionized Cyclopropanes in the Gas PhaseHelmut SchwarzInstitut fur Organische Chemie, Technische Universitat Berlin, D-1000 Berlin 12, West Germany
Chapter 5. Photoelectron SpectroscopyRoy Ernest BallardSchool of Chemical Sciences, University of East Anglia, Norwich, Norfolk, England
Chapter 6. Acidity and Basicity of CyclopropanesMerle A. BattisteUniversity of Florida, Gainesville, Florida, USA
James M. CoxonUniversity of Canterbury, Christchurch, New Zealand
64
Chapter 7. Preparation of Cyclopropyl DerivativesTakashi TsujiDepartment of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Hokkaido 060, Japan
Shinya NishidaDepartment of Chemistry, Faculty of Science, Hokkaido University, Sapporo, Hokkaido 060, Japan
Chapter 8. Organic Synthesis via Cyclopropanes: Principles and ApplicationsHans-Ulrich ReissigInstitut fur Organische Chemie der Universitat Wurzburg, D-8700 Wurzburg, Federal Republic ofGermany Institut fur Organische Chemie und Biochemie der Technischen Hochschnle Darmstadt, D-6100Darmstadt, Germany
Chapter 9. Synthesis and Reactivity of Electrophilic CyclopropanesRoland VerheLaboratory of Organic Chemistry, Faculty of Agricultural Sciences, State University of Gent, CoupureLinks 653, B-9000 Gent, Belgium
Norbert de KimpeLaboratory of Organic Chemistry, Faculty of Agricultural Sciences, State University of Gent, CoupureLinks 653, B-9000 Gent, Belgium
Chapter 10. Conjugative and Substituent Properties of the Cyclopropyl GroupThomas T. TidwellDepartment of Chemistry, University of Toronto, Scarborough Campus, Scarborough, Ontario, CanadaM1C 1A4
Chapter 11. Solvolysis of Cyclopropyl-Substituted DerivativesEdwin C. FriedrichDepartment of Chemistry, University of California, Davis, California 95616 USA
Chapter 12. Cyclopropyl Radicals, Anion Radicals and AnionsGernot BocheFachbereich Chemie, Philipps-Universitat Marburg, D-3550 Marburg, Federal Republic of Germany
Harry M. WalborskyChemistry Department, Florida State University, Tallahassee, Florida 32306-3006, USA
Chapter 13. Rearrangements Involving the Cyclopropyl GroupJacques SalaunLaboratoire des Carbocycles, UA 478 du CNRS, Universite de Paris-Sud, 91405 Orsay Cedex, France
Chapter 14. Radiation Chemistry and Hot Atom Chemistry of Cyclopropane and Its DerivativesZeev B. AlfassiDepartment of Nuclear Engineering, Ben Gurion University of the Negev, Beer Sheva 84102, Israel
Chapter 15. Electrochemistry of the Cyclopropyl GroupJames Y. BeckerDepartment of Chemistry, Ben-Gurion University of the Negev, Beer Sheva, Israel 84120
Chapter 16. Biochemistry of the Cyclopropyl GroupHung-Wen LiuDepartment of Chemistry, University of Minnesota, Minneapolis, MN.55455, USA
65
Christopher T. WalshDepartments of Chemistry and Biology, Massachusetts Institute of Technology, Cambridge, MA 02139,USA
Chapter 17. Preparation and Uses of Isotopically Labeled DerivativesBarry K. CarpenterDepartment of Chemistry, Cornell University, Ithaca, New York 14853-1301, USA
Chapter 18. Cyclopropanes Having Extra StrainJoel F. LiebmanDepartment of Chemistry, University of Maryland Baltimore County, Catonsville, Maryland 21228, USA
Arthur GreenbergDepartment of Chemical Engineering and Chemistry, New Jersey Institute of Technology, Newark,New Jersey 07102, USA
Chapter 19. Bicyclo[1.1.0]ButaneShmaryahu HozBar-Ilan University, Ramat-Gan, Israel
Chapter 20. [m.n.1] Propellanes
David GinsburgDepartment of Chemistry, Technion—Israel Institute of Technology, Haifa 32000, Israel
Chapter 21. CyclopropenesBrian HaltonDepartment of Chemistry, Victoria University of Wellington, New Zealand
Martin G. BanwellDepartment of Chemistry, University of Auckland, New Zealand
Chapter 22. AminocyclopropanesE. VilsmaierFachbereich Chemie, Universitat Kaiserslautern, D-6750 Kaiserslautern, West Germany
Chapter 23. The Chemistry of CyclopropanonesHarry H. WassermanDepartment of Chemistry, Yale University, New Haven, Connecticut 06511, USA
Donald R. BerdahlDepartment of Chemistry, Yale University, New Haven, Connecticut 06511, USA
Ta-Jung LuDepartment of Chemistry, Yale University, New Haven, Connecticut 06511, USA
Chapter 24. Cyclopropenyl CompoundsW. E. BillupsDepartment of Chemistry, Rice University, Houston, Texas 77251, USA
A. W. MooreheadDepartment of Chemistry, Rice University, Houston, Texas 77251, USA
66
The Chemistry of the Metal—Carbon Bond, Volume 4 (1987) (See Volume 1 in 1983, Volume 2in 1985, Volume 3 in 1985, Volume 5 in 1989)
Edited by Frank R. Hartley
Chapter 1. Preparation and use in organic synthesis of organolithium and Group IAorganometallicsJ. L. WardellDepartment of Chemistry, University of Aberdeen, Meston Walk, Old Aberdeen AB9 2UE, Scotland, UK
Chapter 2. Preparation and use of Grignard and Group II organometallics in organic synthesisC. L. RastonDepartment of Physical and Inorganic Chemistry, University of Western Australia, Nedlands, WesternAustralia, 6009
G. SalemResearch School of Chemistry, Australian National University, Canberra, A.C.T. 2600, Australia
Chapter 3. Preparation and use of organoboranes in organic synthesisD. S. MattesonDepartment of Chemistry, Washington State University, Pullman, Washington 99164-4630, USA
Chapter 4. Preparation and use of organoaluminium compounds in organic synthesisP. A. ChalonerSchool of Chemistry and Molecular Sciences, University of Sussex, Falmer, Brighton BNI 9QJ, UK
Chapter 5. Preparation and use of organothallium (III) compounds in organic synthesisS. UemuraInstitute for Chemical Research, Kyoto University, Uji, Kyoto 611, Japan
Chapter 6. Preparation and use of organosilicon compounds in organic synthesisE. W. ColvinChemistry Department, University of Glasgow, Glasgow G12 8QQ, UK
Chapter 7. Use of organoiron compounds in organic synthesisDidier AstrucLaboratoire de Chimie Organique et Organometallique, U.A. CNRS No. 35, Universite de Bordeaux I, 351Cours de la Liberation, 33405 Talence Cedex, France
Chapter 8. Use of organorhodium compounds in organic synthesisF. H. JardineDepartment of Chemistry, North East London Polytechnic, Romford Road, London E15 4LZ, UK
Chapter 9. Use of organonickel compounds in organic synthesisK. TamaoDepartment of Synthetic Chemistry, Kyoto University, Kyoto 606, Japan
M. KumadaDepartment of Synthetic Chemistry, Kyoto University, Kyoto 606, Japan
Chapter 10. Transition metal-stabilized carbocations in organic synthesisA. J. PearsonDepartment of Chemistry, Case Western Reserve University, Cleveland, Ohio 44106, USA
67
Chapter 11. HydrogenationD. ParkerDepartment of Chemistry, University Science Laboratories, South Road, Durham, DH1 3LE, UK
Chapter 12. Mechanism of homogeneous hydrogenationF. H. JardineDepartment of Physical Sciences, North East London Polytechnic, Romford Road, London E15 4LZ, UK
Chapter 13. Saturated carbon—hydrogen bond activationJ. R. ChipperfieldDepartment of Chemistry, The University, Hull HU6 7RX, UK
D. E. WebsterDepartment of Chemistry, The University, Hull HU6 7RX, UK
Chapter 14. Supported metal complex catalystsF. R.HartleyRoyal Military College of Science, Shrivenham, Swindon, Wiltshire SN6 8LA, UK
The Chemistry of Organic Selenium and Tellurium Compounds, Volume 2 (1987)(See Volume 1 in 1986, Volume 3 in 2012)
Edited by Saul Patai and Zvi Rappoport
Chapter 1. Photoelectron spectroscopy of organic derivatives containing selenium and telluriumCarla CaulettiDipartimento di Chimica, Universita La Sapienza di Roma, Piazzale Aldo Moro 5, 00185 Rome, Italy
Giuseppe DistefanoIstituto dei Composti del Carbonic Contenenti Eteroatomi e loro Applicazioni, Ozzano Emilia, Via Tolaradi Sotto 89, 40064 Ozzano Emilia, Italy
Chapter 2. The application of Mossbauer spectroscopy to the study of organotellurium compoundsFrank J. BerryDepartment of Chemistry, University of Birmingham, Birmingham B15 2TT, UK
Chapter 3. Preparative uses of organoselenium and organotellurium compoundsThomas G. BackDepartment of Chemistry, University of Calgary, Calgary, Alberta, Canada, T2N 1N4
Chapter 4. Seleno- and telluro-carbonyl compoundsFrank S. Guziec Jr.Department of Chemistry, New Mexico State University, Las Cruces, New Mexico 88003, USA
Chapter 5. Photochemistry of organic compounds of selenium and telluriumZeev GoldschmidtDepartment of Chemistry, Bar Ilan University, Ramat-Gen, Israel
Chapter 6. Acidity, hydrogen bonding and self-association in organic and organometalliccompounds of selenium and telluriumThomas B. RauchfussSchool of Chemical Sciences, University of Illinois, Urbana, Illinois 61801, USA
68
Chapter 7. Biochemistry of physiologically active selenium compoundsKenji SodaInstitute for Chemical Research, Kyoto University, Uji, Kyoto-Fu 611, Japan
Hidehiko TanakaInstitute for Chemical Research, Kyoto University, Uji, Kyoto-Fu 611, Japan
Nobuyoshi EsakiInstitute for Chemical Research, Kyoto University, Uji, Kyoto-Fu 611, Japan
Chapter 8. Biological and biochemical aspects of tellurium derivativesTsvi SadehInstitute of Chemical Research, University of Kyoto, Uji, Kyoto-Fu 611, Japan
Chapter 9. Pharmacological and toxicological aspects of inorganic and organic selenium compoundsTohru MasukawaDepartment of Pharmacology, Faculty of Pharmaceutical Sciences, Setsunan University, 45-1,Nagaotoge-cho, Hirakata, Osaka 573-01, Japan
Chapter 10. Insertion and extrusion reactionsLars HenriksenDepartment of General and Organic Chemistry, The H. C. Ørsted Institute, University of Copenhagen,DK-2100 Copenhagen, Denmark
Chapter 11. Compounds with Se−N and Te−N bondsG. KirschLaboratoire de Carbochimie et Synthese Organique, Universite de Metz, Faculte des Sciences, Ile duSaulcy, 57045-Metz Cedex, France
L. ChristiaensInstitut de Chimie Organique, Universite de Liege, Sart-Tilman, 4000-Liege, Belgium
Chapter 12. Synthesis of organic conductors containing selenium and telluriumD. CowanThe Johns Hopkins University, Baltimore, Maryland, USA
A. KiniThe Johns Hopkins University, Baltimore, Maryland, USA
Chapter 13. Organoselenium and organotellurium analogues of ethers and peroxidesWilliam R. McWhinnieDepartment of Molecular Sciences, Aston University, Aston Triangle, Birmingham B4 7ET, UK
Chapter 14. Organic selenocyanates and tellurocyanates and related compoundsAkio ToshimitsuInstitute for Chemical Research, Kyoto University, Uji, Kyoto 611, Japan
Sakae UemuraInstitute for Chemical Research, Kyoto University, Uji, Kyoto 611, Japan
Chapter 15. Organic compounds containing bonds between Se or Te with P, As, Sb and BiWolf-Walther Du MontFachbereich Chemie, Universitat Oldenburg, Carl-von-Ossietzky-Strasse 9-11, D-2900 Oldenburg, FRG
Ralph HenselFachbereich Chemie, Universitat Oldenburg, Carl-von-Ossietzky-Strasse 9-11, D-2900 Oldenburg, FRG
69
Silvia KubiniokFachbereich Chemie, Universitat Oldenburg, Carl-von-Ossietzky-Strasse 9-11, D-2900 Oldenburg, FRG
Lutz LangeFachbereich Chemie, Universitat Oldenburg, Carl-von-Ossietzky-Strasse 9-11, D-2900 Oldenburg, FRG
Chapter 16. Free radical reactions of organoselenium and organotellurium compoundsLaurence CastleDepartment of Chemistry, Royal Holloway and Bedford New College, University of London, Egham,Surrey TW20 OEX, UK
M. John PerkinsDepartment of Chemistry, Royal Holloway and Bedford New College, University of London, Egham,Surrey TW20 OEX, UK
Chapter 17. Synthesis of selenium and tellurium ylides and carbanions: application to organicsynthesisA. KriefUniversitaires Notre-Dame Facultes de la Paix, Namur, Belgium
Chapter 18. Selenium and tellurium derivatives of carbohydrates and nucleoside analogsZbigniew J. WitczakWhistler Center For Carbohydrate Research, Purdue University, Smith Hall, West Lafayette, Indiana47907, USA
The Chemistry of α-Haloketones, α-Haloaldehydes and α-Haloimines (1988)Edited by Norbert de Kimpe and Roland Verhe
Chapter 1. Synthesis and reactivity of α-halogenated ketones
Appendix to Chapter 1: Synthesis and reactivity of α-halogenated ketones
Chapter 2. α-Halogenated imines
Appendix to Chapter 2: α-Halogenated imines
Chapter 3. Synthesis and reactivity of α-halogenated aldehydes
The Chemistry of Quinonoid Compounds, Volume 2, Part 1 (1988) (See Volume 1 in 1974)
Edited by Saul Patai and Zvi Rappoport
Chapter 1. General and theoretical aspects of quinonesAnne SkanckeDepartment of Chemistry, University of Tromsø, P.O.B. 953, N-9001 Tromsø, Norway
Per N. SkanckeDepartment of Chemistry, University of Tromsø, P.O.B. 953, N-9001 Tromsø, Norway
70
Chapter 2. Physical and chemical analysis of quinonesS. BergerFachbereich Chemie der Universitat Marburg, D-355 Marburg, Germany
P. HertlInstitut fur Organische Chemie der Universitat Tubingen, D-7400 Tubingen, Germany
A. RiekerInstitut fur Organische Chemie der Universitat Tubingen, D-7400 Tubingen, Germany
Chapter 3. Mass spectra of quinonesKlaus-Peter ZellerInstitut fur Organische Chemie, Universitat Tubingen, Auf der Morgenstelle, D-7400 Tubingen, FRG
Roland MullerInstitut fur Organische Chemie, Universitat Tubingen, Auf der Morgenstelle, D-7400 Tubingen, FRG
Chapter 4. Chiroptical properties and absolute configurations of chiral quinonesHoward E. SmithDepartment of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, USA
Chapter 5. Photoelectron spectra of quinonoid compoundsL. KlasincDepartment of Chemistry, Louisiana State University, Baton Rouge, Louisiana 70803, USA
S. P. McGlynnRudjer Boskovic Institute, Zagreb, Croatia, Yugoslavia
Chapter 6. Photochromism and thermochromism in bianthrones and bianthrylidenesK. A. MuszkatDepartment of Structural Chemistry, the Weizmann Institute of Science, Rehovot, Israel
Chapter 7. Chemiluminescence of quinonoid compoundsKarl-Dietrich GundermannInstitut fur Organische Chemie, Technische Universitat Clausthal, 3392 Clausthal-Zellerfeld,Leibnizstrasse 6, FRG
Dieter LieskeInstitut fur Organische Chemie, Technische Universitat Clausthal, 3392 Clausthal-Zellerfeld,Leibnizstrasse 6, FRG
Chapter 8. Recent advances in the synthesis of quinonoid compoundsYoshinori NarutaDepartment of Chemistry, Faculty of Science, Kyoto University, Kyoto 606, Japan
Kazuhiro MaruyamaDepartment of Chemistry, Faculty of Science, Kyoto University, Kyoto 606, Japan
Chapter 9. ortho-Quinonoid compoundsColin W. G. FishwickOrganic Chemistry Department, the University, Leeds LS29JT, U.K.
David W. JonesOrganic Chemistry Department, the University, Leeds LS29JT, U.K.
Chapter 10. meta-Quinonoid compoundsJerome A. BersonDepartment of Chemistry, Yale University, P.O. Box 6666, New Haven, Connecticut 06511-8118, USA
71
Chapter 11. Quinones as synthonesK. Thomas FinleyDepartment of Chemistry, State University College, Brockport, New York 14420, USA
Chapter 12. Electrochemistry of quinonesJames Q. ChambersDepartment of Chemistry, University of Tennessee, Knoxville, TN 37996, USA
Chapter 13. Recent advances in the photochemistry of quinonesKazuhiro MaruyamaDepartment of Chemistry, Faculty of Science, Kyoto University, Kitashirakawa Oiwakecho, Kyoto 606,Japan
Atsuhiro OsukaDepartment of Chemistry, Faculty of Science, Kyoto University, Kitashirakawa Oiwakecho, Kyoto 606,Japan
Chapter 14. Radiation chemistry of quinonoid compoundsP. NetaCenter for Chemical Physics, National Bureau of Standards, Gaithersburg, Maryland 20899, USA
Chapter 15. Chemistry of quinone bis-and monoketalsJohn S. SwentonDepartment of Chemistry, The Ohio State University, Columbus, OH 43210, USA
Chapter 16. Quinhydrones and semiquinonesM. Catherine DepewDepartment of Chemistry, Queen’s University, Kingston, Ontario, Canada K7L 3N6
Jeffrey K. S. WanDepartment of Chemistry, Queen’s University, Kingston, Ontario, Canada K7L 3N6
Chapter 17. Heterocyclic quinonesRichard W. MiddletonThe Cancer Research Campaign’s Gray Laboratory, Northwood, Middlesex, UK and Brunel University,Uxbridge, Middlesex UB8 3PH, UK
John ParrickBrunel University, Uxbridge, Middlesex UB8 3PH, UK
Chapter 18. Polymerization and polymers of quinonoid compoundsShouji IwatsukiDepartment of Chemical Research for Resources, Faculty of Engineering, Mie University, Tsu, Japan
Chapter 19. Isotopically labelled quinonesMieczyslaw ZielinskiIsotope Laboratory, Faculty of Chemistry, Jagiellonian University, Cracow, Poland
Marianna KanskaDepartment of Chemistry, University of Warsaw, Warsaw, Poland
Chapter 20. The solid state photochemistry of tetrahydronaphtho-quinones: Crystalstructure—reactivity relationshipsJohn R. SchefferDepartment of Chemistry, University of British Columbia, Vancouver, Canada, V6T 1Y6
72
James TrotterDepartment of Chemistry, University of British Columbia, Vancouver, Canada, V6T 1Y6
Chapter 21. Quinonediimines, monoimines and related compoundsEric R. BrownColour Negative Technology Division, Photographic Research Laboratories, Eastman Kodak Company,B82 RL, Rochester, New York 14650, USA
Chapter 22. Biochemistry of quinonesHiroyuki InouyeFaculty of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto, Japan
Eckhard LeistnerInstitut fur Pharmazeutische Biologie, Rheinische Friedrich-Wilhelms-Universitat Bonn, Bonn, FRG
Chapter 23. Quinones as oxidants and dehydrogenating agentsHans-Dieter BeckerDepartment of Organic Chemistry, Chalmers University of Technology and University of Gothenburg,S-412 96 Gothenburg, Sweden
Alan B. TurnerDepartment of Organic Chemistry, Chalmers University of Technology and University of Gothenburg,S-412 96 Gothenburg, Sweden
Chapter 24. Azulene quinonesLawrence T. ScottDepartment of Chemistry and Center for Advanced Study, College of Arts and Science, University ofNevada-Reno, Reno, Nevada 89557, USA
Chapter 25. Extended quinonesPeter BoldtInstitut fur Organische Chemie der Technischen Universitat Braunschweig, D-3300 Braunschweig, FRG
Chapter 26. Non-benzenoid quinonesHenry N. C. WongDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong
Tze-Lock ChanDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong
Tien-Yau LuhDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong
The Chemistry of Sulphones and Sulphoxides (1988)Edited by Saul Patai, Zvi Rappoport and Charles Stirling
Chapter 1. General and Theoretical AspectsA. GavezzottiDipartimento di Chimica Fisica e Elettrochimica e Centro CNR, Universita di Milano, Milan, Italy
Chapter 2. Structural Chemistry of Gaseous Sulfoxides and SulfonesIstvan HargittaiStructural Chemistry Research Group of the Hungarian Academy of Sciences, Eotvos University, POBox 117, Budapest, H-1431, Hungary
73
Chapter 3. Stereochemistry, Conformation, and Chiroptical Properties of SulfoxidesKenneth K. AndersenDepartment of Chemistry, University of New Hampshire, Durham, NH 03824, USA
Chapter 4. Thermochemistry of Sulfoxides and SulfonesJohn T. HerronChemical Kinetics Division, National Bureau of Standards, Gaithersburg, MD 20899, USA
Chapter 5. Detection and Determination of Sulphones and SulphoxidesM. R. F. AshworthFachbereich 13.5, Universitat des Saarlandes, D-6600 Saarbrucken, FRG, Germany
Chapter 6. Mass Spectra of Sulfoxides and SulfonesKalevi PihlajaDepartment of Chemistry, University of Turku, SF 20500 Turku 50, Finland
Chapter 7. Synthesis of Open-Chain SulfonesKurt SchankFachrichtung 13.2 Organische Chemie, Universitat des Saarlandes, D-6600 Saarbrucken, FRG, Germany
Chapter 8. Synthesis of SulphoxidesJozef DrabowiczPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, 90-362 Lodz, Boczna 5, Poland
Piotr KielbasinskiPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, 90-362 Lodz, Boczna 5, Poland
Marian MikolajczykPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, 90-362 Lodz, Boczna 5, Poland
Chapter 9. Cyclic Sulfones and SulfoxidesUri ZollerHaifa University, Oranim, Israel
Chapter 10. Electronic Effects of the Sulfinyl and Sulfonyl GroupsJohn ShorterDepartment of Chemistry, The University, Hull, HU6 7RX, UK
Chapter 11. Hydrogen Bonding and Complexing Properties of R2SO2 and R2SONaomichi FurukawaDepartment of Chemistry, The University of Tsukuba, Sakura-mura, Niihari-gun, Ibaraki 305, Japan
Hisashi FujiharaDepartment of Chemistry, The University of Tsukuba, Sakura-mura, Niihari-gun, Ibaraki 305, Japan
Chapter 12. Behavior of a-Sulfinyl and a-Sulfonyl CarbanionsShigeru OaeOkayama University of Science, 1-1 Ridai-cho, Okayama 700, Japan
Yuzuru UchidaDepartment of Applied Chemistry, Osaka Institute of Technology, Asahi-ku, Osaka 535, Japan
74
Chapter 13. Rearrangements Involving SulfonesSamuel BravermanDepartment of Chemistry, Bar-Ilan University, Ramat-Gan 52100, Israel
Chapter 14. Rearrangements Involving SulfoxidesSamuel BravermanDepartment of Chemistry, Bar-Ilan University, Ramat-Gan 52100, Israel
Chapter 15. Synthetic Uses of SulfonesKazuhiko TanakaDepartment of Chemistry, Faculty of Science, Kyoto University, Sakyo, Kyoto 606, Japan
Aritsune KajiDepartment of Chemistry, Faculty of Science, Kyoto University, Sakyo, Kyoto 606, Japan
Chapter 16. Asymmetric Synthesis Using a-Sulfinyl Carbanions and ß-Unsaturated SulfoxidesGary H. PosnerDepartment of Chemistry, The Johns Hopkins University, Baltimore, MD 21218, USA
Chapter 17. Methionine Sulfoxide: Chemistry and BiochemistryNathan BrotRoche Institute of Molecular Biology, Roche Research Center, Nutley, NJ 07110, USA
Herbert WeissbachRoche Institute of Molecular Biology, Roche Research Center, Nutley, NJ 07110, USA
Chapter 18. Photochemistry of Sulfoxides and SulfonesI. W. J. StillDepartment of Chemistry, University of Toronto, Erindale Campus, Mississauga, Ontario, Canada, L5L1C6, Canada
Chapter 19. Radiation Chemistry of Sulfoxides and SulfonesZeev B. AlfassiDepartment of Nuclear Engineering, Ben-Gurion University of the Negev, Beer Sheva 84102, Israel
Chapter 20. Reduction of Sulphoxides and SulphonesJ. Stuart GrossertDepartment of Chemistry, Dalhousie University, Halifax, Nova Scotia, Canada, B3H 4J3, Canada
Chapter 21. Oxidation of Sulphoxides and SulphonesJeffrey HoyleChemistry-Soils Department, Nova Scotia Agricultural College, PO Box 550, Truro, Nova Scotia, Canada,B2N 5E3, Canada
Chapter 22. The Electrochemical Reactivity of Sulphones and SulphoxidesJacques SimonetLaboratoire d’Electrochimie, CNRS, Universite de Rennes 1, France
Chapter 23. Electron Transfer Reactions of Sulfoxides and SulfonesMichel ChanonUniversite d’Aix-Marseille III, Laboratoire de Chimie Inorganique Moleculaire, UA 126-CNRS, 13397Marseille, Cedex 13, France
Andre SamatUniversite d’Aix-Marseille III, Laboratoire de Chimie Inorganique Moleculaire, UA 126-CNRS, 13397Marseille, Cedex 13, France
75
Chapter 24. Sulfinyl RadicalsC. ChatgilialogluIstituto dei composti del carbonio contenti eteroatomi e loro applicazioni, CNR, Ozzano Emilia, Bologna,Italy
Chapter 25. Sulfonyl RadicalsC. ChatgilialogluIstituto dei composti del carbonio contenti eteroatomi e loro applicazioni, CNR, Ozzano Emilia, Bologna,Italy
The Chemistry of Double-Bonded Functional Groups, Volume 2, Part 1 (1989)(See Volume 1 in 1977)
Edited by Saul Patai
Chapter 1. Complementary views on the homopolar double-bond structureGeorges TrinquierLaboratoire de Physique Quantique, CNRS, UA 505, Universite Paul Sabatier, 118, route de Narbonne,31062 Toulouse Cedex, France
Jean-Paul MalrieuLaboratoire de Physique Quantique, CNRS, UA 505, Universite Paul Sabatier, 118, route de Narbonne,31062 Toulouse Cedex, France
Chapter 2. Mass spectrometry of the double bondMargaret N. MruzekDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H OAJ, UK
Chapter 3. Nuclear magnetic resonance spectroscopy of C−C, C−O, C−N and N−N double bondsPoul Erik HansenInstitute of Life Sciences and Chemistry, University of Roskilde, P.O. Box 260, DK-4000 Roskilde,Denmark
Chapter 4. The photoelectron spectroscopy of double-bonded CC, CN, NN and CO groupsL. KlasincDepartment of Chemistry, Louisiana State University, Baton Rouge, LA 70803, USA
S. P. McGlynnDepartment of Chemistry, Louisiana State University, Baton Rouge, LA 70803, USA
Chapter 5. Directing and activating effects of doubly bonded groupsMarvin ChartonChemistry Department, School of Liberal Arts and Sciences, Pratt Institute, Brooklyn, NY 11205, USA
Chapter 6. Double bonds from a biochemical perspectiveAlan H. MehlerDepartment of Biochemistry, Howard University College of Medicine, Washington DC, USA
Chapter 7. Intramolecular 1,3-dipolar cycloadditions to double bondsO. TsugeKumamoto Institute of Technology, Kumamoto 860, Japan
T. HattaKumamoto Institute of Technology, Kumamoto 860, Japan
76
T. HisanoFaculty of Pharmaceutical Sciences, Kumamoto University, Kumamoto 862, Japan
Chapter 8. The ene reactionG. V. BoydDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel
Chapter 9. Radiation chemistry of double-bonded compoundsZeev B. AlfassiDepartment of Nuclear Engineering, Ben Gurion University of the Negev, Beer Sheva 84121, Israel
Chapter 10. Asymmetric induction in additions to C−O and C−N bondsJoseph KleinDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel
Chapter 11. Electrophilic additions to carbon–carbon double bondsGeorge H. SchmidDepartment of Chemistry, University of Toronto, Toronto, Ontario, Canada
Chapter 12. Mechanisms of base-catalyzed alkene-forming 1,2-eliminationsJoseph R. GandlerDepartment of Chemistry, California State University, Fresno, California 93740, USA
Chapter 13. Carbonylation of main-group organometallic compoundsNorma NudelmanDepartamento de Quimica Organica, Facultad de Ciencias Exactas y Naturales, Universidad de BuenosAires, Pab. II, P.3, Ciudad Universitaria, 1428 Buenos Aires, Argentina
Chapter 14. Rearrangements involving allenesSamuel BravermanDepartment of Chemistry, Bar-Ilan University, Ramat Gan 52100, Israel
Chapter 15. 1,1-DiarylalkenesWilliam S. MurphyChemistry Department, University College, Cork, Ireland
Chapter 16. FulvenesM. NeuenschwanderInstitute of Organic Chemistry, University of Bern, CH-3012 Bern, Switzerland
Chapter 17. The thiocarbonyl groupErnst SchaumannInstitut fur Organische Chemie, Universitat Hamburg, D-2000 Hamburg 13, FRG
Chapter 18. Cycloadditions of enonesJanine CossyLaboratoire de Photochimie, Universite de Reims, France
Pierre-Alain CarruptInstitut de Chimie Organique, Universite de Lausanne, Switzerland
Pierre VogelInstitut de Chimie Organique, Universite de Lausanne, Switzerland
77
The Chemistry of Enones, Part 1 (1989)Edited by Saul Patai and Zvi Rappoport
Chapter 1. General and theoreticalA. Y. MeyerDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel
Chapter 2. Structural chemistry of enonesBernd SchweizerInstitute of Organic Chemistry, ETH Zurich, CH-8092 Zurich, Switzerland
Chapter 3. Conformations, chiroptical and related spectral properties of enonesJacek GawronskiFaculty of Chemistry, Adam Mickiewicz University, 60780 Poznan, Poland
Chapter 4. Thermochemistry of enones and related speciesJoel F. LiebmanDepartment of Chemistry, University of Maryland Baltimore County, 5401 Wilkens Avenue, Baltimore, MD21228, USA Center for Advanced Research in Biotechnology, 9600 Gudeslky Drive, Rockville, MD 20850,USA
Ralph M. PollackDepartment of Chemistry, University of Maryland Baltimore County, 5401 Wilkens Avenue, Baltimore, MD21228, USA Center for Advanced Research in Biotechnology, 9600 Gudeslky Drive, Rockville, MD 20850,USA
Chapter 5. NMR spectroscopy of enonesHugo E. GottliebDepartment of Chemistry, Bar-Ilan University, Ramat-Gan 52100, Israel
Chapter 6. The chemistry of ionized enones in the gas phaseFrantisek TurecekThe J. Heyrovsky Institute of Physical Chemistry and Electrochemistry, Czechoslovak Academy ofSciences, Praha, Czechoslovakia
Chapter 7. Synthesis of enonesChachanat ThebtaranonthDepartment of Chemistry, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok 10400, Thailand
Yodhathai ThebtaranonthDepartment of Chemistry, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok 10400, Thailand
Chapter 8. Synthetic uses of enonesGerhard V. BoydDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem, Israel
Chapter 9. Acid–base behaviour of enonesRomuald I. ZalewskiDepartment of General Chemistry, Academy of Economy, Poznan, Poland
Chapter 10. Nucleophilic attacks on enonesDaniele DuvalLaboratoire de Chimie Physique Organique, Universite de Nice, Parc Valrose, 06034 Nice Cedex, France
78
Serge GeribaldiLaboratoire de Chimie Physique Organique, Universite de Nice, Parc Valrose, 06034 Nice Cedex, France
The Chemistry of Enones, Part 1 (1989)Edited by Saul Patai and Zvi Rappoport
Chapter 11. Addition of electrons or radicals to a, ß-unsaturated ketonesGlen A. RussellDepartment of Chemistry, Iowa State University, Ames, Iowa 50011, USA
Chapter 12. The reaction of enones with electrophilesKlaus MullenDepartment of Organic Chemistry, University of Mainz, J. J. Becher-Weg 18-20, D-6500 Mainz, FRG
Peter WolfDepartment of Organic Chemistry, University of Mainz, J. J. Becher-Weg 18-20, D-6500 Mainz, FRG
Chapter 13. Chemical and enzymatic conversion of ß, γ -enones to ß, γ -enonesRalph M. PollackLaboratory for Chemical Dynamics, Department of Chemistry, University of Maryland Baltimore County,Baltimore, MD 21228 USA and Center for Advanced Research in Biotechnology, 9600 Gudelsky Drive,Rockville, MD 20850, USA
Patricia L. BoundsLaboratory for Chemical Dynamics, Department of Chemistry, University of Maryland Baltimore County,Baltimore, MD 21228 USA and Center for Advanced Research in Biotechnology, 9600 Gudelsky Drive,Rockville, MD 20850, USA
Charles L. BevinsLaboratory for Chemical Dynamics, Department of Chemistry, University of Maryland Baltimore County,Baltimore, MD 21228 USA and Center for Advanced Research in Biotechnology, 9600 Gudelsky Drive,Rockville, MD 20850, USA
Chapter 14. Enone electrochemistryR. Daniel LittleDepartment of Chemistry, University of California, Santa Barbara, Santa Barbara, CA 93106, USA
Manuel M. BaizerDepartment of Chemistry, University of California, Santa Barbara, Santa Barbara, CA 93106, USA
Chapter 15. The photochemistry of enonesDavid I. SchusterDepartment of Chemistry, New York University, New York, NY 10003, USA
Chapter 16. Radiation chemistry of enonesP. NetaCenter for Chemical Physics, National Bureau of Standards, Gaithersburg, Maryland 20899, USA
M. DizdarogluCenter for Chemical Physics, National Bureau of Standards, Gaithersburg, Maryland 20899, USA
Chapter 17. The oxygenation of enonesAryeh A. FrimerThe Ethel and David Resnick Chair in Active Oxygen Chemistry, Department of Chemistry, Bar IlanUniversity, Ramat Gan 52100, Israel
79
Chapter 18. Reduction of a, ß-unsaturated carbonyl compoundsEhud KeinanDepartment of Chemistry, Technion—Israel Institute of Technology, Technion City, Haifa 32000, Israel
Noam GreenspoonDepartment of Chemistry, Technion—Israel Institute of Technology, Technion City, Haifa 32000, Israel
Chapter 19. Organometallic derivatives of a, ß-unsaturated enonesJames A. S. HowellChemistry Department, University of Keele, Keele, Staffordshire, ST5 5BG, UK
Chapter 20. Dienols (enolization of enones)Brian CaponChemistry Department, Hong Kong University, Pokfulam Road, Hong Kong
Chapter 21. Asymmetric synthesis with chiral enonesMichael R. PeelDepartment of Chemjstry, Wayne State University, Detroit, Michigan 48202, USA
Johnson Carl R.Department of Chemjstry, Wayne State University, Detroit, Michigan 48202, USA
Chapter 22. Dimerization and polymerization of enones in the fluid and solid statesCharis R. TheocharisDepartment of Chemistry, Brunei University, Uxbridge, Middlesex UB8 3PH, UK
The Chemistry of the Metal—Carbon Bond, Volume 5 (1989) (See Volume 1 in 1983, Volume 2in 1985, Volume 3 in 1985, Volume 4 in 1987)
Edited by Frank R. Hartley
Chapter 1. The application of sonochemistry in the formation and reactions of metal—carbonbondsD. BremnerDepartment of Molecular and Life Sciences, Dundee Institute of Technology, Bell Street, Dundee DD11HG, Scotland, UK
Chapter 2. The photochemistry of organometallic compoundsConor LongSchool of Chemical Sciences, National Institute for Higher Education, Dublin 9, Ireland
Chapter 3. Phase-transfer catalysis in organometallic chemistryJean-Francois PetrignaniIPSOI, CNRS UA 126, Faculte des Sciences de Saint Jerome, Universite d’Aix Marseille, Av. dep’escadrille Normandie Niemen, 13397 Marseille, France
Chapter 4. Enantioselective syntheses with optically active transition metal catalystsH. BrunnerInstitut fur Anorganische Chemie, Universitat Regensburg, Universitatsstrasse 31, D-8400 Regensburg,FRG
Chapter 5. Organometallic oxidation catalystsGabor SpeierInstitute of Organic Chemistry, Veszprem University of Chemical Engineering, Veszprem 8200, Hungary
80
Chapter 6. Olefin metathesisW. James FeastDepartment of Chemistry, University of Durham, South Road, Durham DH1 3LE, UK
Vernon C. GibsonDepartment of Chemistry, University of Durham, South Road, Durham DH1 3LE, UK
Chapter 7. The use of transition metal clusters in organic synthesisG. Suss-FinkAachen University of Technology, Institute of Inorganic Chemistry, Templergraben 55, D-5100 Aachen,FRG
F. NeumannAachen University of Technology, Institute of Inorganic Chemistry, Templergraben 55, D-5100 Aachen,FRG
Chapter 8. Lanthanide reagents in organic synthesisGary A. MolanderDepartment of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309-0215, USA
Chapter 9. The use of organoantimony and organobismuth compounds in organic synthesisLeon D. FreedmanDepartment of Chemistry, North Carolina State University, Raleigh, North Carolina 27695-8204, USA
George O. DoakDepartment of Chemistry, North Carolina State University, Raleigh, North Carolina 27695-8204, USA
Chapter 10. Biological and environmental methylation of metalsPeter J. CraigSchool of Chemistry, Leicester Polytechnic, P.O. Box 143, Leicester LE1 9BH, UK
Chapter 11. Bioorganotin compoundsKieran C. MolloySchool of Chemistry, University of Bath, Claverton Down, Bath BA2 7AY, UK
The Chemistry of Organic Silicon Compounds, Volume 1, Part 1 (1989)(See Volume 2 in 1998)
Edited by Saul Patai and Zvi Rappoport
Chapter 1. Historical Overview and Comparison of Silicon with CarbonJoyce Y. CoreyUniversity of Missouri-St. Louis, St. Louis, MO 63121-4499, USA
Chapter 2. Theoretical Aspects of Organosilicon CompoundsYitzhak ApeloigDepartment of Chemistry, Technion—Israel Institute of Technology, Haifa 32000, Israel
Chapter 3. Structural Chemistry of Organic Silicon CompoundsW. S. SheldrickFachbereich Chemie der Universitat Kaiserslautern, Erwin-Schrodinger-Straße , D-6750 Kaiserslautern,Federal Republic of Germany
81
Chapter 4. Dynamic Stereochemistry at SiliconRobert J. P. CorriuInstitut de Chimie Fine, Heterochimie et Amino-Acides, Unite Associee CNRS U.A. n◦ 1097, Universite desSciences et Techniques du Languedoc, 34060 Montpellier Cedex, France
Christian GuerinInstitut de Chimie Fine, Heterochimie et Amino-Acides, Unite Associee CNRS U.A. n◦ 1097, Universite desSciences et Techniques du Languedoc, 34060 Montpellier Cedex, France
Joel J. E. MoreauInstitut de Chimie Fine, Heterochimie et Amino-Acides, Unite Associee CNRS U.A. n◦ 1097, Universite desSciences et Techniques du Languedoc, 34060 Montpellier Cedex, France
Chapter 5. ThermochemistryR. WalshDepartment of Chemistry, University of Reading, Whiteknights, PO Box 224, Reading RG6 2AD, UK
Chapter 6. Analysis of Organosilicon CompoundsT. R. Crompton‘Beechcroft’, Wittingham Lane, Goosnargh, Preston, Lancashire, UK
Chapter 7. Positive and Negative Ion Chemistry of Silicon-Containing Molecules in the Gas PhaseHelmut SchwarzInstitut fur Organische Chemie der Technischen Universitat Berlin, Straße des 17. Juni 135, D-1000 Berlin12, FRG
Chapter 8. NMR Spectroscopy of Organosilicon CompoundsElizabeth A. WilliamsGeneral Electric Co., Corporate Research and Development, PO Box 8, Schenectady, New York 12301,USA
Chapter 9. Photoelectron Spectra of Silicon CompoundsH. BockInstitute of Inorganic Chemistry, Johann Wolfgang Goethe University, Niederurseler Hang, D-6000Frankfurt (M) 50, West Germany
B. SoloukiInstitute of Inorganic Chemistry, Johann Wolfgang Goethe University, Niederurseler Hang, D-6000Frankfurt (M) 50, West Germany
Chapter 10. General Synthetic Pathways to Organosilicon CompoundsLeonhard BirkoferInstitute of Organic Chemistry, University of Dusseldorf, D-4000 Dusseldorf 1, West Germany
Oskar StuhlInstitute of Organic Chemistry, University of Dusseldorf, D-4000 Dusseldorf 1, West Germany
Chapter 11. Recent Synthetic Applications of OrganosilanesGerald L. LarsonPetrarch Systems, Bartram Road, Bristol, PA 19007, USA
Chapter 12. Acidity, Basicity and Complex Formation of Organosilicon CompoundsAlan R. BassindalePORCG, Department of Chemistry, The Open University, Milton Keynes, MK7 6AA, England
82
Peter G. TaylorPORCG, Department of Chemistry, The Open University, Milton Keynes, MK7 6AA, England
Chapter 13. Reaction Mechanisms of Nucleophilic Attack at SiliconAlan R. BassindalePORCG, Department of Chemistry, The Open University, Milton Keynes MK7 6AA, England
Peter G. TaylorPORCG, Department of Chemistry, The Open University, Milton Keynes MK7 6AA, England
Chapter 14. Activating and Directive Effects of SiliconAlan R. BassindalePORCG, Department of Chemistry, The Open University, Milton Keynes, MK7 6AA, England
Peter G. TaylorPORCG, Department of Chemistry, The Open University, Milton Keynes, MK7 6AA, England
Chapter 15. The Photochemistry of Organosilicon CompoundsA. G. BrookLash Miller Chemical Laboratories, University of Toronto, Toronto, M5S 1A1, Canada
Chapter 16. Trivalent Silyl IonsJoseph B. LambertDepartment of Chemistry, Northwestern University, Evanston, Illinois 60208, USA
W. J. Schulz Jr.Department of Chemistry, Northwestern University, Evanston, Illinois 60208, USA
Chapter 17. Multiple Bonds to SiliconGerhard RaabeLehr- und Forschungsgebiet Theoretische Chemie der Rheinisch–Westfalischen Technischen HochschuleAachen, D-5100 Aachen, Federal Republic of Germany
Josef MichlCenter for Structure and Reactivity, Department of Chemistry, The University of Texas at Austin, Austin,Texas 78712-1167, USA
Chapter 18. Bioorganosilicon ChemistryReinhold TackeInstitut fur Anorganische und Analytische Chemie, Technische Universitat Braunschweig, D-3300Braunschweig, FRG, Germany
Haryanto LinohInstitut fur Anorganische und Analytische Chemie, Technische Universitat Braunschweig, D-3300Braunschweig, FRG, Germany
Chapter 19. PolysilanesRobert WestDepartment of Chemistry, University of Wisconsin, Madison, WI 53706, USA
Chapter 20. Hypervalent Silicon CompoundsRobert J. P. CorriuInstitut de Chimie Fine, Heterochimie et Amino-Acides, Unite Associee C.N.R.S. U.A. No. 1097, Universitedes Sciences et Techniques du Languedoc, 34060 Montpellier Cedex, France
J. Colin YoungEdward Davies Chemical Laboratories, The University College of Wales, Aberystwyth SY23 1NE, UK
83
Chapter 21. Siloxane Polymers and CopolymersT. C. KendrickDow Corning Ltd, Barry, S. Glamorgan, CF6 7YL, UK
B. ParbhooDow Corning Ltd, Barry, S. Glamorgan, CF6 7YL, UK
J. W. WhiteDow Corning Ltd, Barry, S. Glamorgan, CF6 7YL, UK
Chapter 22. Organosilicon Derivatives of Phosphorus, Arsenic, Antimony and BismuthD. A. (‘Fred’) ArmitageDepartment of Chemistry, King’s College London (KQC), Strand, London WC2R 2LS, England
Chapter 23. Chemistry of Compounds with Silicon–Sulphur, Silicon–Selenium andSilicon–Tellurium BondsD. A. (‘Fred’) ArmitageDepartment of Chemistry, King’s College London (KQC), Strand, London WC2R 2LS, England
Chapter 24. Transition-Metal Silyl DerivativesT. Don TilleyDepartment of Chemistry, D-006, University of California at San Diego, La Jolla, California 92093, USA
Chapter 25. The Hydrosilylation ReactionIwao OjimaDepartment of Chemistry, State University of New York at Stony Brook, Stony Brook, NY 11794-3400, USA
Crown Ethers and Analogs (1989)Edited by Saul Patai and Zvi Rappoport
Chapter 1. Synthesis of crown ethers and analoguesDale A. LaidlerNew Business Planning Group, ICI plc, Runcorn, England and University of Sheffield, England
J. Fraser StoddartNew Business Planning Group, ICI plc, Runcorn, England and University of Sheffield, England
Chapter 2. Organic transformations mediated by macrocyclic multidentate ligandsCharles L. LiottaSchool of Chemistry, Georgia Institute of Technology, Atlanta, Georgia 30332, USA
Chapter 3. Modern aspects of host–guest chemistry: molecular modeling and conformationallyrestricted hostsJohn L. TonerExploratory Sciences Division, Life Sciences Research Laboratories Eastman Kodak Company, Rochester,New York 14650, USA
Chapter 4. Crown ethers—complexes and selectivityFritz VogtleInstitut fur Organische Chemie und Biochemie der Universitat, Gerhard-Domagk Strasse 1, D-5300Bonn-1, FRG
84
Edwin WeberInstitut fur Organische Chemie und Biochemie der Universitat, Gerhard-Domagk Strasse 1, D-5300Bonn-1, FRG
Chapter 5. New developments in crown ether chemistry: Lariat, spherand and second-spherecomplexesEdwin WeberInstitut fur Organische Chemie und Biochemie der Universitat, Gerhard-Domagk-Strasse 1, D-5300Bonn-1, FRG
Chapter 6. Geometry of the ether, sulphide and hydroxyl groups and structural chemistry ofmacrocyclic and non-cyclic polyether compoundsIsrael GoldbergSchool of Chemistry, Tel Aviv University, Ramat Aviv, 69978 Tel Aviv, Israel
Chapter 7. Structural chemistry of crown ethersIsrael GoldbergSchool of Chemistry, Sackler Faculty of Exact Sciences, Tel Aviv University, Ramat Aviv, 69978 Tel Aviv,Israel
Chapter 8. Complexation of aryldiazonium ions by polyethersRichard A. BartschDepartment of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409, USA
Chapter 9. Appendix to complexation of aryldiazonium ions by polyethersRichard A. BartschDepartment of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409, USA
Nitrones, Nitronates and Nitroxides (1989)Edited by Saul Patai and Zvi Rappoport
Chapter 1. Nitronic acids and estersArnold T. NielsenMichelson Laboratory, Naval Weapons Center, China Lake, California
Chapter 2. Nitrones and nitronic acid derivatives: Their structure and their roles in synthesisEli BreuerDepartment of Pharmaceutical Chemistry, The School of Pharmacy, The Hebrew University of Jerusalem,Jerusalem, Israel
Chapter 3. Nitrones and nitronic acid derivatives: An updateEli BreuerDepartment of Pharmaceutical Chemistry, The School of Pharmacy, The Hebrew University of Jerusalem,Jerusalem, Israel
Chapter 4. NitroxidesHans Gunter AurichFachbereich Chemie, Philipps-Universitat Marburg, Marburg, Federal Republic of Germany
Chapter 5. Appendix to ‘Nitroxides’Hans Gunter AurichFachbereich Chemie, Philipps-Universitat Marburg, Marburg, Federal Republic of Germany
85
The Chemistry of Enols (1990)Edited by Zvi Rappoport
Chapter 1. Theoretical calculationsYitzhak ApeloigDepartment of Chemistry, Technion—Israel Institute of Technology, Haifa 32000, Israel
Chapter 2. Thermodynamics of enolsJ. Peter GuthrieUniversity of Western Ontario, London, Ontario, Canada
Chapter 3. The chemistry of ionized enols in the gas phaseFrantisek TurecekDepartment of Chemistry, Baker Laboratory, Cornell University, Ithaca, New York, USA
Chapter 4. NMR, IR, conformation and hydrogen bondingB. FlorisDipartimento di Chimica, Universita di Roma ‘La Sapienza’, I-00185 Rome, Italy
Chapter 5. The generation of unstable enolsBrian CaponChemistry Department, University of Hong Kong, Pokfulam Road, Hong Kong
Chapter 6. Keto–enol equilibrium constantsJean ToullecInstitut de Topologie et de Dynamique des Systemes de l’Universite Paris 7, associe au CNRS, 1, rue Guyde la Brosse, 75005 Paris, France
Chapter 7. Kinetics and mechanism of enolization and ketonizationJames R. KeeffeDepartment of Chemistry and Biochemistry, San Francisco State University, San Francisco, CA 94132,USA
A. Jerry KresgeDepartment of Chemistry, University of Toronto, Toronto, Ontario M5S 1A1, Canada
Chapter 8. Isolable and relatively stable simple enolsHarold HartDepartment of Chemistry, Michigan State University, East Lansing, Michigan 48824, USA
Zvi RappoportDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel
Silvio E.BialiDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel
Chapter 9. Photochemical reactions involving enolsAlan C. WeedonPhotochemistry Unit, Department of Chemistry, University of Western Ontario, London, Ontario, Canada
Chapter 10. Enols of carboxylic acids and estersA. F. HegartyChemistry Department, University College Dublin, Belfield, Dublin 4, Ireland
P. O’NeillChemistry Department, University College Dublin, Belfield, Dublin 4, Ireland
86
Chapter 11. The biochemistry of enolsJohn P. RichardDepartment of Chemistry, The University of Kentucky, Lexington, Kentucky 40506 0055, USA
Chapter 12. Organometallic chemistry of enolsDavid MilsteinDepartment of Organic Chemistry, The Weizmann Institute of Science, Rehovot 76100, Israel
Chapter 13. Structural chemistryGastone GilliDipartimento di Chimica e Centro di Strutturistica Diffrattometrica, Universita’ di Ferrara, 44100Ferrara, Italy
Valerio BertolasiDipartimento di Chimica e Centro di Strutturistica Diffrattometrica, Universita’ di Ferrara, 44100Ferrara, Italy
The Chemistry of Organophosphorus Compounds, Volume 1 (1990) (See Volume 2 in 1992,Volume 3 in 1993, Volume 4 in 1996)
Edited by Frank R. Hartley
Chapter 1. IntroductionF. R. HartleyCranfield Institute of Technology, Cranfield, Bedford, MK43 OAL, UK
Chapter 2. Structure and bonding in organophosphorus(III) compoundsD. G. GilheanyDepartment of Chemistry, St Patrick’s College, Maynooth, Co. Kildare, Ireland
Chapter 3. Optically active phosphines: preparation, uses and chiroptical propertiesH. B. KaganLaboratoire de Synthese Asymetrique, UA CNRS 255, Universite Paris-Sud, 91405 Orsay, France
M. SasakiLaboratoire de Synthese Asymetrique, UA CNRS 255, Universite Paris-Sud, 91405 Orsay, France
Chapter 4. Electrochemistry of organophosphorus(III) compoundsK. S. V. SanthanamChemical Physics Group, Tata Institute of Fundamental Research, Colaba, Bombay 400005, India
Chapter 5. Thermochemistry of phosphorus(III) compoundsG. PilcherDepartment of Chemistry, University of Manchester, Manchester M13 9PL, UK
Chapter 6. ESR spectra of free radicals derived from phosphinesP. TordoUniversite de Provence, CNRS UA 126-Boite 521, Av. Normandie-Niemen, 13397 Marseille, France
Chapter 7. Preparation of phosphinesD. G. GilheanyDepartment of Chemistry, St Patricks College, Maynooth, Co. Kildare, Ireland
87
C. M. MitchellDepartment of Chemistry, St Patricks College, Maynooth, Co. Kildare, Ireland
Chapter 8. The preparation and reactivity of bi- and poly-dentate phosphines with P—Cn—PbondingO. StelzerFachbereich 9, Anorganische Chemie, Bergische Universitat-GH Wuppertal, Gauss-Strasse 20, D-5600Wuppertal 1, FRG
K.-P. LanghansFachbereich 9, Anorganische Chemie, Bergische Universitat-GH Wuppertal, Gauss-Strasse 20, D-5600Wuppertal 1, FRG
Chapter 9. Chemistry and ligating properties of phospha-alkynes and their derivativesM. J. MaahCentre for Foundation Studies in Science, University of Malaya, 59100 Kuala Lumpur, Malaysia
Chapter 10. Cyclic phosphinesL. D. QuinDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts, USA
A. N. HughesDepartment of Chemistry, Lakehead University, Thunder Bay, Ontario, Canada
Chapter 11. Nucleophilic reactions of phosphinesH. R. HudsonDepartment of Applied Chemistry and Life Sciences, Polytechnic of North London, Holloway Road,London N7 8 DB, UK
Chapter 12. Acid–base and hydrogen-bonding properties of phosphinesH. R. HudsonDepartment of Applied Chemistry and Life Sciences, Polytechnic of North London, Holloway Road,London N7 8 DB, UK
Chapter 13. Photochemistry of organophosphorus(III) compoundsM. DankowskiDegussa AG, Geschaftsbereich Anorganische Chemieprodukte D-6000 Frankfurt, FRG
Chapter 14. Free-radical reactions of organophosphorus(III)Wesley G. BentrudeDepartment of Chemistry, University of Utah, Salt Lake City, Utah 84112, USA
Chapter 15. Phosphine complexes of transition metalsW. LevasonDepartment of Chemistry, University of Southampton, Southampton S09 5 NH, UK
Chapter 16. Biochemistry of phosphinesN. R. PriceADAS Slough Laboratory, London Road, Slough SL3 7HJ, UK
J. ChambersADAS Slough Laboratory, London Road, Slough SL3 7HJ, UK
88
The Chemistry of Sulphinic Acids, Esters and Derivatives (1990)Edited by Saul Patai
Chapter 1. Sulphinic acids and carboxylic acids—a comparisonCharles J. M. StirlingDepartment of Chemistry, University College of North Wales, Bangor, Gwynedd LL57 2UW, UK
Chapter 2. General and theoreticalHarold BaschDepartment of Chemistry, Bar-Ilan University, Ramat Gan 52100, Israel
Chapter 3. Sulfinic acids and their derivatives. Stereochemistry and chiroptical propertiesAbraham NudelmanDepartment of Chemistry, Bar-Ilan University, Ramat Gan 52100, Israel
Chapter 4. Analytical methodsM. R. F. AshworthOrganische und Instrumentelle Analytik, Universitat des Saarlandes, D-6600 Saarbrucken, FRG
Chapter 5. Mass spectra of sulfinic acids, esters and derivativesKalevi PihlajaDepartment of Chemistry, University of Turku, SF-20500 Turku, Finland
Chapter 6. The NMR and ESR spectra of sulphinic acids and their derivativesAlan R. BassindalePOCRG, Department of Chemistry, The Open University, Walton Hall, Milton Keynes MK7 6AA, England
James N. IleyPOCRG, Department of Chemistry, The Open University, Walton Hall, Milton Keynes MK7 6AA, England
Chapter 7. Syntheses of sulfinic acidsUri ZollerDivision of Chemical Studies, Haifa University—Oranim, P.O. Kiryat Tivon 36910, Israel
Chapter 8. Syntheses of sulfinic estersUri ZollerDivision of Chemical Studies, Haifa University—Oranim, P.O. Kiryat Tivon 36910, Israel
Chapter 9. Cyclic sulphinic acid derivatives (sultines and sulphinamides)Donald C. DittmerDepartment of Chemistry, Syracuse University, Syracuse, New York 13244-1200, USA
Michael D. HoeyDepartment of Chemistry, Syracuse University, Syracuse, New York 13244-1200, USA
Chapter 10. Acidity, hydrogen bonding and complexationHisashi FujiharaDepartment of Chemistry, University of Tsukuba, Tsukuba, Ibaraki 305, Japan
Naomichi FurukawaDepartment of Chemistry, University of Tsukuba, Tsukuba, Ibaraki 305, Japan
Chapter 11. RearrangementsSamuel BravermanDepartment of Chemistry, Bar-Ilan University, Ramat Gan 59100, Israel
89
Chapter 12. Sulphinic acids and esters in synthesisJozef DrabowiczCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363, Lodz, Poland
Piotr KielbasinskiCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363, Lodz, Poland
Marian MikolajczykCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363, Lodz, Poland
Chapter 13. Photochemistry of sulphinic acid derivativesGiuseppe CapozziCentro C. N. R. ‘Chimica e Struttura dei Composti Eterociclici, c/o Dipartimento di Chimica Organica,Universita’ di Firenze, 50121 Firenze, Italy
Piero Sarti-FantoniCentro C. N. R. ‘Chimica e Struttura dei Composti Eterociclici, c/o Dipartimento di Chimica Organica,Universita’ di Firenze, 50121 Firenze, Italy
Chapter 14. The oxidation and reduction of sulphinic acids and their derivativesJeffrey HoyleChemistry-Soils Department, Nova Scotia Agricultural College, P.O. Box 550, Truro, Nova Scotia, CanadaB2N5E3
Chapter 15. Synthesis and uses of isotopically labelled sulfinic acid derivativesShigeru OaeDepartment of Chemistry, Okayama University of Science, Ridai-cho 1-1, Okayama, 700 Japan
Hideo TogoDepartment of Chemistry, Faculty of Science, Chiba University, Yayoi-cho, Chiba City, 260 Japan
Chapter 16. Thermochemistry and thermolysis of sulphinic acid derivativesBogdan BujnickiCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363 Lodz, Poland
Marian MikolajczykCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363 Lodz, Poland
Jan OmelanczukCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363 Lodz, Poland
Chapter 17. Electronic effects of SOOH and related groupsJohn ShorterDepartment of Chemistry, The University, Hull, HU6 7RX, UK
Chapter 18. Thiosulphinic acids and estersToshikazu TakataResearch Laboratory of Resources Utilization, Tokyo Institute of Technology, Nagatsuta-cho Midori-ku,Yokohama 227, Japan
90
Takeshi EndoResearch Laboratory of Resources Utilization, Tokyo Institute of Technology, Nagatsuta-cho Midori-ku,Yokohama 227, Japan
Chapter 19. Sulphinyl chlorides and sulphinic anhydridesJ. G. TillettDepartment of Chemistry and Biological Chemistry, University of Essex, Colchester, CO4 3SQ, UK
Chapter 20. SulphinamidesJ. G. TillettDepartment of Chemistry and Biological Chemistry, University of Essex, Colchester, CO4 3SQ, UK
Chapter 21. Mechanism of nucleophilic displacement reactions of sulfinic acid derivativesTadashi OkuyamaFaculty of Engineering Science, Osaka University, Toyonaka, Osaka 560, Japan
Chapter 22. Sulfinate ions as nucleophilesTadashi OkuyamaFaculty of Engineering Science, Osaka University, Toyonaka, Osaka 560, Japan
Chapter 23. Biological activity of sulfinic acid derivativesAsher KalirDepartment of Physiology and Pharmacology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv69978, Israel
Henry H. KalirDepartment of Neurobiology, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY10029, USA
The Chemistry of Sulphenic Acids and Derivatives (1990)Edited by Saul Patai
Chapter 1. Structural chemistryG. C. BarrettOxford Polytechnic, Oxford OX3 OBP, UK
Chapter 2. Stereochemistry and chiroptical propertiesDaniel KostDepartment of Chemistry, Ben-Gurion University of the Negev, Beer Sheva 84105, Israel
Morton RabanDepartment of Chemistry, Wayne State University, Detroit, Michigan 48202, USA
Chapter 3. Analytical aspects of sulfenic acids and their functional derivativesJacob ZabickyThe Institutes for Applied Research, Ben-Gurion University of the Negev, Beer Sheva, Israel
Chapter 4. NMR and ESR of sulphenic acids and their derivativesAlan R. BassindalePhysical Organic Chemistry Research Group, Chemistry Department, The Open University, Milton KeynesMK7 6AA, UK
91
Jim IleyPhysical Organic Chemistry Research Group, Chemistry Department, The Open University, Milton KeynesMK7 6AA, UK
Chapter 5. Synthesis of sulphenic acids and estersJozef DrabowiczPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, 90-363 Lodz, Sienkiewicza 112, Poland
Piotr LyzwaPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, 90-363 Lodz, Sienkiewicza 112, Poland
Marian MikolajczykPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, 90-363 Lodz, Sienkiewicza 112, Poland
Chapter 6. Synthesis of sulphenyl halides and sulphenamidesJozef DrabowiczCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363 Lodz, Poland
Piotr KielbasinskiCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363 Lodz, Poland
Marian MikolajczykCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363 Lodz, Poland
Chapter 7. Acidity, hydrogen bonding and complex formationPaolo De MariaDepartment of Organic Chemistry, University of Palermo, via Archirafi, 20, 90123—Palermo, Italy
Chapter 8. Rearrangements involving sulfenic acids and their derivativesSamuel BravermanDepartment of Chemistry, Bar-llan University, Ramat Gan 52100, Israel
Chapter 9. Chemistry of sulphenic acids and estersD. R. HoggDepartment of Chemistry, University of Aberdeen. Meston Walk, Old Aberdeen AB9 2UE, Scotland
Chapter 10. Chemistry of sulphenyl halides and sulphenamidesG. CapozziCentro Chimica e Struttura dei Composti Eterociclici, CNR, Dipartimento di Chimica Organica ‘UgoShift’, I-50121, Firenze, Italy
G. ModenaCentro Meccanismi di Reazioni Organiche, CNR, Dipartimento di Chimica Organica, via Marzolo 1,I-35131, Padova, Italy
L. PasquatoCentro Meccanismi di Reazioni Organiche, CNR, Dipartimento di Chimica Organica, via Marzolo 1,I-35131, Padova, Italy
92
Chapter 11. Photochemistry and radiation chemistryWilliam M. HorspoolDepartment of Chemistry, University of Dundee, Dundee DD1 4HN, Scotland
Chapter 12. Free radical chemistry of sulfenic acids and their derivativesC. ChatgilialogluIstituto dei composti del carbonio contenenti eteroatomi e loro applicazioni, C.N.R., 40064 Ozzano Emilia(Bologna), Italy
Chapter 13. Electrochemistry of sulfenic acids and their derivativesH. SayoKobe-Gakuin University, Nishi-Ku, Kobe, 673 Japan
Chapter 14. Syntheses and uses of isotopically labelled sulphenic acid derivativesMieczyslaw ZielinskiIsotope Laboratory, Faculty of Chemistry, Jagiellonian University, Cracow, Poland
Marianna KanskaDepartment of Chemistry, University of Warsaw, Warsaw, Poland
Chapter 15. Directing and activating effects of chalcogen substituerasMarvin ChartonChemistry Department, School of Liberal Arts and Sciences, Pratt Institute, Brooklyn, NY 11205, USA
Chapter 16. Biochemistry and metabolic pathways of sulfenic acids and their derivativesLeon A. G. M. Van Den BroekOrganon International BV, P.O. Box 20, 5340 BH Oss, The Netherlands
Leon P. C. DelbressineOrganon International BV, P.O. Box 20, 5340 BH Oss, The Netherlands
Harry C. J. OttenheijmOrganon International BV, P.O. Box 20, 5340 BH Oss, The Netherlands
Chapter 17. SulfeniminesPeter K. ClausInstitute of Organic Chemistry, University of Vienna, Austria
Chapter 18. Mechanistic aspects of nucleophilic substitutions of sulfenic acid derivativesTadashi OkuyamaFaculty of Engineering Science, Osaka University, Toyonaka, Osaka 560, Japan
Cyclopropane Derived Reactive Intermediates (1990)Edited by Saul Patai and Zvi Rappoport
Chapter 1. Cyclopropyl radicals, anion radicals and anions
Chapter 2. Appendix to ‘Cyclopropyl radicals, anion radicals and anions’
Chapter 3. Cyclopropyl cations
Chapter 4. Cyclopropyl carbenoids
Chapter 5. Cyclopropane cation radicals
93
The Chemistry of Amidines and Imidates, Volume 2 (1991) (See Volume 1 in 1975)
Edited by Saul Patai and Zvi Rappoport
Chapter 1. General and theoretical aspects of amidines and related compoundsGunter HafelingerInstitute of Organic Chemistry, University of Tubingen, Auf der Morgenstelle 18, 7400 Tubingen, Germany
Frank K. H. KuskeInstitute of Organic Chemistry, University of Tubingen, Auf der Morgenstelle 18, 7400 Tubingen, Germany
Chapter 2. Structural chemistry of amidines and related systemsTadeusz Marek KrygowskiThe Hebrew University, Jerusalem
Krzysztof WozniakThe Hebrew University, Jerusalem
Chapter 3. Stereochemical aspects of amidjnes, imidates and related compoundsCharles L. PerrinDepartment of Chemistry D-006, University of California San Diego, La Jolla, California 92093-0506,USA
Chapter 4. Detection and determination of imidic acid derivativesIrena Busko-OszczapowiczBiotechnology Research and Development Center, Warsaw, Poland
Janusz OszczapowiczDepartment of Chemistry, University of Warsaw, Warsaw, Poland
Chapter 5. Mass spectra of amidines and related compoundsSimonetta FornariniDipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, Universita di Roma‘La Sapienza’, I-00185 Rome, Italy
Chapter 6. Thermochemistry of amidines and related compoundsKalevi PihlajaDepartment of Chemistry, University of Turku, SF-20500 Turku, Finland
Chapter 7. Recent advances in the synthesis of amidinesGerhard V. BoydDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem, Israel
Chapter 8. Reactions and synthetic uses of amidinesGerhard V. BoydDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem, Israel
Chapter 9. Imidates including cyclic imidatesDouglas G. NeilsonChemistry Department, The University, Dundee, Scotland, UK
Chapter 10. Synthesis and chemistry of guanidine derivativesYohsuke YamamotoDepartment of Chemistry, Faculty of Science, Hiroshima University, Hiroshima, Japan
Satoshi KojimaDepartment of Chemistry, Faculty of Science, Hiroshima University, Hiroshima, Japan
94
Chapter 11. Rearrangements in amidines and related compoundsVladimir I. MinkinInstitute of Physical and Organic Chemistry, Rostov University, 344711 Rostov on Don, USSR
Igor E. MikhailovInstitute of Physical and Organic Chemistry, Rostov University, 344711 Rostov on Don, USSR
Chapter 12. Basicity, H-bonding, tautomerism and complex formation of imidic acid derivativesJanusz OszczapowiczDepartment of Chemistry, University of Warsaw, Warsaw, Poland
Chapter 13. Electronic effects of amidino, guanidino and related groupsJohn ShorterDepartment of Chemistry, The University, Hull HU6 7RX, UK
Chapter 14. Radiation chemistry of amidinesZeev B. AlfassiDepartment of Nuclear Engineering, Ben-Gurion University of the Negev, 84105 Beer Sheva, Israel
Chapter 15. Catalysis by amidinesPer AhlbergDepartment of Organic Chemistry, University of Goteborg, S-41296 Goteborg, Sweden
Lena SwahnDepartment of Organic Chemistry, University of Goteborg, S-41296 Goteborg, Sweden
Chapter 16. Electrochemistry of amidinesJan S. JaworskiDepartment of Chemistry, The University of Warsaw, 02-093 Warszawa, Poland
Marek K. KalinowskiDepartment of Chemistry, The University of Warsaw, 02-093 Warszawa, Poland
The Chemistry of Sulphonic Acids, Esters and their Derivatives (1991)Edited by Saul Patai and Zvi Rappoport
Chapter 1. General and TheoreticalHarold BaschDepartment of Chemistry, Bar-Ilan University, Ramat Gan 52100, Israel
Tova HozDepartment of Chemistry, Bar-Ilan University, Ramat Gan 52100, Israel
Chapter 2. Stereochemistry, Conformation, and Chiroptical Properties of Sulfonic Acids andDerivativesKenneth K. AndersenDepartment of Chemistry, University of New Hampshire, Durham, NH 03824, USA
Chapter 3. Mass Spectrometry of Sulfonic Acids and their DerivativesSimonetta FornariniDipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, Universita degliStudi di Roma ‘La Sapienza’, Piazzale Aldo Moro 5, I-00185 Rome, Italy
95
Chapter 4. Ultraviolet Photoelectron Spectroscopy of Organic Sulfur CompoundsJ. Barrie PeelDepartment of Chemistry and Research Centre for Electron Spectroscopy, La Trobe University, Bundoora,Victoria 3083, Australia
Chapter 5. The NMR and ESR Spectra of Sulphonic Acids and their DerivativesAlan R. BassindalePOCRG, Department of Chemistry, The Open University, Walton Hall, Milton Keynes, MK7 6AA, UK
James N. IleyPOCRG, Department of Chemistry, The Open University, Walton Hall, Milton Keynes, MK7 6AA, UK
Chapter 6. AcidityJ. F. KingDepartment of Chemistry, The University of Western Ontario, London, Ontario, Canada N6A 5B7, Canada
Chapter 7. Acidity, Hydrogen Bonding and Metal Complexation of Sulfonic Acids and DerivativesNaomichi FurukawaDepartment of Chemistry, University of Tsukuba, Tsukuba, Ibaraki 305, Japan
Hisashi FujiharaDepartment of Chemistry, University of Tsukuba, Tsukuba, Ibaraki 305, Japan
Chapter 8. Thermochemistry of Sulphonic Acids and their DerivativesJoel F. LiebmanDepartment of Chemistry and Biochemistry, The University of Maryland, Baltimore County Campus,Baltimore, Maryland 21228, USA
Chapter 9. Analytical MethodsM. R. F. AshworthFachrichtung 15.3, Organische und Instrumentelle Analytik, Universitat des Saarlandes, 6600Saarbrucken, Germany
Chapter 10. Preparation of Sulphonic Acids, Esters, Amides and HalidesJeffrey HoyleDepartment of Chemistry-Soils, Nova Scotia Agricultural College, P.O. Box 550, Truro, Nova Scotia,Canada B2N 5E3, Canada
Chapter 11. Sulfonic Acids, Esters, Amides and Halides as SynthonsKazuhiko TanakaDepartment of Chemistry, Faculty of Science, Kyoto University, Sakyo, Kyoto 606, Japan
Chapter 12. RearrangementsJim IleyPOCRG, Department of Chemistry, The Open University, Walton Hall, Milton Keynes, MK7 6AA, UK
Chapter 13. Photochemistry and Radiation ChemistryWilliam M. HorspoolDepartment of Chemistry, University of Dundee, Dundee, DDI 4HN, Scotland, UK
Chapter 14. Electrochemistry of Sulphonic Acids and their DerivativesJacques SimonetLaboratoire d’Electrochimie organique, CNRS, Universite de Rennes 1, France
96
Chapter 15. Syntheses and Uses of Isotopically Labelled Sulphonic Acid Derivatives and RelatedCompoundsMieczylaw ZielinskiIsotope Laboratory, Faculty of Chemistry, Jagiellonian University, 30-060 Krakow, Karasia 3, Poland
Marianna KanskaDepartment of Chemistry, University of Warsaw, Warsaw, Poland
Chapter 16. Directing and Activating Effects in Reactions Involving Sulphonic Acids andDerivativesT. William BentleyDepartment of Chemistry, University College of Swansea, Singleton Park, Swansea, SA2 8PP, Wales, UK
Chapter 17. SulfenesJ. F. KingDepartment of Chemistry, The University of Western Ontario, London, Ontario, Canada N6A 5B7, Canada
Rajendra RathoreDepartment of Chemistry, The University of Western Ontario, London, Ontario, Canada N6A 5B7, Canada
Chapter 18. Biological Activity of Sulfonic Acid DerivativesAsher KalirDepartment of Physiology and Pharmacology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv69978, Israel
Henry H. KalirDepartment of Neurology, Mount Sinai School of Medicine, The Mount Sinai Hospital, One Gustave L.Levy Place, New York, NY 10029-6574, USA
Chapter 19. Sultones and SultamsA. J. BuglassAnglia Higher Education College, East Road, Cambridge, CBI IPT, UK
J. G. TillettDepartment of Chemistry and Biological Chemistry, University of Essex, Wivenhoe Park, Colchester,Essex, CO4 3SQ, UK
Chapter 20. Polymers Containing SO3H and Related GroupsDavid M. VofsiThe Weizmann Institute of Science, Rehovot 76100, Israel
Chapter 21. Perfluoroalkanesulfonic Acids and their DerivativesWei-Yuan HuangShanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai200032, China
Qing-Yun ChenShanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai200032, China
Chapter 22. Sulphamic Acid and DerivativesG. A. BensonSchool of Science, Regional Technical College, Ballinode, Sligo, Ireland
William J. SpillaneDepartment of Chemistry, University College, Galway, Ireland
97
The Silicon–Heteroatom Bond (1991)Edited by Saul Patai and Zvi Rappoport
Chapter 1. Hypervalent silicon compoundsRobert J. P. CorriuInstitut de Chimie Fine, Heterochimie et Amino-Acides, Unite Associee C.N.R.S. U.A. No. 1097, Universitedes Sciences et Techniques du Languedoc, 34060 Montpellier Cedex, France
J. Colin YoungEdward Davies Chemical Laboratories, The University College of Wales, Aberystwyth SY23 1NE, UK
Chapter 2. Appendix to ‘Hypervalent silicon compounds’Robert J. P. CorriuURA CNRS 1097, Universite de Montpellier II, Sciences et Techniques du Languedoc, 34095 MontpellierCedex, France
J. Colin YoungURA CNRS 1097, Universite de Montpellier II, Sciences et Techniques du Languedoc, 34095 MontpellierCedex, France
Chapter 3. Siloxane polymers and copolymersT. C. KendrickDow Corning Ltd, Barry, S. Glamorgan, CF6 7YL, UK
B. ParbhooDow Corning Ltd, Barry, S. Glamorgan, CF6 7YL, UK
J. W. WhiteDow Corning Ltd, Barry, S. Glamorgan, CF6 7YL, UK
Chapter 4. Appendix to ‘Siloxane polymers and copolymers’T. C. KendrickDow Corning Ltd, Barry, S. Glamorgan, CF6 7YL, UK
B. ParbhooDow Corning Ltd, Barry, S. Glamorgan, CF6 7YL, UK
J. W. WhiteDow Corning Corporation, Midland, Michigan 48686-0994, USA
Chapter 5. Organosilicon derivatives of phosphorus, arsenic, antimony and bismuthD. A. (‘Fred’) ArmitageDepartment of Chemistry, King’s College London (KQC), Strand, London WC2R 2LS, England
Chapter 6. Appendix to ‘Organosilicon derivatives of phosphorus, arsenic, antimony and bismuth’D. A. (‘Fred’) ArmitageDepartment of Chemistry, King’s College, London (KQC), Strand, London WC2R 2LS, England
Chapter 7. Chemistry of compounds with silicon–sulphur, silicon–selenium and silicon–telluriumbondsD. A. (‘Fred’) ArmitageDepartment of Chemistry, King’s College London (KQC), Strand, London WC2R 2LS, England
Chapter 8. Appendix to ‘Chemistry of compounds with silicon–sulphur, silicon–selenium andsilicon–tellurium bonds’D. A. (‘Fred’) ArmitageDepartment of Chemistry, King’s College London (KQC), Strand, London WC2R 2LS, England
98
Chapter 9. Transition-metal silyl derivativesT. Don TilleyDepartment of Chemistry, D-006, University of California at San Diego, La Jolla, California 92093, USA
Chapter 10. Appendix to ‘Transition-metal silyl derivatives’T. Don TilleyDepartment of Chemistry, 0506, University of California, San Diego, 9500 Gilman Drive, La Jolla,California 92093-0506, USA
Chapter 11. Organosilicon nitrogen compoundsD. A. (‘Fred’) ArmitageDepartment of Chemistry, King’s College London (KQC), Strand, London WC2R 2LS, England
Chapter 12. Appendix to ‘Organosilicon nitrogen compounds’D. A. (‘Fred’) ArmitageDepartment of Chemistry, King’s College London (KQC), Strand, London WC2R 2LS, England
Synthesis of Carboxylic Acids, Esters and Their Derivatives (1991)Edited by Saul Patai and Zvi Rappoport
Chapter 1. The synthesis of carboxylic acids and esters and their derivatives
Chapter 2. Appendix to ‘The synthesis of carboxylic acids and esters and their derivatives’
The Chemistry of Acid Derivatives, Volume 2 (1992) (See Volume 1 in 1979)
Edited by Saul Patai
Chapter 1. General and theoreticalHarold BaschDepartment of Chemistry, Bar Ilan University, Ramat Gan 52100, Israel
Tova HozDepartment of Chemistry, Bar Ilan University, Ramat Gan 52100, Israel
Chapter 2. Thermochemistry of carboxylic acids and derivativesG. PilcherDepartment of Chemistry, University of Manchester, Manchester M13 9PL, UK
Chapter 3. Chiroptical properties of acid derivativesJan SandstromDivision of Organic Chemistry 3, Chemical Center, University of Lund, Sweden
Chapter 4. Mass spectrometry of carboxylic acid derivativesHelge EgsgaardCombustion Department, Risø National Laboratory, DK-4000 Roskilde, Denmark
Lars CarlsenNational Environmental Research Institute, Department of Environmental Chemistry, DK-4000 Roskilde,Denmark
99
Chapter 5. Nuclear magnetic resonance of acids and acid derivativesPoul Erik HansenInstitute for Life Sciences and Chemistry, Roskilde University, P.O. Box 260, DK-4000 Roskilde, Denmark
Chapter 6. ESR studies of organic free radicals from carboxylic acids and their derivativesMichael J. DaviesDepartment of Chemistry, University of York, Heslington, York Y01 5DD England
Bruce C. GilbertDepartment of Chemistry, University of York, Heslington, York Y01 5DD England
Adrian C. WhitwoodDepartment of Chemistry, University of York, Heslington, York Y01 5DD England
Chapter 7. Vibrational analysis of acid derivativesHerman O. DesseynLaboratory of Inorganic Chemistry, RUCA University of Antwerp. Groenenborgerlaan 171, 2020 Antwerp,Belgium
Chapter 8. Acid–base properties of carboxylic acids, esters and amidesRomuald I. ZalewskiDivision of General Chemistry, University of Economics, Poznan, Poland
Chapter 9. Syntheses and uses of isotopically labelled acid derivativesMieczyslaw ZielinskiIsotope Laboratory, Faculty of Chemistry, Jagiellonian University, Cracow, Poland
Marianna KanskaDepartment of Chemistry, University of Warsaw, Warsaw, Poland
Chapter 10. The chemistry of lactones and lactamsG. V. BoydDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel
Chapter 11. The synthetic uses of carboxylic acids and their derivativesJeffrey HoyleChemistry and Soil Science Department, Nova Scotia Agricultural College, Truro, Nova Scotia, Canada,B2N 5E3
Chapter 12. Vapour and gas-phase reactions of carboxylic acids and their derivativesKenneth A. HolbrookSchool of Chemistry, The University of Hull, Hull, HU6 7RX, North Humberside, UK
Chapter 13. Mechanistic aspects. Recent developments concerning mechanisms of acylation bycarboxylic acid derivativesD. P. N. SatchellDepartment of Chemistry, King’s College London, Strand, London WC2R 2LS, UK
R. S. SatchellDepartment of Chemistry, King’s College London, Strand, London WC2R 2LS, UK
Chapter 14. Thio derivativesS. KatoDepartment of Chemistry, Faculty of Engineering, Gifu University, Yanagido, Gifu 501-11, Japan
100
T. MuraiDepartment of Chemistry, Faculty of Engineering, Gifu University, Yanagido, Gifu 501-11, Japan
Chapter 15. Hydroxamic acidsJames W. MunsonThe Upjohn Company, Kalamazoo, Michigan 49001-0199, USA
Chapter 16. The chemistry of amidoximesDemetrios N. NicolaidesDepartment of Chemistry, Aristotelian University of Thessaloniki, Thessaloniki 54006, Greece
Evangelia A. VarellaDepartment of Chemistry, Aristotelian University of Thessaloniki, Thessaloniki 54006, Greece
Chapter 17. Preparation and chemistry of ortho acids, ortho esters and ortho amidesUlf PindurDepartment of Chemistry and Pharmacy, University of Mainz, D-6500 Mainz, Germany
Chapter 18. Recent developments concerning carboxyl groups in biochemistryAlan H. MehlerHoward University College of Medicine, Washington, DC, USA
Chapter 19. Pharmacology of acid derivativesAbraham DanonDepartment of Clinical Pharmacology. Ben Gurion University and Soroka Medical Center, Beer-Sheva,Israel
Zvi Ben-ZviDepartment of Clinical Pharmacology. Ben Gurion University and Soroka Medical Center, Beer-Sheva,Israel
Chapter 20. Photochemistry of esters, lactones and their thio analoguesHiroshi SuginomeOrganic Synthesis Division, Faculty of Engineering, Hokkaido University, Sapporo, 060, Japan
Chapter 21. Radiation chemistry of fatty and amino acidsS. V. JovanovicLaboratory 030, The Boris Kidric Institute of Nuclear Sciences, P.O. Box 522, 11001 Beograd, Yugoslavia
Lj. R. JosimovicLaboratory 030, The Boris Kidric Institute of Nuclear Sciences, P.O. Box 522, 11001 Beograd, Yugoslavia
Chapter 22. Electrochemistry of carboxylic acids: mechanistic aspects of Kolbe-type reactionsElisabet AhlbergDepartment of Inorganic Chemistry, Chalmers University of Technology and University of Goteborg,S-41296 Goteborg, Sweden
Chapter 23. RearrangementsMiguel A. MirandaDepartamento de Quımica-Instituto de Tecnologıa Quımica, Universidad Politecnica de Valencia-CSIC,Apartado 22012, 46071 Valencia, Spain
Hermenegildo GarcıaDepartamento de Quımica-Instituto de Tecnologıa Quımica, Universidad Politecnica de Valencia-CSIC,Apartado 22012, 46071 Valencia, Spain
101
Chapter 24. The application of lipases in organic synthesisGudmundur G. HaraldssonScience Institute, University of Iceland, Dunhaga 3, 107 Reykjavik, Iceland
Chapter 25. Diazoacetic acids and derivativesOleg M. NefedovN. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia
Evgenii A. ShapiroN. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia
Alexey B. DyatkinN. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia
Chapter 26. Anion radicals of aromatic carboxylic acids and their derivatives: structure andreactivityIsaak I. BilkisFaculty of Agriculture, The Hebrew University of Jerusalem, Rehovot 76100, Israel
The Chemistry of Alkanes and Cycloalkanes (1992)Edited by Saul Patai and Zvi Rappoport
Chapter 1. Atomic and Group Properties in the AlkanesRichard F. W. BaderDepartment of Chemistry, McMaster University, Hamilton, Ontario L8S 4MI, Canada
Chapter 2. Structural Chemistry of Alkanes—A Personal ViewEiji OsawaDepartment of Knowledge-Based Information Engineering, Toyohashi University of Technology,Tempaku-cho, Toyohashi 441, Japan
Chapter 3. Conformational Analysis of Acyclic and Alicyclic Saturated HydrocarbonsJ. E. AndersonChemistry Department, University College London, Gower Street, London WCIE 6BT, UK
Chapter 4. Chiroptical Properties of Alkanes and CycloalkanesJames H. BrewsterDepartment of Chemistry, Purdue University, West Lafayette, Indiana 47907-1393, USA Department ofChemistry, Purdue University, West Lafayette, Indiana 47907-3699, USA
Chapter 5. Enumeration, Topological Indices and Molecular Properties of AlkanesLowell H. HallDepartment of Chemistry, Eastern Nazarene College, Quincy, MA 02170, USA
Lemont B. KierDepartment of Medicinal Chemistry, Virginia Commonwealth University, Richmond, VA 23298, USA
Chapter 6. The Thermochemistry of Alkanes and CycloalkanesN. CohenThe Aerospace Corporation, P.O. Box 92957, Los Angeles, California 90009, USA
S. W. BensonLoker Hydrocarbon Research Institute, University of Southern California, Los Angeles, California 90089,USA
102
Chapter 7. The Analysis of Alkanes and CycloalkanesZeev AizenshtatDepartment of Organic Chemistry and Casali Institute of Applied Chemistry, The Hebrew University ofJerusalem, Jerusalem 91904, Israel
Chapter 8. NMR Spectroscopy of AlkanesStefan BergerDepartment of Chemistry, Philipps-Universitat Marburg, Hans-Meerwein-Strasse, D-3550 Marburg,Germany
Chapter 9. The Mass Spectra of AlkanesTino GaumannInstitute of Physical Chemistry, Federal School of Technology, CH-1015 Lausanne, Switzerland
Chapter 10. The Photoelectron Spectra of Saturated HydrocarbonsE. HeilbronnerGrutstrasse 10, CH-8704 Herrliberg, Switzerland
Chapter 11. Acidity and BasicityA. C. HopkinsonDepartment of Chemistry, York University, Downsview, Ontario M3J IP3, Canada
Chapter 12. Alkanes: Modern Synthetic MethodsGoverdhan MehtaSchool of Chemistry, University of Hyderabad, Central University PO, Hyderabad-500 134, IndiaJawaharlal Nehru Centre for Advanced Scientific Research, Indian Institute of Science Campus,Bangalore-560012, India
Rao H. Surya PrakashDepartment of Chemistry, Pondicherry University, Pondicherry-605 014, India
Chapter 13. Electrophilic Reactions on AlkanesGeorge A. OlahKatherine B. and Donald P. Loker Hydrocarbon Research Institute and Department of Chemistry,University of Southern California, Los Angeles, CA 90089-1661, USA
G. K. Surya PrakashKatherine B. and Donald P. Loker Hydrocarbon Research Institute and Department of Chemistry,University of Southern California, Los Angeles, CA 90089-1661, USA
Chapter 14. Organometallic Chemistry of Alkane ActivationRobert H. CrabtreeDepartment of Chemistry, Yale University, 225 Prospect Street, P.O. Box 6666, New Haven, Connecticut06511-8118, USA
Chapter 15. Rearrangements and Photochemical Reactions Involving Alkanes and CycloalkanesT. OppenlanderFachhochschule Furtwangen, Abteilung Villingen-Schwenningen, Fachbereich Verfahrenstechnik, D-7730VS-Schwenningen, Germany F. Hoffmann-La Roche AG, CH-4002, Basle, Switzerland
G. ZangDepartment of Organic Chemistry, University of Wurzburg, D-8700 Wurzburg, Germany
W. AdamDepartment of Organic Chemistry, University of Wurzburg, D-8700 Wurzburg, Germany
103
Chapter 16. Radiation Chemistry of Alkanes and CycloalkanesA. HummelInterfaculty Reactor Institute, Delft University of Technology, Mekelweg 15, 2629 JB Delft, TheNetherlands
Chapter 17. Electrochemical Conversion of AlkanesHans J. SchaferOrganisch-Chemisches Institut der Westfalischen Wilhelms-Universitat, Correns-Strasse 40, 4400 Munster,Germany
Chapter 18. Syntheses and Uses of Isotopically Labelled Alkanes and CycloalkanesMieczyslaw ZielinskiIsotope and Laboratory, Faculty of Chemistry, Jagiellonian University, Cracow, Poland
Marianna KanskaDepartment of Chemistry, The University of Warsaw, Warsaw, Poland
Derek V. BanthorpeDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, UK
Chapter 19. Natural Occurrence, Biochemistry and ToxicologyDerek V. BanthorpeDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, UK
Chapter 20. Inverted and Planar CarbonWilliam C. AgostaThe Rockefeller University, 1230 York Avenue, New York, NY 10021-6399, USA
Chapter 21. Radical Reactions of Alkanes and CycloalkanesGlen A. RussellDepartment of Chemistry, Iowa State University, Ames, Iowa 50011, USA
The Chemistry of Organophosphorus Compounds, Volume 2 (1992) (See Volume 1 in 1990,Volume 3 in 1993, Volume 4 in 1996)
Edited by Frank R. Hartley
Chapter 1. Structure and Bonding in Tertiary Phosphine ChalcogenidesD. G. GilheanyDepartment of Chemistry, St Patrick’s College, Maynooth, Co. Kildare, Ireland
Chapter 2. Structure and Stereochemistry of Secondary and Tertiary Phosphine ChalcogenidesM. J. GallagherSchool of Chemistry, University of New South Wales, PO Box 1, Kensington, New South Wales 2033,Australia
Chapter 3. Electrochemistry of Organophosphorus(V) CompoundsK. S. V. SanthanamChemical Physics Group, Tata Institute of Fundamental Research, Colaba, Bombay 400 005, India
Chapter 4. Photochemistry of Phosphine ChalcogenidesM. DankowskiDegussa AG, Inorganic Chemical Products Division, D-6000 Frankfurt, Germany
104
Chapter 5. Spectroscopy of Phosphine ChalcogenidesG. DavidsonDepartment of Chemistry, University of Nottingham, Nottingham NG7 2RD, UK
Chapter 6. Methods of Preparation of Phosphine ChalcogenidesA. K. BhattacharyaFACT Engineering and Design Organisation, New Delhi 110019, India
N. K. RoyIndian Agricultural Research Institute, New Delhi 110012, India
Chapter 7. Chemical Properties and Reactions of Phosphine ChalcogenidesR. S. EdmundsonRetired from Department of Chemistry, University of Bradford, Bradford, West Yorkshire BD7 1DP, UK
Chapter 8. Coordination Chemistry of Phosphine Chalcogenides and Their Analytical and CatalyticApplicationsT. S. LobanaDepartment of Chemistry, Guru Nanak Dev University, Amritsar 143 005, India
The Chemistry Hydroxyl, Ether and Peroxide Groups (1993)Edited by Saul Patai
Chapter 1. General and theoretical aspects of the −OH, −O− and −O−O− groups: Integration oftheory and experimentPeter PolitzerDepartment of Chemistry, University of New Orleans, New Orleans, Louisiana 70148, USA
Jane S. MurrayDepartment of Chemistry, University of New Orleans, New Orleans, Louisiana 70148, USA
Chapter 2. Structural chemistry of selected classes of alcohols, ethers and peroxidesIsrael GoldbergSchool of Chemistry, Sackler Faculty of Exact Sciences, Tel Aviv University, Ramat Aviv, 69978 Tel Aviv,Israel
Chapter 3. Chiroptical properties of alcohols, ethers and peroxidesA. GedankenDepartment of Chemistry, Bar-Ilan University, Ramat Gan 52100, Israel
Chapter 4. Thermochemistry of ethers, alcohols, arenols, enols and peroxidesSuzanne W. SlaydenDepartment of Chemistry, George Mason University, 4400 University Drive, Fairfax, VA 22030-4444, USA
Joel F. LiebmanDepartment of Chemistry and Biochemistry, University of Maryland, Baltimore County Campus, 5401Wilkens Ave., Baltimore, MD 21228-5398, USA
Chapter 5. Analytical methods for alcohols, phenols, ethers and peroxidesWalter T. Smith Jr.Department of Chemistry, University of Kentucky, Lexington, KY 40506-0055, USA
John M. PattersonDepartment of Chemistry, University of Kentucky, Lexington, KY 40506-0055, USA
105
Chapter 6. ESR and NMR spectroscopyJim IleyPhysical Organic Chemistry Research Group, The Open University, Milton Keynes, MK7 6AA, UK
Peter G. TaylorPhysical Organic Chemistry Research Group, The Open University, Milton Keynes, MK7 6AA, UK
Chapter 7. Photoelectron spectroscopy of alcohols, phenols, ethers and peroxidesM. Eckert-MaksicRudjer Boskovic Institute, Department of Organic Chemistry and Biochemistry, Zagreb, Republic ofCroatia
Chapter 8. Mass spectrometry of alcohols and ethersFrantisek TurecekDepartment of Chemistry, BG-10 University of Washington, Seattle, WA 98195, USA
Chapter 9. Electronic effects of ether and hydroxyl groupsJohn ShorterSchool of Chemistry, The University, Hull HU6 7RX, UK
Chapter 10. Syntheses and uses of isotopically labelled hydroxyl compounds and ethersMieczyslaw ZielinskiIsotope Laboratory, Faculty of Chemistry, Jagiellonian University, Cracow, Poland
Marianna KanskaDepartment of Chemistry, Warsaw University, Warsaw, Poland
Chapter 11. Epoxidation and hydroxylationYasuhiko SawakiDepartment of Applied Chemistry, Faculty of Engineering, Nagoya University, Chikusa-ku, Nagoya464-01, Japan
Chapter 12. Hydroxymethylation via radical intermediatesAkito IshidaThe Institute of Scientific and Industrial Research, Osaka University, Mihogaoka 8-1, Ibaraki 567, Japan
Setsuo TakamukuThe Institute of Scientific and Industrial Research, Osaka University, Mihogaoka 8-1, Ibaraki 567, Japan
Chapter 13. OzonolysisGury ZvilichovskyDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel
Bina ZvilichovskyMinistry of Commerce and Industry, Israel Fiber Institute, 5 Emek Refaim Street, Jerusalem 91080, Israel
Chapter 14. Rearrangements of alcohols, phenols, diols and peroxidesGy. SchneiderJozsef Attila University, Szeged, Hungary
Chapter 15. Rearrangements of open-chain and cyclic ethersM. BartoakDepartment of Organic Chemistry, Jozsef Attila University, Szeged, Hungary
106
Chapter 16. The electrochemistry of hydroxyl groups and ethersTatsuya ShonoDepartment of Synthetic Chemistry, Kyoto University, Kyoto 606-01, Japan
Chapter 17. Formations and reactions of peroxides in biological systemsEtsuo NikiResearch Center for Advanced Science and Technology, The University of Tokyo, 4-6-1 Komaba,Meguro-ku, Tokyo 153, Japan
Chapter 18. Diols and polyolsArpadMolnarDepartment of Organic Chemistry, Jozsef Attila University, Dom ter 8, H-6720 Szeged, Hungary
Chapter 19. Quinones: The present state of addition and substitution chemistryK. Thomas FinleyDepartment of Chemistry, State University College, Brockport, New York 14420, USA
The Chemistry of Organophosphorus Compounds, Volume 3 (1993) (See Volume 1 in 1990,Volume 2 in 1992, Volume 4 in 1996)
Edited by Frank R. Hartley
Chapter 1. Structure and Bonding in Phosphonium Ylides, Salts and PhosphoranesD. G. GilheanyDepartment of Chemistry, St Patrick’s College, Maynooth, Co. Kildare, Ireland
Chapter 2. Preparation, Properties and Reactions of Phosphonium SaltsH. J. CristauLaboratoire de Chimie Organique, URA 458, Ecole Nationale Superieure de Chimie, Universite deMontpellier, 8 rue de l’Ecole Normale, 34053 Montpellier Cedex 1, France
F. PlenatLaboratoire de Chimie Organique, URA 458, Ecole Nationale Superieure de Chimie, Universite deMontpellier, 8 rue de l’Ecole Normale, 34053 Montpellier Cedex 1, France
Chapter 3. Preparation, Properties and Reactions of PhosphoranesRamon BurgadaUniversite Pierre et Marie Curie, Laboratoire de Chimie des Organoelements, CNRS, 4 Place Jussieu,F-75252 Paris Cedex 05, France
Ralph SettonCNRS, Centre de Recherche sur la Matiere Divisee, 1B rue de la Ferollerie, F-45071 Orleans Cedex 2,France
Chapter 4. Structure, Bonding and Spectroscopic Properties of Phosphonium YlidesS. M. BachrachThe Michael Faraday Laboratories, Department of Chemistry, Northern Illinois University, DeKalb,Illinois 60115, USA
C. I. NitscheThe Michael Faraday Laboratories, Department of Chemistry, Northern Illinois University, DeKalb,Illinois 60115, USA
107
Chapter 5. Electrochemistry of Ylides, Phosphoranes and Phosphonium SaltsK. S. V. SanthanamChemical Physics Group, Tata Institute of Fundamental Research, Colaba, Bombay 400 005, India
Chapter 6. Photochemistry of Phosphonium Salts, Phosphoranes and YlidesM. DankowskiDegussa AG, ZN Wolfgang, AC-PT-PS, Postfach 13 45, 63403 Hanau, Germany
Chapter 7. Chemical Analysis of Organophosphorus CompoundsH. FeilchenfeldDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel
The Chemistry of Sulphur-Containing Functional Groups (1993)Edited by Saul Patai and Zvi Rappoport
Chapter 1. General and theoreticalTova HozDepartment of Chemistry, Bar-Ilan University, Ramat Gan 52900, Israel
Harold BaschDepartment of Chemistry, Bar-Ilan University, Ramat Gan 52900, Israel
Chapter 2. Structural chemistry of organosulfur compoundsBela RozsondaiStructural Chemistry Research Group of the Hungarian Academy of Sciences, Eotvos University, P.O.Box 117, H-1431 Budapest, Hungary
Chapter 3. The conformational analysis of sulphur-containing ringsF. G. RiddellDepartment of Chemistry, The University of St Andrews, St Andrews, KY169ST, Scotland, UK
Chapter 4. Thermochemistry of organosulphur compoundsJoel F. LiebmanDepartment of Chemistry and Biochemistry, University of Maryland, Baltimore County Campus, 5401Wilkens Ave., Baltimore, MD 21228-5398, USA
Kristine S. K. CrawfordDepartment of Chemistry and Biochemistry, University of Maryland, Baltimore County Campus, 5401Wilkens Ave., Baltimore, MD 21228-5398, USA
Suzanne W. SlaydenDepartment of Chemistry, George Mason University, 4400 University Drive, Fairfax, VA 22030-4444, USA
Chapter 5. NMR and ESR of organosulphur compoundsAlan R. BassindalePhysical Organic Research Group, Chemistry Department, The Open University, Milton Keynes, MK76AA, UK
James N. IleyPhysical Organic Research Group, Chemistry Department, The Open University, Milton Keynes, MK76AA, UK
108
Chapter 6. Mass spectra of organosulfur compoundsNico M. M. NibberingInstitute of Mass Spectrometry, University of Amsterdam, Nieuwe Achtergracht 129, 1018 WS Amsterdam,The Netherlands
Steen IngemannInstitute of Mass Spectrometry, University of Amsterdam, Nieuwe Achtergracht 129, 1018 WS Amsterdam,The Netherlands
Leo J. De KoningInstitute of Mass Spectrometry, University of Amsterdam, Nieuwe Achtergracht 129, 1018 WS Amsterdam,The Netherlands
Chapter 7. Carbon acidity resulting from sulfur substituentsGernot BocheFachbereich Chemie, Philipps-Universitat Marburg, Hans-Meerwein-Strasse, D-3550 Marburg, Germany
John C. W. LohrenzFachbereich Chemie, Philipps-Universitat Marburg, Hans-Meerwein-Strasse, D-3550 Marburg, Germany
Jerzy CioslowskiDepartment of Chemistry, The Florida State University, Tallahassee, Florida 32306-3006, USA
Wolfram KochInstitut fur Supercomputing und Angewandte Mathematik, Wissenschaftliches Zentrum, IBM DeutschlandGmbH, Tiergartenstr. 15, D-6900 Heidelberg, Germany
Chapter 8. Thiyl radicalsC. ChatgilialogluIstituto dei Composti del Carbonio Contenenti Eteroatomi e loro Applicazioni, CNR, 40064 Ozzano Emilia(Bologna), Italy
M. GuerraIstituto dei Composti del Carbonio Contenenti Eteroatomi e loro Applicazioni, CNR, 40064 Ozzano Emilia(Bologna), Italy
Chapter 9. Pyrolysis of organosulphur compoundsGonzalo MartinInstituto Venezolano de Investigaciones Cientificas (IVIC), Apartado 21827, Caracas 1020A, Venezuela
Chapter 10. Electrochemical behavior of organic molecules containing sulfurJacques SimonetLaboratoire d’Electrochimie Associe au CNRS, Universite de Rennes I, Campus de Beaulieu, 35042Rennes, France
Chapter 11. Syntheses and uses of isotopically labelled compounds with sulphur-containingfunctional groupsMieczyslaw ZielinskiIsotope Laboratory, Faculty of Chemistry, Jagiellonian University, Cracow, Poland
Marianna KanskaDepartment of Chemistry, University of Warsaw, Warsaw, Poland
Chapter 12. Soft metal ion-promoted reactions of organo-sulphur compoundsD. P. N. SatchellKing’s College London, Strand, London WC2R 2LS, UK
109
R. S. SatchellThe Hebrew University, Jerusalem
Chapter 13. Thiol—disulfide interchangeRajeeva SinghImmunoGen, Inc., 148 Sidney St., Cambridge, MA 02139
George M. WhitesidesDepartment of Chemistry, Harvard University, 12 Oxford St., Cambridge, MA 02138
Chapter 14. Vinyl sulfidesBoris A. TrofimovIrkutsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 664033Irkutsk, Russia
Bagrat A. ShainyanIrkutsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 664033Irkutsk, Russia
Chapter 15. High-coordinated sulfur compoundsJozef DrabowiczCentre of Molecular and Macromolecular Studies, Department of Organic Sulfur Compounds, PolishAcademy of Sciences, 90-363 Lodz, Sienkiewicza 112, Poland
Marian Mikołjczyk and Piotr ŁyzwaCentre of Molecular and Macromolecular Studies, Department of Organic Sulfur Compounds, PolishAcademy of Sciences, 90-363 Lodz, Sienkiewicza 112, Poland
Chapter 16. Biological activity of sulfoxides and sulfonesAsher KalirDepartment of Physiology and Pharmacology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv69978, Israel
Henry H. KalirDepartment of Neurobiology, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY10029, USA
Chapter 17. Organic sulfur in the geosphere: analysis, structures and chemical processesEitan B. KreinDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel
Synthesis of Lactones and Lactams (1993)Edited by Saul Patai and Zvi Rappoport
Chapter 1. The synthesis of lactones and lactams
Chapter 2. Appendix to ‘The synthesis of lactones and lactams’
110
The Chemistry of Enamines, Part 1 (1994)Edited by Zvi Rappoport
Chapter 1. Enamines: General and Theoretical AspectsGunter HafelingerInstitute of Organic Chemistry, University of Tubingen, Auf der Morgenstelle 18, D-72076 Tubingen,Germany
Hans-Georg MackInstitute of Physical and Theoretical Chemistry, University of Tubingen, Auf der Morgenstelle 8, D-72076Tubingen, Germany
Chapter 2. Structural Chemistry of Enamines: A Statistical ApproachBarbara J. OleksynFaculty of Chemistry, Jagiellonian University, ul. R. Ingardena 3, 30-060 Krakow, Poland
Katarzyna StadnickaFaculty of Chemistry, Jagiellonian University, ul. R. Ingardena 3, 30-060 Krakow, Poland
Jan SliwinskiFaculty of Chemistry, Jagiellonian University, ul. R. Ingardena 3, 30-060 Krakow, Poland
Chapter 3. Configuration, Conformation and Chiroptical Properties of EnaminesOtakar CervinkaDepartment of Organic Chemistry, Institute of Chemical Technology, 166 28 Prague 6, Czech Republic
Chapter 4. Thermochemistry of EnaminesJoel F. LiebmanDepartment of Chemistry and Biochemistry, University of Maryland, Baltimore County Campus, 5401Wilkens Avenue, Baltimore, Maryland 21228-5398, USA
H. Mark PerksDepartment of Chemistry, The Johns Hopkins University, Charles and 34th Streets, Baltimore, Maryland21218, USA
Chapter 5. NMR SpectraJose Luis ChiaraInstituto de Quımica Organica, C.S.I.C., Juan de la Cierva, 3, 28006 Madrid, Spain
Antonio Gomez-SanchezDepartamento de Quımica Organica, Facultad de Quımica, Universidad de Sevilla, Apartado de Correos553, 41071 Sevilla, Spain
Chapter 6. Static and Dynamic Stereochemistry of Acceptor-Substituted EnaminesJan SandstromDivision of Organic Chemistry 3, Chemical Center, University of Lund, P.O. Box 124, S-22100 Lund,Sweden
Chapter 7. The Reactivity of Ionized Enamines in the Gas PhasePierre LongevialleInstitut de Chimie des Substances Naturelles du Centre National de la Recherche Scientifique, 91190 Gifsur Yvette, France
Chapter 8. The Electrochemistry of EnaminesTatsuya ShonoDepartment of Synthetic Chemistry, Kyoto University, Kyoto 606-01 Japan
111
Chapter 9. Preparation of EnaminesOtakar CervinkaDepartment of Organic Chemistry, Institute of Chemical-Technology, 166 28 Prague 6, Czech Republic
Chapter 10. Enaminones as SynthonesUwe KucklanderInstitut fur Pharmazeutische Chemie der Heinrich-Heine-Universitat Dusseldorf, Universitatsstr. 1, 40225Dusseldorf 1, Germany
Chapter 11. Photochemistry of Enamines and EnaminonesMiles G. SiegelDepartment of Chemistry, The University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA
Jeffrey D. WinklerDepartment of Chemistry, The University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA
Chapter 12. Radiation Chemistry of EnaminesZeev B. AlfassiDepartment of Nuclear Engineering, Ben Gurion University of the Negev, Beersheva 84105, Israel
Chapter 13. Acidity and Basicity of EnaminesJavier CatalanDepartamento de Quimica Fisica Aplicada, Universidad Autonoma de Madrid, Cantoblanco, Madrid28049, Spain
Francisco Garcia BlancoDepartamento de Quimica Fisica, Facultad de Farmacia, Ins. Pluridisciplinar Universidad Complutensede Madrid, Madrid 28040, Spain
Chapter 14. Electrophilic and Nucleophilic Substitution and Addition Reactions of EnaminesP. W. HickmottUniversity of Natal, Durban, Natal, South Africa
Chapter 15. Radical Reactions of EnaminesShekhar V. KulkarniDepartment of Chemistry, Purdue University, West Lafayette, Indiana 47907, USA
Chapter 16. Rearrangements and Tautomerizations of EnaminesZhi-Tang HuangInstitute of Chemistry, Academia Sinica, Beijing 100080, People’s Republic of China
Mei-Xiang WangInstitute of Chemistry, Academia Sinica, Beijing 100080, People’s Republic of China
Chapter 17. Oxidation and Reduction of EnaminesGiuliana PitaccoDipartimento di Scienze Chimiche, Universita degli Studi di Trieste, Via Licio Giorgieri 1, 34135 Trieste,Italy
Ennio ValentinDipartimento di Scienze Chimiche, Universita degli Studi di Trieste, Via Licio Giorgieri 1, 34135 Trieste,Italy
Chapter 18. Cycloadditions to EnaminesRafael ChinchillaDepartment of Organic Chemistry, University of Uppsala, Box 531, S-751 21 Uppsala, Sweden
112
Jan-E. BackvallDepartment of Organic Chemistry, University of Uppsala, Box 531, S-751 21 Uppsala, Sweden
Chapter 19. Mechanisms of Enamine HydrolysisJames R. KeeffeDepartment of Chemistry and Biochemistry, San Francisco State University, San Francisco, California94132, USA
A. Jerry KresgeDepartment of Chemistry, University of Toronto, Toronto, Ontario M5S 1A1, Canada
Chapter 20. Syntheses and Uses of Isotopically Labelled EnaminesZielinski MieczyslawIsotope Laboratory, Faculty of Chemistry, Jagiellonian University, ul. Ingardena 3, 30-060 Krakow,Poland
Marianna KanskaDepartment of Chemistry, Warsaw University, Pasteura str. 1, 02-083 Warsaw, Poland
Chapter 21. Biochemistry of EnaminesFrank JordanDepartment of Chemistry, Rutgers, the State University of New Jersey, Newark, New Jersey, USA
Chapter 22. 1, 1-EnediaminesZhi-Tang HuangInstitute of Chemistry, Academia Sinica, Beijing 100080, People’s Republic of China
Wang Mei-XiangInstitute of Chemistry, Academia Sinica, Beijing 100080, People’s Republic of China
Chapter 23. Heterocyclic Synthesis from EnaminesGerhard V. BoydDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem, Israel
Chapter 24. Synthesis of N-Acylenamines from Carbonyl Compounds and NitrilesSerge M. LukyanovInstitute of Physical and Organic Chemistry, Rostov University, 344711 Rostov on Don, Russia
Chapter 25. Lithium Enamides—Lithium Salts of Azomethine DerivativesShimon ShatzmillerThe Beverly and Raymond Sackler Faculty of Exact Sciences, School of Chemistry, Tel-Aviv University,Ramat-Aviv, Tel-Aviv 69978, Israel
Rami LidorThe Beverly and Raymond Sackler Faculty of Exact Sciences, School of Chemistry, Tel-Aviv University,Ramat-Aviv, Tel-Aviv 69978, Israel
Chapter 26. Reactions of DienaminesP. W. HickmottUniversity of Natal, Durban, South AfricaEdited by Saul Patai
Chapter 1. General and Theoretical AspectsShigeru NagaseDepartment of Chemistry, Faculty of Education, Yokohama National University, Yokohama 240, Japan
113
Chapter 2. Structural Chemistry of Organic Compounds Containing Arsenic, Antimony andBismuthD. B. SowerbyDepartment of Chemistry, University of Nottingham, Nottingham NG7 2RD, UK
Chapter 3. Optically Active Arsines: Preparation, Uses and Chiroptical PropertiesS. B. WildResearch School of Chemistry, Institute of Advanced Studies, Australian National University, Canberra,A.C.T. 0200, Australia
Chapter 4. Thermochemistry of Organoarsenic, Antimony and Bismuth CompoundsJoel F. LiebmanDepartment of Chemistry and Biochemistry, University of Maryland, Baltimore County Campus, 5401Wilkens Avenue, Baltimore, Maryland 21228-5398, USA
Jose Artur Martinho SimoesDepartmento de Engenharia Quimica, Instituto Superior Tecnico, 1096 Lisboa Codex, Portugal
Suzanne W. SlaydenDepartment of Chemistry, George Mason University, 4400 University Drive, Fairfax, Virginia 22030-4444,USA
Chapter 5. Detection, Identification and DeterminationT. R. CromptonHill Cottage, Pen Marian, Nr Llangoed, Beaumaris, Anglesey, Gwynedd, Wales LL588SU, UK
Chapter 6. Mass Spectra of the Organometallic Compounds of As, Sb, and BiYurii S. NekrasovInstitute of Organo-Element Compounds, Russian Academy of Sciences, Moscow, Russia, CIS, 117334
Dmitri V. ZagorevskiiInstitute of Organo-Element Compounds, Russian Academy of Sciences, Moscow, Russia, CIS, 117334
Chapter 7. PES of Organic Derivatives of As, Sb and BiL. SzepesGeneral and Inorganic Chemistry Department, Eotvos Lorand University, H-1518 Budapest, P.O. Box 32,Hungary
A. NagyGeneral and Inorganic Chemistry Department, Eotvos Lorand University, H-1518 Budapest, P.O. Box 32,Hungary
L. ZanathyGeneral and Inorganic Chemistry Department, Eotvos Lorand University, H-1518 Budapest, P.O. Box 32,Hungary
Chapter 8. Lewis Acidity, Basicity, H-bonding and Complexing of Organic Arsenic, Antimony andBismuth CompoundsKatharina C. H. LangeInstitut fur Anorganische und Analytische Chemie, Technische Universitat Berlin, Strasse des 17. Juni 135,D-10623 Berlin, Germany
Thomas M. KlapotkeInstitut fur Anorganische und Analytische Chemie, Technische Universitat Berlin, Strasse des 17. Juni 135,D-10623 Berlin, Germany
114
Chapter 9. Substituent Effects of Arsenic, Antimony and Bismuth GroupsMarvin ChartonChemistry Department, School of Liberal Arts and Sciences, Pratt Institute, Brooklyn, New York 11205,USA
Chapter 10. Thermochromism of Organometallic Derivatives Containing As, Sb or BiH. J. BreunigUniversitat Bremen, Fachbereich 2 (Chemie), Postfach 330440, D-28334 Bremen Germany
Chapter 11. ElectrochemistryMerete Folmer NielsenDepartment of Chemistry, University of Copenhagen, Denmark
Chapter 12. Radical Intermediates in Radiation Chemistry of As, Sb and Bi CompoundsM. GeoffroyDepartment of Physical Chemistry, University of Geneva, 30 Quai Ernest Ansermet, 1211 Geneva,Switzerland
T. BerclazDepartment of Physical Chemistry, University of Geneva, 30 Quai Ernest Ansermet, 1211 Geneva,Switzerland
Chapter 13. ThermolysisC. A. McAuliffeDepartment of Chemistry, University of Manchester Institute of Science and Technology, Manchester M60IQD, UK
A. G. MackieDepartment of Chemistry, University of Manchester Institute of Science and Technology, Manchester M60IQD, UK
Chapter 14. Organoarsenic and Organoantimony HomocyclesHans Joachim BreunigUniversitat Bremen, Fachbereich 2 (Chemie), Postfach 330440, D-28334 Bremen, Germany
Chapter 15. Syntheses and Uses of Isotopically Labelled Compounds of Bismuth, Antimony andArsenicMieczyslaw ZielinskiIsotope Laboratory, Faculty of Chemistry, Jagiellonian University, Cracow, Poland
Marianna KanskaDepartment of Chemistry, The University of Warsaw, Warsaw, Poland
Chapter 16. Arsonium, Stibonium and Bismuthonium Ylides and IminesDouglas LloydDepartment of Chemistry, Purdie Building, University of St. Andrews, St. Andrews, Fife, KY16 9ST,Scotland, UK
Ian GosneyDepartment of Chemistry, The University of Edinburgh, Edinburgh, EH9 3JJ, Scotland, UK
Chapter 17. The Biochemistry of Arsenic, Bismuth and AntimonyKilian DillThe Department of Chemistry, Clemson University, Clemson, South Carolina 29634-1905, USA
115
Evelyn L. McGownThe Chemistry Branch, Blood Research Division, Letterman Army Institute of Research, Presidio of SanFrancisco, California 94129-6800, USA
Chapter 18. Pharmacology and Toxicology of Organic Bismuth, Arsenic and Antimony CompoundsUri WormserDepartment of Pharmacology, School of Pharmacy, Faculty of Medicine, The Hebrew University ofJerusalem, Jerusalem, Israel
Isaac NirDepartment of Pharmacology, School of Pharmacy, Faculty of Medicine, The Hebrew University ofJerusalem, Jerusalem, Israel
Chapter 19. Safety and Environmental EffectsShigeru MaedaDepartment of Applied Chemistry and Chemical Engineering, Faculty of Engineering, KagoshimaUniversity, 1-21-40 Korimoto, Kagoshima 890, Japan
Chapter 20. Syntheses of Organoantimony and Organobismuth CompoundsKin-Ya AkibaDepartment of Chemistry, University of Hiroshima, 1-3-1 Kagamiyama, Higashi-Hiroshima, 724, Japan
Yohsuke YamamotoDepartment of Chemistry, University of Hiroshima, 1-3-1 Kagamiyama, Higashi-Hiroshima, 724, Japan
Chapter 21. Syntheses of Organoarsenic CompoundsYohsuke YamamotoDepartment of Chemistry, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima 724, Japan
Kin-Ya AkibaDepartment of Chemistry, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima 724, Japan
The Chemistry of Triple Bonded Functional Groups (1994)Edited by Saul Patai
Chapter 1. The Nature of the Triple BondHarold BaschDepartment of Chemistry, Bar Ilan University, Ramat Gan 52900, Israel
Tova HozDepartment of Chemistry, Bar Ilan University, Ramat Gan 52900, Israel
Chapter 2. Structural Chemistry of Triple-bonded GroupsFrank H. AllenCambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, England
Stephanie E. GarnerCambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, England
Chapter 3. Photoelectron Spectra of Systems with Triple Bonds between Main GroupAtoms—Recent StudiesRolf GleiterOrganisch-Chemisches Institut der Universitat Heidelberg, Im Neuenheimer Feld 270, D-69120Heidelberg, Germany
116
Wolfgang SchaferBoehringer Mannheim GmbH, Sandhofer Str. 116, D-68305 Mannheim, Germany
Chapter 4. Analytical Aspects of Alkynes, Nitriles, Cyanates, Thiocyanates, Diazonium Compoundsand Their Isomeric Functional GroupsJacob ZabickyThe Institutes for Applied Research, Ben-Gurion University of the Negev, Beer-Sheva 84110, Israel
Chapter 5. Electronic Effects of Cyano, Isocyano, Acetylenic and Diazonio GroupsJohn ShorterSchool of Chemistry, University of Hull, Hull HU6 7RX, UK
Chapter 6. Advances in Acetylene ChemistryG. V. BoydDepartment of Organic Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel
Chapter 7. Photochemistry and Radiation ChemistryWilliam M. HorspoolDepartment of Chemistry, The University of Dundee, Dundee, DD1 4HN, Scotland, UK
Chapter 8. The Thermochemistry of the C≡C BondT. Kasprzycka-GuttmanDepartment of Chemistry, University of Warsaw, 02-093 Warsaw, Pasteura 1, Poland
Chapter 9. Rearrangements Involving Triple Bonded GroupsD. WhittakerDepartment of Chemistry, University of Liverpool, L69 3BX, UK
Chapter 10. The Electrochemistry of the Triple BondHans ViertlerInstituto de Quımica, Universidade de Sao Paulo, 01498 Sao Paulo, Brazil
Vera L. PardiniInstituto de Quımica, Universidade de Sao Paulo, 01498 Sao Paulo, Brazil
Reinaldo R. VargasInstituto de Quımica, Universidade de Sao Paulo, 01498 Sao Paulo, Brazil
Chapter 11. Syntheses and Uses of Isotopically Labelled X≡Y GroupsKenneth C. WestawayDepartment of Chemistry, Laurentian University, Ramsey Lake Road, Sudbury Ontario P3E 2C6, Canada
Peter J. SmithDepartment of Chemistry and Chemical Engineering, University of Saskatchewan, Saskatoon,Saskatchewan, Canada
Chapter 12. Biochemistry of Triple-Bonded Functional GroupsDerek V. BanthorpeDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H OAH, UK
Chapter 13. Pharmacology of Acetylenic DerivativesZvi Ben-ZviDepartment of Clinical Pharmacology, Ben-Gurion University of the Negev and Soroka Medical Center,Beer Sheva, Israel
117
Abraham DanonDepartment of Clinical Pharmacology, Ben-Gurion University of the Negev and Soroka Medical Center,Beer Sheva, Israel
Chapter 14. Polycyano Compounds
Renate DworczakKarl-Franzens University of Graz, Graz, Austria
Hans JunekKarl-Franzens University of Graz, Graz, Austria
Chapter 15. Electrophilic Additions to Functional Groups Containing a Triple BondWiendelt DrenthDepartment of Organic Chemistry, Utrecht University, Utrecht, The Netherlands Ovidiuslaan 4, 3584 AWUtrecht, The Netherlands
Chapter 16. Free-Radical Addition Involving C≡C Triple BondsC. ChatgilialogluI.Co.C.E.A., Consiglio Nazionale delle Ricerche, Via Gobetti 101, 40129 Bologna, Italy
C. FerreriDipartimento di Chimica Organica e Biologica, Universita di Napoli, Via Mezzocannone 16, 80134Napoli, Italy
Chapter 17. Synthesis and Properties of Acetylenic PolymersHideki ShirakawaInstitute of Materials Science, University of Tsukuba, Tsukuba, Ibaraki 305, Japan
Toshio MasudaDepartment of Polymer Chemistry, Kyoto University, Kyoto 606-01, Japan
Kenji TakedaResearch Center, Japan Synthetic Rubber Co., Ltd, 25, Miyukigaoka, Tsukuba, Ibaraki 305, Japan
Chapter 18. Arynes and HeteroarynesHarold HartDepartment of Chemistry, Michigan State University, 320 Chemistry Building, East Lansing, Michigan48824-1322, USA
Chapter 19. Ynol Ethers and EstersPeter J. StangDepartment of Chemistry, The University of Utah, Salt Lake City, Utah 84112, USA
Viktor V. ZhdankinDepartment of Chemistry, University of Minnesota-Duluth, Minnesota 55812, USA
Chapter 20. Alkynyl(Phenyl)Iodonium and Related SpeciesPeter J. StangDepartment of Chemistry, The University of Utah, Salt Lake City, Utah 84112, USA
Chapter 21. Mass Spectrometry Studies on Molecules and Ions with C−C BondsChrys WesdemiotisDepartment of Chemistry, The University of Akron, Akron, Ohio 44325-3601, USA
Michael J. PolceDepartment of Chemistry, The University of Akron, Akron, Ohio 44325-3601, USA
118
Sarka BeranovaDepartment of Chemistry, The University of Akron, Akron, Ohio 44325-3601, USA
The Syntheses of Sulphones, Sulphoxides and Cyclic Sulphides (1995)Edited by Saul Patai and Zvi Rappoport
Chapter 1. Synthesis of Open-Chain SulfonesKurt SchankFachrichtung 13.2 Organische Chemie, Universitat des Saarlandes, D-6600 Saarbrucken, FRG
Chapter 2. Appendix to ‘Synthesis of Open-Chain Sulfones’Kurt SchankFachrichtung 11.2 Organische Chemie, Universitat des Saariandes, D-66041 Saarbrucken, Germany
Norbert SchottFachrichtung 11.2 Organische Chemie, Universitat des Saariandes, D-66041 Saarbrucken, Germany
Chapter 3. Synthesis of SulphoxidesJozef DrabowiczPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, 90-362 Lodz, Boczna 5, Poland
Piotr KielbasinskiPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, 90-362 Lodz, Boczna 5, Poland
Marian MikolajczykPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, 90-362 Lodz, Boczna 5, Poland
Chapter 4. Appendix to ‘Synthesis of Sulphoxides’Jozef DrabowiczPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363 Lodz, Poland
Piotr KielbasinskiPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363 Lodz, Poland
Marian MikolajczykPolish Academy of Sciences, Centre of Molecular and Macromolecular Studies, Department of OrganicSulphur Compounds, Sienkiewicza 112, 90-363 Lodz, Poland
Chapter 5. Cyclic Sulfones and SulfoxidesUri ZollerHaifa University, Oranim, Israel
Chapter 6. Appendix to ‘Cyclic Sulfones and Sulfoxides’
Uri ZollerHaifa University, Oranim, Israel
Chapter 7. Cyclic SulfidesGiuseppe CapozziCentro C. N. R. ‘Chimica e Struttura dei Composti Eterociclici’, c/o Dipartimento di Chimica Organica,Universita’ di Firenze, via G. Capponi 9, 50121 Firenze, Italy
119
Stefano MenichettiCentro C. N. R. ‘Chimica e Struttura dei Composti Eterociclici’, c/o Dipartimento di Chimica Organica,Universita’ di Firenze, via G. Capponi 9, 50121 Firenze, Italy
Cristina NativiCentro C. N. R. ‘Chimica e Struttura dei Composti Eterociclici’, c/o Dipartimento di Chimica Organica,Universita’ di Firenze, via G. Capponi 9, 50121 Firenze, Italy
The Chemistry of the Cyclopropyl Group (1995) (See volume 1 in 1987)
Edited by Zvi Rappoport
Thermal Stereomutations of Cyclopropanes and VinylcyclopropanesJohn E. BaldwinSyracuse University, Department of Chemistry, Syracuse, NY 13244, USA
Cyclopropyl Homoconjugation—Experimental Facts and Interpretations
Cyclopropyl Homoconjugation, Homoaromaticity and Homoantiaromaticity—Theoretical Aspectsand AnalysisRonald F. ChildsMcMaster University, Department of Chemistry, Hamilton, Ontario, Canada L8S 4M1
Prologue: History of Cyclopropane Derivatives Before 1916James Bryant ConantHarvard University, Department of Chemistry, Cambridge, MA, USA
Cyclopropyl Homoconjugation—Experimental Facts and Interpretations
Cyclopropyl Homoconjugation, Homoaromaticity and Homoantiaromaticity—Theoretical Aspectsand Analysis
General and Theoretical Aspects of the Cyclopropyl GroupDieter CremerUniversity of Goteborg, Department of Theoretical Chemistry, Kemigarden 3, Goteborg, Sweden S-41296
Cyclopropyl Homoconjugation—Experimental Facts and InterpretationsGeorge EliaMcMaster University, Department of Chemistry, Hamilton, Ontario, CanadaL8S 4M1
Organometallic DerivativesZeev GoldschmidtBar-Ilan University, Department of Chemistry, Ramat-Gan52900, Israel
CycloproparenesBrian HaltonVictoria University of Wellington, Department of Chemistry, PO Box 600, Wellington, New Zealand
[1.1.1]PropellanesPiotr KaszynskiVanderbilt University, Department of Chemistry, Nashville, TN 37235, USA
120
Cyclopropyl Homoconjugation, Homoaromaticity and Homoantiaromaticity—Theoretical Aspectsand Analysis
General and Theoretical Aspects of the Cyclopropyl GroupElfi KrakaUniversity of Goteborg, Department of Theoretical Chemistry, Kemigarden 3, Goteborg, Sweden S-41296
ThermochemistryJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 5401 WilkensAvenue, Baltimore, MA 21228-5398, USA
Spiroannulated CyclopropanesKirill A LukinThe University of Chicago, Department of Chemistry, 5735 South Ellis Avenue, Chicago, IL 60637, USA
Metal Catalysed CyclopropanationM. Anthony McKerveyThe Queen’s University, School of Chemistry, Belfast, Northern Ireland, UK BT9 5AG
[1.1.1]PropellanesJosef MichlUniversity of Colorado, Department of Chemistry and Biochemistry, Boulder, CO 80309-0215, USA
Recent Advances in Synthesis of CyclopropanesShinya NishidaHokkaido University, Department of Chemistry, Faculty of Science, Sapporo 060, Japan
Recent Advances in Synthesis of CyclopropanesMasakazu OhkitaHokkaido University, Department of Chemistry, Faculty of Science, Sapporo 060, Japan
Long-Lived Cyclopropylcarbinyl CationsGeorge A. OlahUniversity of Southern California, Loker Hydrocarbon Research Institute and Department of Chemistry,Los Angeles, CA 90089-1661, USA
Long-Lived Cyclopropylcarbinyl CationsPrakash V. ReddyUniversity of Southern California, Loker Hydrocarbon Research Institute and Department of Chemistry,Los Angeles, CA 90089-1661, USA
Structural ChemistryBela RozsondaiResearch Group of the Hungarian Academy of Sciences, Eotvos University, P.O. Box 117, Budapest,Hungary H-1431
Long-Lived Cyclopropylcarbinyl CationsG. K. Surya PrakashUniversity of Southern California, Loker Hydrocarbon Research Institute and Department of Chemistry,Los Angeles, CA 90089-1661, USA
121
General and Theoretical Aspects of the Cyclopropyl GroupKalman Josef SzaboUniversity of Goteborg, Department of Theoretical Chemistry, Kemigarden 3, Goteborg, Sweden S-41296
Recent Advances in Synthesis of CyclopropanesTakashi TsujiHokkaido University, Department of Chemistry, Faculty of Science, Sapporo 060, Japan
Metal Catalysed CyclopropanationTao YeThe Queen’s University, School of Chemistry, Belfast, Northern Ireland, UK BT9 5AG
Spiroannulated CyclopropanesNikolai S ZefirovMoscow State University, Department of Chemistry, Moscow, Russia
Cyclopropane PhotochemistryHoward E. ZimmermanUniversity of Wisconsin, Chemistry Department, Madison, WI 53706, USA
The Chemistry of Halides, Pseudo-Halides and Azides (1995)Edited by Saul Patai and Zvi Rappoport
Radiation ChemistryZeev B. AlfassiBenGurion University of the Negev, Department of Nuclear Engineering, Beer Sheva, Israel
Eliminations Involving Carbon–Halogen Bonds and Leading to Highly Strained RingsMark S. BairdUniversity of Wales, Department of Chemistry, Gwynedd, Bangor, Wales, UK LL57 2UW
Recent Advances in the Organic Chemistry of AstatineKlara BereiKFKI Atomic Energy Research Institute, Budapest, Hungary
Eliminations Involving Carbon–Halogen Bonds and Leading to Highly Strained RingsIvan G. BolesovMoscow State University, Department of Chemistry, Moscow, Russia
Conformational and Chiroptical Properties of Alkyl HalidesJames H. BrewsterPurdue University, Department of Chemistry, West Lafayette, IN 47907-3699, USA
Electrochemistry of the Carbon–Halogen BondJoseph CasanovaCalifornia State University, Department of Chemistry, Los Angeles, CA 90032, USA
Pyrolysis of Organic HalidesGabriel ChuchaniInstituto Venezolano de Investigaciones Cientıficas (IVIC), Department of Chemistry, Apartado 21827,Caracas, Venezuela 1020-A
122
Recent Advances in the Photochemistry of the Carbon–Halogen BondJan CornelisseLeiden Institute of Chemistry, Leiden University, Gorlaeus Laboratories, 2300 RA Leiden, The Netherlands9502
NMR SpectroscopyBrian EverattCiba Geigy PLC, Hulley Road, Macclesfield, Cheshire, UKSK10 2NX
Atmospheric Chemistry of Organic HalidesJoseph S. FranciscoPurdue University, Department of Chemistry and Department of Earth and Atmospheric Sciences, WestLafayette, IN, USA
Electron Spin Resonance and Nuclear Quadrupole ResonanceMichel GeoffroyUniversite de Geneve, Sciences II, Department de Chimie Physique, 30 Quai Ernest-Ansermet, Geneve 4,Switzerland 1211
Reactions of Organic Halides Mediated by Transition Metal CompoundsJames R. GreenDepartment of Chemistry and Biochemistry, University of Windsor, Windsor, Ontario, Canada N9B 3P4
Some Synthetic Uses of HalidesJeff HoyleNova ScotiaAgricultural College, Chemistry and Soil Science Department, Truro, Nova Scotia, Canada B2N 5E3
Syntheses and Uses of Isotopically Labelled Organic HalidesMarianna KanskaWarsaw University, Department of Chemistry, Warsaw, Poland
Biochemistry of halogenated organic compoundsKenneth L. KirkNational Institutes of Health, Department of Health & Human Services, Bethesda, MA 20892, USA
Photoelectron Spectra of Compounds with Carbon–Halogen BondsL. KlasincInstitute Rugjer Boskovic, Zagreb, Croatia
Halonium IonsGerald F. KoserThe University of Akron, Department of Chemistry, Akron, OH 44325-3601, USA
ThermochemistryJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 5401 Wilkens Ave.,Baltimore, MA 21228-5398, USA
Recent Advances in the Photochemistry of the Carbon–Halogen BondGerrit LodderLeiden Institute of Chemistry, Leiden University, Gorlaeus Laboratories, 2300 RA Leiden, The Netherlands9502
123
Electron Spin Resonance and Nuclear Quadrupole ResonanceEdwin A. C. LuckenUniversite de Geneve, Sciences II, Department de Chimie Physique, 30 Quai Ernest-Ansermet, Geneve 4,Switzerland 1211
Positive Halogen CompoundsHisham G. Lutfisouthern Illinois University, Department of Chemistry and Biochemistry, Carbondale, IL 62901-4409, USA
ThermochemistryW. Gary MallardNational Institute of Standards and Technology, Chemical Kinetics and Thermodynamics Division,Gaithersburg, MA 20899-0001, USA
Photoelectron Spectra of Compounds with Carbon–Halogen BondsS. P. McGlynnLouisiana State University, Department of Chemistry, Baton Rouge, LA 70803, USA
Positive Halogen CompoundsCAL Y. Meyerssouthern Illinois University, Department of Chemistry and Biochemistry, Carbondale, IL 62901-4409, USA
General and Theoretical Aspects of the C−X bonds (X=F, Cl, Br, I): Integration of Theory andExperimentJane S. MurrayUniversity of New Orleans, Department of Chemistry, New Orleans, LA 70148, USA
Photoelectron Spectra of Compounds with Carbon–Halogen BondsI. NovakNational University of Singapore, Department of Chemistry, Singapore
Structural ChemistryHeinz OberhammerUniversitat Tubingen, Institut fur Physikalische und Theoretische Chemie, Tubingen, Germany 76072
Mass spectra and gas-phase ion chemistry of halogen-containing compoundsCristina ParadisiCentro Studio Meccanismi Reazioni Organiche del CNR, Dipartimento di Chimica Organicadell’Universita, Via Marzolo 1, Padova, Italy 35131
Mossbauer SpectroscopyR. V. ParishUMIST, Department of Chemistry, PO Box 88, Manchester, UKM60 1QD
Recent Advances in the SRN1 Reaction of Organic HalidesAlicia B. PenenoryFacultad de Ciencias Quımicas, Departmento de Quımica Organica, Universidad Nacional de Cordoba,INFIQC, Suc. 16, CC 61, Cordoba, Argentina 5016
Recent Advances in the SRN1 Reaction of Organic HalidesAdriana B. PieriniFacultad de Ciencias Quımicas, Departmento de Quımica Organica, Universidad Nacional de Cordoba,INFIQC, Suc. 16, CC 61, Cordoba, Argentina 5016
124
General and Theoretical Aspects of the C−X bonds (X=F, Cl, Br, I): Integration of Theory andExperimentPeter PolitzerUniversity of New Orleans, Department of Chemistry, New Orleans, LA 70148, USA
Electrochemistry of the Carbon–Halogen BondV. Prakash ReddyUniversity of Miami, Department of Chemistry, Coral Gables, FL 33124, USA
Recent Advances in the SRN1 Reaction of Organic HalidesRoberto A. RossiFacultad de Ciencias Quımicas, Departmento de Quımica Organica, Universidad Nacional de Cordoba,INFIQC, Suc. 16, CC 61, Cordoba, Argentina 5016
The Formation of the C−F Bond: The Last Twelve YearsShlomo RozenTelAviv University, School of Chemistry, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv,Israel 69978
Formation of Carbon–Halogen Bonds (Cl, Br, I)Yoel SassonThe Hebrew University of Jerusalem, Casali Institute of Applied Chemistry, Jerusalem, Israel 91904
ThermochemistrySuzanne W. SlaydenGeorgeMason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA
NMR SpectroscopyPeter TaylorThe Open University, Chemistry Department, Milton Keynes, Bucks, UK MK7 6AA
Recent Advances in the Organic Chemistry of AstatineLaszlo VasarosKFKI Atomic Energy Research Institute, Budapest, Hungary
Mass spectra and gas-phase ion chemistry of halogen-containing compoundsUmberto VettoriCentro Studio Stabilita e Reattivita dei Composti di Coordinazione del CNR, Via Marzolo 1, Padova, Italy35131
Atmospheric Chemistry of Organic HalidesIan H. WilliamsUniversity of Bath, School of Chemistry, Bath, UKBA2 7AY
Syntheses and Uses of Isotopically Labelled Organic HalidesMieczysłlaw ZielinskiJagiellonian University, Isotope Laboratory, Faculty of Chemistry, Cracow, Poland
Functionalization of Organic Molecules by Xenon FluoridesMarko ZupanUniversity of Ljubljana, Laboratory for Organic and Bioorganic Chemistry, Department of Chemistry and‘J. Stefan’ Institute, Ljubljana, Slovenia
125
The Chemistry of Organic Germanium, Tin and Lead Compounds, Volume 1 (1995)(See Volume 2 in 2003)
Edited by Saul Patai
The Nature of the C−M Bond (M=Ge, Sn, Pb)Harold BaschBar-Ilan University, Department of Chemistry, Ramat-Gan52900, Israel
Photoelectron Spectroscopy (PES) of Organometallic Compounds with C−M (M=Ge, Sn, Pb) BondsCarla CaulettiUniversita di Roma ‘La Sapienza’, Dipartimento di Chimica, Piazzale Aldo Moro, 5, Rome, Italy 00185
Substituent Effects of Germanium, Tin and Lead GroupsMarvin ChartonSchool of Liberal Arts and Sciences, Pratt Institute, Chemistry Department, Brooklyn, NY 11205, USA
The Environmental Methylation of Germanium, Tin and LeadP. J. CraigDe Montfort University, Department of Chemistry, The Gateway, Leicester, UK LE1 9BH
Synthesis of M(IV) Organometallic Compounds, where M=Ge, Sn, PbMarcel GielenFree University of Brussels, Pleinlaan 2, Brussels, Belgium B-1050
The Photochemistry of Organometallic Compounds of Germanium and LeadCharles M. GordonDublinCity University, School of Chemical Sciences, Dublin 9, Ireland
Analytical Aspects of Organogermanium Compounds
Analytical Aspects of Organolead Compounds
Analytical Aspects of Organotin CompoundsSarina GrinbergInstitutes for Applied Research, Ben-Gurion University of the Negev, Beer-Sheva, Israel 84110
The Nature of the C−M Bond (M=Ge, Sn, Pb)Tova HozBar-Ilan University, Department of Chemistry, Ramat-Gan52900, Israel
Toxicity of Organogermanium CompoundsL. M. IgnatovichLatvian Institute of Organic Synthesis, Riga, LatviaLV 1006
ESR of Organogermanium, Organotin and Organolead RadicalsJim IleyThe Open University, Physical Organic Chemistry Research Group, Chemistry Department, MiltonKeynes, UK MK7 6AA
Stereochemistry and Conformation of Organogermanium, Organotin and Organolead CompoundsJill A. JablonowskiUniversity of South Carolina, Department of Chemistry and Biochemistry, Columbia, SC 29208, USA
126
Syntheses and Uses of Isotopically Labelled Organic Derivatives of Ge, Sn and PbHelen JolyLaurentian University, Department of Chemistry, Sudbury, Ontario, Canada P3E 2C6
Acidity, Complexing, Basicity and H-Bonding of Organic Germanium, Tin and Lead Compounds:Experimental and Computational ResultsThomas M. KlapotkeTechnische Universitat Berlin, Institut fur Anorganische und Analytische Chemie, Strasse des 17. Juni 135,Berlin, Germany D-10623
ThermochemistryJoel F. LiebmanDepartment of Chemistry and Biochemistry, University of Maryland Baltimore County, 5401 WilkensAvenue, Baltimore, MD 21228-5398, USA
The Photochemistry of Organometallic Compounds of Germanium and LeadConor LongDublin City University, School of Chemical Sciences, Dublin 9, Ireland
Toxicity of Organogermanium CompoundsE. LukevicsLatvian Institute of Organic Synthesis, Riga, LatviaLV 1006
Structural Aspects of Compounds Containing C−E (E=Ge, Sn, Pb) BondsKenneth M. MackayUniversity of Waikato, School of Science and Technology, Hamilton, New Zealand 3105
Safety and Environmental EffectsShigeru MaedaFaculty of Engineering, Kagoshima University, Department of Applied Chemistry and ChemicalEngineering, 1-21-40 Korimoto, Kagoshima, Japan 890
Stereochemistry and Conformation of Organogermanium, Organotin and Organolead CompoundsJames A. MarshallUniversity of South Carolina, Department of Chemistry and Biochemistry, Columbia, SC 29208, USA
ThermochemistryJose A. Martinho SimoesDepartmento de Quımica, Faculdade de Ciencias, Universidade de Lisboa, 1700 Lisboa, Portugal
The Electrochemistry of Alkyl Compounds of Germanium, Tin and LeadMichael MichmanThe Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904
Acidity, Complexing, Basicity and H-Bonding of Organic Germanium, Tin and Lead Compounds:Experimental and Computational ResultsAxel SchulzTechnische Universitat Berlin, Institut fur Anorganische und Analytische Chemie, Strasse des 17. Juni 135,Berlin, Germany D-10623
Organotin ToxicologyLarry R. ShermanUniversity of Scranton, Department of Chemistry, Scranton, PA 18510 4626, USA
127
ThermochemistrySuzanne W. SlaydenDepartment of Chemistry, George Mason University, 4400 University Drive, Fairfax, VA 22030-4444, USA
Photoelectron Spectroscopy (PES) of Organometallic Compounds with C−M (M=Ge, Sn, Pb) BondsStefano StrangesUniversita di Roma ‘La Sapienza’, Dipartimento di Chimica, Piazzale Aldo Moro, 5, Rome, Italy 00185
Synthesis of M(IV) Organometallic Compounds, where M=Ge, Sn, PbJohn M. TsangarisUniversity of Ioannina, Department of Chemistry, Ioannina, Greece GR-45100
The Environmental Methylation of Germanium, Tin and LeadJ. T. Van ElterenDe Montfort University, Department of Chemistry, The Gateway, Leicester, UKLE1 9BH
Syntheses and Uses of Isotopically Labelled Organic Derivatives of Ge, Sn and PbKenneth C WestawayLaurentian University, Department of Chemistry, Sudbury, Ontario, Canada P3E 2C6
Synthesis of M(IV) Organometallic Compounds, where M=Ge, Sn, PbRudolph WillemFree University of Brussels, Pleinlaan 2, Brussels, Belgium B-1050
Analytical Aspects of Organogermanium Compounds
Analytical Aspects of Organolead Compounds
Analytical Aspects of Organotin CompoundsJacob ZabickyInstitutes for Applied Research, Ben-Gurion University of the Negev, Beer-Sheva, Israel 84110
The Chemistry of Amino, Nitroso, Nitro and Related Groups (1996)Edited by Saul Patai
Molecular Mechanics CalculationsPinchas ApedBar-Ilan University, Department of Chemistry, Israel 52900; Ramat-Gan
Analytical Aspects of Amino, Quaternary Ammonium, Nitro, Nitroso and Related FunctionalGroupsShmuel BittnerBen-Gurion University of the Negev, Institutes for Applied Research, Department of Chemistry,Beer-Sheva, Israel
The Chemistry of Ionized, Protonated and Cationated Amines in the Gas PhaseRichard D. BowenUniversity of Bradford, Chemistry and Chemical Technology, Bradford, West Yorkshire, England, UK BD71DP
128
Advances in the Chemistry of Amino and Nitro CompoundsG. V. BoydThe Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904
Acidity and BasicitySilvia BradamanteUniversita di Milano, CNR, Centro di studio sulla Sintesi e Stereochimica di Speciali Sistemi Organici,c/o Dipartimento di Chimica Organica e Industriale, via Golgi 19, Milano, Italia 20133
ThermochemistryMary Stinecipher CampbellLos Alamos National Laboratory, DX-2 Explosive Science Technology, MS C920, Los Alamos, NM87545-0000, USA
Mass Spectrometry of Nitro and Nitroso CompoundsLars CarlsenDepartment of Environmental Chemistry, National Environmental Research Institute, Roskilde, DenmarkDK-4000
Environmental Aspects of Compounds Containing Nitro, Nitroso and Amino GroupsH. K. ChaggerUniversity of Leeds, Department of Fuel and Energy, Leeds, UK LS29JT
Photochemistry of Amines and Amino Compounds
Photochemistry of Nitro and Nitroso CompoundsYuan L. ChowSimonFraser University, Department of Chemistry, Burnaby, British Columbia, Canada V5A 1S6
Mass Spectrometry of Nitro and Nitroso CompoundsHelge EgsgaardRisø; National Laboratory, Environmental Science and Technology Department, Roskilde, DenmarkDK-4000
Reactions of Nitrosoarenes with SH GroupsP. EyerLudwig-Maximilians-Universitat Munchen, Walther-Straub-Institut fur Pharmakologie und Toxikologie,Nuβbaumstr. 26, Munchen, Germany D-80336
Hydrogen Bonding and Complex Formation Involving Compounds with Amino, Nitroso and NitroGroupsLuciano ForlaniDipartimento di Chimica Organica ‘A. Mangini’, viale Risorgimento 4, Bologna, Italy 40136 -
The Electrochemistry of Nitro, Nitroso, and Related CompoundsAlbert J. FryWesleyan University, Middletown, CT, USA
Reactions of Nitrosoarenes with SH GroupsD. GallemannLudwig-Maximilians-Universitat Munchen, Walther-Straub-Institut fur Pharmakologie und Toxikologie,Nuβbaumstr. 26, Munchen, Germany D-80336
129
Photochemistry of Amines and Amino Compounds
Photochemistry of Nitro and Nitroso CompoundsTong-Ing HoNational Taiwan University, Department of Chemistry, Roosevelt Road Section 4, Taipei, Taiwan (ROC)
Radiation Chemistry of Amines, Nitro and Nitroso CompoundsWilliam M HorspoolThe University of Dundee, Department of Chemistry, Dundee, Scotland DD1 4HN
ThermochemistryJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 5401 WilkensAvenue, Baltimore, MA 21228-5398, USA
Nitric Oxide from Arginine: A Biological SurpriseAlan H. MehlerHoward University, Department of Biochemistry and Molecular Biology, Washington, DC, USA
NMR of Compounds Containing—NH2,—NO2 and—NO GroupsChristiana A. MitsopoulouUniversity of Athens, Department of Chemistry, Athens, Greece 15771
SNAr Reactions of Amines in Aprotic SolventsNorma S. NudelmanUniversidad de Buenos Aires, Ciudad Universitaria, Facultad de Ciencias Exactas y Naturales, 1428Buenos Aires, Argentina
Photoelectron Spectra of Amines, Nitroso and Nitro CompoundsPaul RademacherInstitut fur Organische Chemie der Universitat Essen, D-45117 Essen, Germany
NMR of Compounds Containing—NH2,—NO2 and—NO GroupsEdward W. RandallQueen Mary and WestfieldCollege, Department of Chemistry, London, UK
Displacement and ipso-Substitution in NitrationJ. P. B. SandallUniversity of Exeter, Department of Chemistry, Stocker Road, Exeter, UK EX4 4QD
Molecular Mechanics CalculationsHanoch SenderowitzColumbia University, Department of Chemistry, New York, NY 10027, USA
Electronic Effects of Nitro, Nitroso, Amino and Related GroupsJohn ShorterUniversity of Hull, School of Chemistry, Hull, UK HU6 7RX
ThermochemistrySuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA
130
Chiroptical Properties of Amino CompoundsHoward E. SmithVanderbilt University, Department of Chemistry, Nashville, TN 37235, USA
Structural ChemistrySalvatore SorrisoUniversita di Perugia, Dipartimento di Chimica, Laboratorio di Chimica Fisica, Perugia, Italy 06100
The Synthesis and Uses of Isotopically Labelled Amino and Quaternary Ammonium SaltsKenneth C. WestawayLaurentian University, Department of Chemistry, Sudbury, Ontario, Canada P3E 2C6
Environmental Aspects of Compounds Containing Nitro, Nitroso and Amino GroupsA. WilliamsUniversity of Leeds, Department of Fuel and Energy, Leeds, UK LS29JT
Rearrangement Reactions Involving the Amino, Nitro and Nitroso Groups
S- Nitroso Compounds, Formation, Reactions and Biological ActivityD. Lyn H. WilliamsUniversity of Durham, Chemistry Department, Durham, UK
Analytical Aspects of Amino, Quaternary Ammonium, Nitro, Nitroso and Related FunctionalGroupsJacob ZabickyBen-Gurion University of the Negev, Institutes for Applied Research, Department of Chemistry,Beer-Sheva, Israel
Diazotization of Amines and Dediazoniation of Diazonium IonsHeinrich ZollingerTechnisch-Chemisches Laboratorium, Eidgenossische Technische Hochschule (ETH), Zurich, Switzerland
The Chemistry of Organophosphorus Compounds (1996) (See Volume 1 in 1990, Volume 2 in1992, Volume 3 in 1993, Volume 4 in 1996)
Edited by Frank R. Hartley
The Chemistry of Organophosphorus Chemical Warfare AgentsR. M. BlackPorton Down, Chemical and Biological Defence Establishment, Wiltshire, Salisbury, UK SP4 OJQ
Acylphosphonates and their DerivativesEli BreuerThe Hebrew University of Jerusalem, The School of Pharmacy, Department of Pharmaceutical Chemistry,PO Box 12065, Jerusalem, Israel 91120
The Preparation and Properties of Tervalent Phosphorus Acid DerivativesO DahlUniversity of Copenhagen, Department of Chemistry, The H. C. Ørsted Institute, Universitetsparken 5,Copenhagen, Denmark DK-2100
131
Properties and Reactions of Phosphonic and Phosphinic Acids and their Derivatives
The Synthesis of Functionalized Phosphinic and Phosphonic Acids and their Derivatives. Part A:Halo, Hydroxy, Epoxy, Mercapto, Carboxy and Oxo Functionalized Acids
The Synthesis of Functionalized Phosphinic and Phosphonic Acids and their Derivatives. Part B:Diazo, Nitro and Amino Functionalized Acids
The Synthesis of Phosphonic and Phosphinic Acids and their Derivatives: Non-Functionalized Acids
The Synthesis and Reactions of Thio- and Seleno-Phosphonic and -Phosphinic AcidsR. S. EdmundsonWentworth Avenue, Leeds, UKLS17 7TN
The Chemistry of Organophosphorus Chemical Warfare AgentsJ. M. HarrisonPorton Down, Chemical and Biological Defence Establishment, Wiltshire, Salisbury, UKSP4 OJQ
Biological Activity of Phosphonic and Phosphinic AcidsAsher KalirTelAviv University, Department of Physiology and Pharmacology, Sackler Faculty of Medicine, Tel Aviv,Israel 69978
Biological Activity of Phosphonic and Phosphinic AcidsHenry H. KalirUniversity of Medicine and Dentistry of New Jersey, Department of Psychiatry, New Jersey MedicalSchool, University Heights, Newark, NJ 07103-2714, USA
Gas-Phase Positive and Negative Ion Chemistry of Organophosphorus Compounds via MassSpectrometric TechniquesRichard A. J. O’HairKansas State University, Department of Chemistry, Willard Hall, Manhattan, KS 66506-3701, USA
The Chemistry of Dienes and Polyenes (1997) (See Volume 2 in 2000)
Edited by Zvi Rappoport
Analysis of Dienes and Polyenes and Their Structure DeterminationZeev AizenshtatThe Hebrew University of Jerusalem, Jerusalem, Casali Institute for Applied Chemistry and Department ofOrganic Chemistry, Jerusalem, Israel 91904
Radiation Chemistry of Dienes and PolyenesZeev B. AlfassiBenGurion University, Department of Nuclear Engineering, Beer Sheva, Israel 84102
Palladium-Catalyzed Oxidation of DienesJan-E. BackvallUniversity of Uppsala, Department of Organic Chemistry, Box 531, Uppsala, Sweden S-751 21
Electronic Structure of Diene and Polyene Radical CationsThomas BallyUniversite de Fribourg, Institut de Chimie Physique, Perolles, Fribourg, Switzerland CH-1700
132
Conformation and Chiroptical Properties of Dienes and PolyenesLorenzo d i BariCentro di Studio del CNR per le Macromolecole Stereoordinate ed Otticamente Attive, Dipartimento diChimica e Chimica Industriale, Via Risorgimento 35, Pisa, Italy I-56126
Structural Chemistry of Dienes and PolyenesJordi Benet-BuchholzUniversitat Essen, Institut fur Anorganische Chemie, Universitatsstrasse 3–5, Essen, Germany D-45117
Contribution of Quantum Chemistry to the Study of Dienes and PolyenesJ. BertranUniversitat Autonoma de Barcelona, Departament de Quımica, Bellaterra, Spain 08193
Structural Chemistry of Dienes and PolyenesRoland BoeseUniversitat Essen, Institut fur Anorganische Chemie, Universitatsstrasse 3–5, Essen, Germany D-45117
Intramolecular Cyclization of Dienes and PolyenesGerhard V. BoydThe Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904
Contribution of Quantum Chemistry to the Study of Dienes and PolyenesV. BranchadellUniversitat Autonoma de Barcelona, Departament de Quımica, Bellaterra, Spain 08193
Structural Effects on Dienes and PolyenesMarvin ChartonSchoolof Liberal Arts and Sciences, Chemistry Department, Pratt Institute, Brooklyn, NY11205, USA
The Effect of Pressure on Reactions of Dienes and PolyenesMatthias K. DiedrichUniversitat Gesamthochschule Essen, Institut fur Organische Chemie, Essen, Germany D-45117
Ultraviolet/Visible, Infrared and Raman SpectraYukio FurukawaDepartment of Chemistry, School of Science, The University of Tokyo, Bunkyo-ku Tokyo, Japan 113
Structural Chemistry of Dienes and PolyenesThomas HaumannUniversitat Essen, Institut fur Anorganische Chemie, Universitatsstrasse 3–5, Essen, Germany D-45117
Electronic Structure of Diene and Polyene Radical CationsEdgar HeilbronnerGrutstrasse 10, Herrliberg, Switzerland CH-8704
Synthesis and Transformation of RadialenesHenning HopfTechnical University of Braunschweig, Institut fur Organische Chemie, Hagenring 30, Braunschweig,Germany D-38106
Syntheses and Uses of Isotopically Labelled Dienes and PolyenesMarianna KanskaUniversity of Warsaw, Department of Chemistry, Poland
133
The Electrochemistry of Dienes and PolyenesShigenori KashimuraKin-ki University, Higashi-Osaka, Japan 577
Oxidation of Dienes and PolyenesAlexander M. KhenkinThe Hebrew University of Jerusalem, Casali Institute of Applied Chemistry, Graduate School of AppliedScience, Jerusalem, Israel 91904
Acidity of Alkenes and PolyenesKathleen V. KilwayUniversity of California, Department of Chemistry, 94720-1460, Berkeley, CA, USA
The Electrochemistry of Dienes and PolyenesNaoki KiseTottori University, Tottori, Japan 680
The Effect of Pressure on Reactions of Dienes and PolyenesFrank-Gerrit KlarnerUniversitat Gesamthochschule Essen, Institut fur Organische Chemie, Essen, Germany D-45117
ThermochemistryJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry,, 1000 HilltopCircle, Baltimore, MD 21250, USA
Synthesis and Transformation of RadialenesGerhard MaasUniversity of Ulm, Abteilung Organische Chemie I, Albert-Einstein-Allee 11, Ulm, Germany D-89069
Synthesis of Conjugated Dienes and PolyenesGoverdhan MehtaUniversity of Hyderabad, Molecular Design and Synthesis Unit of JNCASR and School of Chemistry,Hyderabad, India 500 046
Oxidation of Dienes and PolyenesRonny NeumannThe Hebrew University of Jerusalem, Casali Institute of Applied Chemistry, Graduate School of AppliedScience, Jerusalem, Israel 91904
The Photochemistry of Dienes and Polyenes: Application to the Synthesis of Complex MoleculesJohn M. NussChiron Corporation, 4560 Horton Street, Emeryville, CA 94608, USA
Contribution of Quantum Chemistry to the Study of Dienes and PolyenesA. OlivaUniversitat Autonoma de Barcelona, Departament de Quımica, Bellaterra, Spain 08193
Synthesis of Conjugated Dienes and PolyenesH. Surya Prakash RaoPondicherry University, Department of Chemistry, Pondicherry, India 605 014
134
Conformation and Chiroptical Properties of Dienes and PolyenesCarlo RosiniCentro di Studio del CNR per le Macromolecole Stereoordinate ed Otticamente Attive, Dipartimento diChimica e Chimica Industriale, Via Risorgimento 35, Pisa, Italy I-56126
Conformation and Chiroptical Properties of Dienes and PolyenesPiero SalvadoriCentro di Studio del CNR per le Macromolecole Stereoordinate ed Otticamente Attive, Dipartimento diChimica e Chimica Industriale, Via Risorgimento 35, Pisa, Italy I-56126
The Electrochemistry of Dienes and PolyenesTatsuya ShonoKin-ki University, Higashi-Osaka, Japan 577
Contribution of Quantum Chemistry to the Study of Dienes and PolyenesM. SodupeUniversitat Autonoma de Barcelona, Departament de Quımica, Bellaterra, Spain 08193
Acidity of Alkenes and PolyenesAndrew StreitwieserUniversity of California, Department of Chemistry, 94720-1460, Berkeley, CA, USA
Allenyl and Polyenyl CationsL. R. SubramanianEberhard-Karls-Universitat Tubingen, Institut fur Organische Chemie, Auf der Morgenstelle 18, Tubingen,Germany D-72076
Structural Chemistry of Dienes and PolyenesMarit TraettebergNorwegian University of Science and Technology, Department of Chemistry, Trondheim, Norway N-7055
The Photochemistry of Dienes and Polyenes: Application to the Synthesis of Complex MoleculesFrederick G. WestUniversity of Utah, Salt Lake City, Department of Chemistry, UT, USA 84112
Syntheses and Uses of Isotopically Labelled Dienes and PolyenesMieczysław ZielinskiJagiellonian University, Isotope Laboratory, Faculty of Chemistry, Cracow, Poland
Radical Addition to PolyenesH. ZipseTechnische Universitat Berlin, Institut fur Organische Chemie, Strasse des 17 Juni: 135, Berlin, GermanyD-10623
The Chemistry of Double-bonded Functional Groups (1997)Edited by Saul Patai
The Thiocarbonyl GroupJ.-L. M. AbboudC.S.I.C., Instituto de Quımica Fısica ‘Rocasolano’, Serrano 119, Madrid, Spain E-28006
135
Pyrolysis Involving Compounds with C=C, C=N and C=O Double BondsR. Alan AitkenUniversity of St. Andrews, School of Chemistry, St. Andrews, Fife, UKKY16 9ST
Epoxidation of C=X Double BondsMihaly BartokJozsef Attila University, Department of Organic Chemistry and Organic Catalysis Research Group of theHungarian Academy of Sciences, Dom ter 8, Szeged, Hungary H-6720
Heterogeneous Catalytic HydrogenationMihaly BartokJozsef Attila University, Department of Organic Chemistry and Organic Catalysis Research Group of theHungarian Academy of Sciences, Dom ter 8, Szeged, Hungary H-6720
Heteropolar Double BondsHarold BaschBar-Ilan University, Department of Chemistry, Ramat-Gan, Israel 52900
Radical Anions and Radical Cations Derived from Compounds Containing C=C, C=O or C=NGroupsDaniel J. BergerVirginia Polytechnic Institute and State University, Department of Chemistry, Blacksburg, VA 24061-0212,USA
Chiroptical Properties of Compounds Containing C=O GroupsStefan E. BoiadjievUniversity of Nevada, Department of Chemistry, Reno, NV 89557, USA
Dipole Moments of Compounds Containing Double BondsOtto ExnerAcademy of Sciences of the Czech Republic, Institute of Organic Chemistry and Biochemistry, Prague,Czech Republic
Complex Formation Involving Compounds with Double-Bonded Functional GroupsLuciano ForlaniDipartimento di Chimica Organica ‘A. Mangini’, viale Risorgimento 4, Bologna, Italy 40136
The Electrochemistry of the C=C, C=O and C=N GroupsAlbert J. FryWesleyan University, Middletown, CT, USA
Mass Spectra of Double-Bonded GroupsTino GaumannInstitute of Physical Chemistry, Federal Institute of Technology, Lausanne, Switzerland 1015
The Chiroptical Properties of the Carbon–Carbon Double BondAharon GedankenBar-Ilan University, Ramat-Gan, Israel 52900
Liquid Crystals with X=Y GroupsW. HaaseInstitut fur Physikalische Chemie, Technische Hochschule, Petersenstr. 20, Darmstadt, Germany 64287
136
Photochemistry of Compounds Containing C=C Double BondsNizar HaddadTechnion—Israel Institute of Technology, Department of Chemistry, Haifa, Israel 32000
Liquid Crystals with X=Y GroupsT. HanemannInstitut fur Materialforschung III, Forschungszentrum Karlsruhe, Postfach 3640, Karlsruhe, Germany76021
N-Oxidative Transformations of C=N Groups as Means of Toxification and DetoxificationPeter HlavicaLudwig-Maximilians-Universitat Munchen, Walther-Straub-Institut fur Pharmakologie and Toxikologie,Nussbaumstrasse 26, Munchen, Germany D-80336
Some Synthetic Uses of Double-Bonded Functional GroupsJeff HoyleNova ScotiaAgricultural College, Chemistry and Soil Science Department, Truro, Nova Scotia, CanadaB2N 5E3
Heteropolar Double BondsTova HozBar-Ilan University, Department of Chemistry, Ramat-Gan, Israel 52900
Advances in the Metathesis of OlefinsK. J. IvinThe Queen’s University of Belfast, and 12, St. Michael’s Gardens, South Petherton, Somerset, UK TA135BD
Biological Activity of Organic Compounds Elicited by the Introduction of Double BondsAsher KalirTelAviv University, Department of Physiology and Pharmacology, Sackler Faculty of Medicine, Tel Aviv,Israel 69978
Biological Activity of Organic Compounds Elicited by the Introduction of Double BondsHenry H. KalirDepartment of Histology and Cell Biology, Sackler Faculty of Medicine, Tel Aviv, Israel 69978 and IchilovHospital, Department of Psychiatry
Syntheses and Uses of Isotopically Labelled Compounds Containing C=C, C=O or C=N GroupsMarianna KanskaWarsaw University, Department of Chemistry, Warsaw, Poland
Acidity, Basicity and H-Bonding of Double-Bonded Functional Groups: Nitrones, Nitriles andThiocarbonylsThomas M. KlapotkeUniversity of Glasgow, Department of Chemistry, University Avenue, Glasgow, UK G12 8QQ
Electrophilic Additions to Double BondsPavel KocovskyUniversity of Leicester, Department of Chemistry, Leicester, UK LE1 7RH
137
N-Oxidative Transformations of C=N Groups as Means of Toxification and DetoxificationMichael LehnererLudwig-Maximilians-Universitat Munchen, Walther-Straub-Institut fur Pharmakologie and Toxikologie,Nussbaumstrasse 26, Munchen, Germany D-80336
ThermochemistryJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
Chiroptical Properties of Compounds Containing C=O GroupsDavid A. LightnerUniversity of Nevada, Department of Chemistry, Reno, NV 89557, USA
The Thiocarbonyl GroupO. MoUniversidad Autonoma de Madrid, Departamento de Quımica, C-9, Cantoblanco, Madrid, Spain E-28049
The Thiocarbonyl GroupM. T. MolinaC.S.I.C., Instituto de Quımica Medica, Juan de la Cierva 3, Madrid, Spain E-28006
Heterogeneous Catalytic HydrogenationArpadMolnarJozsef Attila University, Department of Organic Chemistry and Organic Catalysis Research Group of theHungarian Academy of Sciences, Dom ter 8, Szeged, Hungary H-6720
The Thiocarbonyl GroupR. NotarioC.S.I.C., Instituto de Quımica Fısica ‘Rocasolano’, Serrano 119, Madrid, Spain E-28006
Acidity, Basicity and H-Bonding of Double-Bonded Functional Groups: Nitrones, Nitriles andThiocarbonylsClaudia M. RienackerUniversity of Glasgow, Department of Chemistry, University Avenue, Glasgow, UKG12 8QQ
Strained OlefinsJan SandstromCenter for Chemistry and Chemical Engineering, University of Lund, Division of Organic Chemistry 1,124, Lund, Sweden S-221 00
Epoxidation of C=X Double BondsGyula SchneiderJozsef Attila University, Department of Organic Chemistry, Dom ter 8, Szeged, Hungary H-6720
Electronic Effects of Groups Containing Carbon–Carbon or Carbon–Oxygen Double BondsJohn ShorterUniversity of Hull, School of Chemistry, Hull, UK HU6 7RX
ThermochemistrySuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA
138
Radical Anions and Radical Cations Derived from Compounds Containing C=C, C=O or C=NGroupsJames M. TankoVirginia Polytechnic Institute and State University, Department of Chemistry, Blacksburg, VA 24061-0212,USA
Nucleophilic Attack on Compounds Containing C=C, C=O or C=N GroupsPeter G. TaylorOpen University, Chemistry Department, Walton Hall, Milton Keynes, Bucks, UK MK7 6AA
Pyrolysis Involving Compounds with C=C, C=N and C=O Double BondsAndrew W. ThomasUniversity of St. Andrews, School of Chemistry, St. Andrews, Fife, UK KY16 9ST
Hydrogenation of Compounds Containing C=C, C=O and C=N BondsMartin WillsUniversity of Warwick, Department of Chemistry, Coventry, UK CV4 7AL
The Thiocarbonyl GroupM. YanezUniversidad Autonoma de Madrid, Departamento de Quımica, C-9, Cantoblanco, Madrid, Spain E-28049
Syntheses and Uses of Isotopically Labelled Compounds Containing C=C, C=O or C=N GroupsMieczysław ZiełinskiJagiellonian University, Isotope Laboratory, Faculty of Chemistry, Cracow, Poland; 48-12-34-05-15
The Chemistry of the Hydrazo, Azo and Azoxy Groups (1997) (See Volume 1 in 1975)
Edited by Saul Patai
ThermochemistryHussein Y. AfeefyUniversity of MarylandBaltimoreCounty, 1000 Hilltop Circle, Baltimore, MD 21250, USA
Radiation Chemistry of Azo and Hydrazo CompoundsZeev B. AlfassiBenGurion University of the Negev, Department of Nuclear Engineering, Beer Sheva 84102, Israel
Radical Reactions of Azo, Hydrazo and Azoxy CompoundsJ.-P AnselmeUniversity of Massachusetts at Boston, Boston, MA 02125-3393, USA
Biological Formation and Reactions of Hydrazo, Azo and Azoxy GroupsDerek V. BanthorpeUniversity College London, Chemistry Department, London, UK
Electronic Structure of Hydrazo, Azo and Azoxy CompoundsHarold BaschBar Ilan University, Department of Chemistry, Ramat Gan52900, Israel
Synthesis and Reactions of Hydrazo, Azo and Azoxy CompoundsGerhard V. BoydThe Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904
139
Rearrangements of Hydrazo, Azoxy and Azo Compounds: Kinetic, Product and Isotope StudiesErwin BuncelQueen’s University, Department of Chemistry, Kingston, Ontario, Canada K7L 3N6
Configuration, Conformation and Chiroptical Properties of the Azo, Azoxy and Hydrazo GroupsOtakar CervinkaInstituteof Chemical Technology, Department of Organic Chemistry, 166 28 Prague 6, Czech Republic
Mass Spectra of Hydrazo, Azo and Azoxy CompoundsT.-W.D. ChanThe Chinese University of Hong Kong, Department of Chemistry, Shatin, N.T., Hong Kong
Rearrangements of Hydrazo, Azoxy and Azo Compounds: Kinetic, Product and Isotope StudiesRobin A. COXUniversity of Toronto, Department of Chemistry, Toronto, Ontario, Canada M5S 3H6
Safety and Environmental Effects of Azo CompoundsVictor GlezerThe Hebrew University of Jerusalem, Division of Environmental Sciences, Fredy and Nadine HerrmannSchool of Applied Science, Jerusalem, Israel 91904
Analytical Aspects of Compounds Containing the Azo, Azoxy and Hydrazino Functional GroupsSarina GrinbergBen-Gurion University of the Negev, Institutes for Applied Research, Beer-Sheva, Israel 84105
Cathodic and Anodic Behaviour of Organic Compounds Possessing −N=N− or >N−N< LinkagesNoe lle Gueguen-simonetUniversite de Rennes 1, Laboratoire d’Electrochimie moleculaire et macromoleculaire, UMR N◦ 6510,Campus de Beaulieu, France
The Photochemistry of the Hydrazo, Azo and Azoxy GroupsWilliam M. HorspoolThe University of Dundee, Department of Chemistry, Dundee, Scotland, UK DD1 4HN
Electronic Structure of Hydrazo, Azo and Azoxy CompoundsTova HozBar Ilan University, Department of Chemistry, Ramat Gan52900, Israel
Acidity, Basicity and Complex FormationThomas M KlapotkeUniversity of Glasgow, Department of Chemistry, Glasgow, UK G12 8QQ
Radical Reactions of Azo, Hydrazo and Azoxy CompoundsGen KogaIbaraki University, Mito, Japan 310
The Photoelectron Spectroscopy of Hydrazo, Azo and Azoxy CompoundsBranka Kovac‘Rugjer Boskovic’ Institute, Physical Chemistry Division, Zagreb, Croatia 10000
ThermochemistryJoel F. LiebmanUniversity of Maryland Baltimore Country, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
140
NMR Spectroscopy of Azo, Azoxy and Hydrazo CompoundsJoan MasonThe Open University, Department of Chemistry, Milton Keynes, UK MK7 6AA
Information from the ESR, ENDOR and NMR Spectra of Radicals Related to Hydrazo, Azo andAzoxy CompoundsS.F. NelsenUniversity of Wisconsin, Madison, Department of Chemistry, 1101 University Avenue, Madison, WI53706-1396, USA
Toxicological and Pharmacotherapeutical Aspects of Azo, Hydrazo and Azoxy CompoundsIsaac NirThe Hebrew University of Jerusalem, Department of Pharmacology, Faculty of Medicine, Jerusalem, Israel
The Photoelectron Spectroscopy of Hydrazo, Azo and Azoxy CompoundsIgor NovakNational University of Singapore, Department of Chemistry, Singapore, Singapore 119260
Electronic Effects of Hydrazo, Azo and Azoxy GroupsJohn ShorterUniversity of Hull, School of Chemistry, Hull, UK HU6 7RX
Cathodic and Anodic Behaviour of Organic Compounds Possessing −N=N− or >N−N< LinkagesJacques SimonetUniversite de Rennes 1, Laboratoire d’Electrochimie moleculaire et macromoleculaire, UMR N◦ 6510,Campus de Beaulieu, France
ThermochemistrySuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA
Mass Spectra of Hydrazo, Azo and Azoxy CompoundsS.W. TamThe Open Learning Institute of Hong Kong, Homantin, Kowloon, Hong Kong
Radical Reactions of Azo, Hydrazo and Azoxy CompoundsJohn C. WarnerUniversity of Massachusetts at Boston, Boston, MA 02125-3393, USA
Analytical Aspects of Compounds Containing the Azo, Azoxy and Hydrazino Functional GroupsJacob ZabickyBen-Gurion University of the Negev, Institutes for Applied Research, Beer-Sheva, Israel 84105
The Chemistry of Organic Silicon Compounds, Volume 2 (1998) (See Volume 1 in 1989,Volume 3 in 2001)
Edited by Zvi Rappoport and Yitzhak Apeloig
Cyclic Polychalcogenide Compounds with Silicon
Highly Reactive Small-Ring Monosilacycles and Medium-Ring Oligosilacycles
141
Organosilicon Derivatives of FullerenesWataru AndoUniversity of Tsukuba, Department of Chemistry, Ibaraki 305, Tsukuba, Japan
Theoretical Aspects and Quantum Mechanical Calculations of Silaaromatic CompoundsYitzhak ApeloigTechnion—Israel Institute of Technology, Department of Chemistry and the LiseMeitner-MinervaCenterfor Computational Quantum Chemistry, Haifa, Israel 32000
Silicon–Carbon and Silicon–Nitrogen Multiply Bonded CompoundsNorbert AunerFachinstitut fur Anorganische und Allgemeine Chemie der Humboldt Universitat Berlin, Berlin, FRG D10115
Organo-Silica Sol–Gel MaterialsDavid AvnirThe Hebrew University of Jerusalem, Institute of Chemistry, Jerusalem, Israel 91904
Activating and Directive Effects of Silicon
Reaction Mechanisms of Nucleophilic Attack at SiliconAlan R. BassindaleThe Open University, Department of Chemistry, Milton Keynes, UKMK7 6AA
ThermochemistryRosa BecerraCSIC, Instituto de Quimica Fisica ‘Rocasolano’, C/Serrano, 119, Madrid, Spain 28006
Alkaline and Alkaline Earth Silyl Compounds—Preparation and StructureJohannes BelznerInstitut fur Organische Chemie der Georg-August-Universitat Gottingen, Tammannstr., Gottingen,Germany 2, D-37077
A Molecular Modeling of the Bonded Interactions of Crystalline SilicaM. B. Boisen JrMaterials Science and Engineering and Mathematics, Departments of Geological Sciences, Virginia Tech,Blacksburg, VA 24061, USA
The Structural Chemistry of Organosilicon CompoundsMark BotoshanskyTechnion–Israel Institute of Technology, Department of Chemistry, Haifa, Israel 32000
The Photochemistry of Organosilicon CompoundsA. G. BrookUniversity of Toronto, Lash Miller Chemical Laboratories, Toronto, Ontario, Canada M5S 3H6
Acyl SilanesPhilip C. Bulman PageLoughborough University, Department of Chemistry, Loughborough, Leicestershire, UK LE11 3TU
Tris(trimethylsilyl)silane in Organic SynthesisC. ChatgilialogluConsiglio Nazionale delle Ricerche, I.Co.C.E.A., Via P. Gobetti 101, Bologna, Italy 40129
142
Steric Effects of Silyl GroupsBuh-Luen ChengInstituteof Chemistry, Organosilicon and Synthesis Laboratory, Academia Sinica, Nankang, Taipei,Taiwan, Peoples’ Republic of China 11529 andNational TsingHua University, Department of Chemistry, Hsinchu, Taiwan, Peoples’ Republic of China30043
Cyclic Polychalcogenide Compounds with SiliconNami ChoiUniversity of Tsukuba, Department of Chemistry, Tsukuba, JapanIbaraki 305
Recent Synthetic Applications of Organosilicon ReagentsErnest W. ColvinUniversity of Glasgow, Department of Chemistry, G12 8QQ, Glasgow, UK
Alkaline and Alkaline Earth Silyl Compounds—Preparation and StructureUwe DehnertInstitut fur Organische Chemie der Georg-August-Universitat Gottingen, Tammannstr., Gottingen,Germany 2, D-37077
Recent Advances in the Chemistry of Siloxane Polymers and CopolymersRobert DrakeDow Corning Ltd, Cardiff Road, Barry, South Glamorgan, UKCF63 2YL
Group 14 Metalloles, Ionic Species and Coordination CompoundsJacques DubacUniversite Paul-Sabatier, Heterochimie Fondamentale et Appliquee (ESA-CNRS 5069), 118, Route deNarbonne, ToulouseCedex, France 31062
Transition-Metal Silyl ComplexesMoris S. EisenTechnion—Israel Institute of Technology, Department of Chemistry, Kiryat Hatechnion, Haifa, Israel32000
Tris(trimethylsilyl)silane in Organic SynthesisC. FerreriConsiglio Nazionale delle Ricerche, I.Co.C.E.A., Via P. Gobetti 101, Bologna, Italy 40129
Chemistry of Compounds with Silicon–Sulphur, Silicon–Selenium and Silicon–Tellurium BondsD. A. (‘Fred’) ArmitageKing’s College London, Department of Chemistry, Strand, London, UKWC2R 2LS
Electrochemistry of Organosilicon CompoundsToshio FuchigamiTokyo Institute of Technology, Department of Electrochemistry, Midori-ku, Yokohama, Japan 226
SilylenesPeter P GasparWashington University, Department of Chemistry, St. Louis, MI 63130-4899, USA
A Molecular Modeling of the Bonded Interactions of Crystalline SilicaG. V. GibbsMaterials Science and Engineering and Mathematics, Departments of Geological Sciences, Virginia Tech,Blacksburg, VA 24061, USA
143
Tris(trimethylsilyl)silane in Organic SynthesisT. GimisisConsiglio Nazionale delle Ricerche, I.Co.C.E.A., Via P. Gobetti 101, Bologna, Italy 40129
Activating and Directive Effects of Silicon
Reaction Mechanisms of Nucleophilic Attack at SiliconSimon J. GlynnThe Open University, Department of Chemistry, Milton Keynes, UKMK7 6AA
Gas-Phase Ion Chemistry of Silicon-Containing MoleculesNorman GoldbergInstitut fur Organische Chemie der Technischen Universitat Berlin, Straße des 17 Juni 135, Berlin,Germany D-10623
Group 14 Metalloles, Ionic Species and Coordination CompoundsChristian GuerinUniversite Montpellier II, Chimie Moleculaire et Organisation du Solide (UMR-CNRS 5637), Place E.Bataillon, Montpellier Cedex 5, France 34095
Recent Advances in the Chemistry of CyclopolysilanesEdwin HenggeTechnical University, Institute of Inorganic Chemistry, Graz, Austria
Steric Effects of Silyl GroupsR. Jih-Ru HwuInstitute of Chemistry, Organosilicon and Synthesis Laboratory, Academia Sinica, Nankang, Taipei,Taiwan, Peoples’ Republic of China 11529 andNational TsingHua University, Department of Chemistry, Hsinchu, Taiwan, Peoples’ Republic of China30043
Matrix Isolation Studies of Silicon CompoundsJorg JungInstitut fur Organische Chemie der Justus-Liebig-Universitat Giessen, Heinrich-Buff-Ring 58, Giessen,Federal Republic of Germany D-35392
Cyclopentadienyl Silicon CompoundsPeter JutziUniversity of Bielefeld, Faculty of Chemistry, Bielefeld, Germany 33615
Highly Reactive Small-Ring Monosilacycles and Medium-Ring OligosilacyclesYoshio KabeUniversity of Tsukuba, Department of Chemistry, Ibaraki 305, Tsukuba, Japan
The Structural Chemistry of Organosilicon CompoundsMenahem KaftoryTechnion–Israel Institute of Technology, Department of Chemistry, Haifa, Israel 32000
Hypervalent Silicon CompoundsInna KalikhmanBen-Gurion University of the Negev, Department of Chemistry, Beer Sheva, Israel 84105
144
The Structural Chemistry of Organosilicon CompoundsMoshe KaponTechnion–Israel Institute of Technology, Department of Chemistry, Haifa, Israel 32000
Theoretical Aspects and Quantum Mechanical Calculations of Silaaromatic CompoundsMiriam KarniTechnion—Israel Institute of Technology, Department of Chemistry and the LiseMeitner-MinervaCenterfor Computational Quantum Chemistry, Haifa, Israel 32000
Mechanistic Aspects of the Photochemistry of Organosilicon CompoundsMitsuo KiraTohoku University, Graduate School of Science, Department of Chemistry, Aoba-ku, Sendai, Japan 980-77
Silatranes and their Tricyclic AnalogsSvetlana KirpichenkoSiberian Branch of the Russian Academy of Sciences, Irkutsk Institute of Chemistry, 1 Favorsky St, Irkutsk,Russia 664033
Acyl SilanesSukhbinder S. KlairLoughborough University, Department of Chemistry, Loughborough, Leicestershire, UKLE11 3TU
Organo-Silica Sol–Gel MaterialsLisa C. KleinRutgers—The State University of New Jersey, Ceramics Department, Piscataway, NJ 08855-0909, USA
Tautomeric Equilibria and Rearrangements Involving PhenolsAlla V. KoblikChemBridge Corporation, Malaya Pirogovskaya str., 1, Moscow, Russia 119435
Hypervalent Silicon CompoundsDaniel KostBen-Gurion University of the Negev, Department of Chemistry, Beer Sheva, Israel 84105
Organosilicon Derivatives of FullerenesTakahiro KusukawaUniversity of Tsukuba, Department of Chemistry, Tsukuba, Ibaraki, Japan 305
Si-Containing Ceramic PrecursorsR. M. LaineUniversity of Michigan, Departments of Materials Science and Engineering and Chemistry, Ann Arbor, MI48109-2136, USA
Organo-Silica Sol–Gel MaterialsDavid LevyInstituto de Ciencia de Materiales de Madrid, C.S.I.C., Cantoblanco, Madrid, Spain 28049
Recent Advances in the Direct ProcessLarry N. LewisGE Corporate Research & DevelopmentCenter, Schenectady, NY, USA 12309
Recent Advances in the Hydrosilylation and Related ReactionsZhaoyang LiState University of New York at Stony Brook, Department of Chemistry, Stony Brook, NY 11794-3400, USA
145
Silicenium Ions—Experimental AspectsPaul D. LickissImperial College of Science, Department of Chemistry, Technology and Medicine, London, UK SW7 2AY
Synthetic Applications of Allylsilanes and VinylsilanesShiuh-Tzung LiuNationalTaiwan University, Department of Chemistry, Taipei, Taiwan, Peoples’ Republic of China 106
Synthetic Applications of Allylsilanes and VinylsilanesTien-Yau LuhNational Taiwan University, Department of Chemistry, Taipei, Taiwan, Peoples’ Republic of China 106
Tautomeric Equilibria and Rearrangements Involving PhenolsSergei M. LukyanovChemBridge Corporation, Malaya Pirogovskaya str., 1, Moscow, Russia 119435
Silicon-Substituted CarbenesGerhard MaasUniversitat Ulm, Abteilung Organische Chemie I, Albert-Einstein-Allee 11, Ulm, Germany D-89081
Recent Advances in the Chemistry of Siloxane Polymers and CopolymersIain MacKinnonDow Corning Ltd, Cardiff Road, Barry, South Glamorgan, UKCF63 2YL
Silicenium Ions: Quantum Chemical ComputationsChristoph MaerkerThe University of Erlangen-Nurnberg, Computer Chemistry Center of the Institute of Organic Chemistry,Henkestrasse 42, Erlangen, Germany 91054
Matrix Isolation Studies of Silicon CompoundsGunther MaierInstitut fur Organische Chemie der Justus-Liebig-Universitat Giessen, Heinrich-Buff-Ring 58, Giessen,Federal Republic of Germany D-35392
Acyl SilanesMichael J. MckenzieLoughborough University, Department of Chemistry, Loughborough, Leicestershire, UKLE11 3TU
Matrix Isolation Studies of Silicon CompoundsAndreas MeudtInstitut fur Organische Chemie der Justus-Liebig-Universitat Giessen, Heinrich-Buff-Ring 58, Giessen,Federal Republic of Germany D-35392
Group 14 Metalloles, Ionic Species and Coordination CompoundsPhilippe MeunierUniversite de Bourgogne, Synthese et Electrosynthese Organometalliques (UMR-CNRS 5632), 6 BoulevardGabriel, DijonCedex, France 21004
Mechanistic Aspects of the Photochemistry of Organosilicon CompoundsTakashi MiyazawaThe Institute of Physical and Chemical Research, PhotodynamicsResearchCenter, (RIKEN), 19-1399,Koeji, Nagamachi, Aoba-ku, Sendai, Japan 980
146
Silicon–Carbon and Silicon–Nitrogen Multiply Bonded Compounds
Silyl-Substituted CarbocationsThomas MullerHumboldt Universitat Berlin, Fachinstitut fur Anorganische und Analytische Chemie der, Berlin, GermanyD-10115
Polyhedral Silicon CompoundsShigeru NagaseTokyo Metropolitan University, Department of Chemistry, Graduate School of Science, Tokyo, Hachioji,Japan 192-03
Recent Advances in the Hydrosilylation and Related ReactionsIwao OjimaState University of New York at Stony Brook, Department of Chemistry, Stony Brook, NY 11794-3400, USA
Recent Advances in the Chemistry of Silicon–Heteroatom Multiple BondsRenji OkazakiThe University of Tokyo, Department of Chemistry, Graduate School of Science, 7-3-1 Hongo, Bunkyo-ku,Tokyo, Japan 113
Matrix Isolation Studies of Silicon CompoundsHarald PaclInstitut fur Organische Chemie der Justus-Liebig-Universitat Giessen, Heinrich-Buff-Ring 58, Giessen,Federal Republic of Germany D-35392
Silatranes and their Tricyclic AnalogsVadim PestunovichSiberian Branch of the Russian Academy of Sciences, Irkutsk Institute of Chemistry, 1 Favorsky St, Irkutsk,Russia 664033
Silicenium Ions: Quantum Chemical ComputationsPaul von Rague SchleyerThe University of Erlangen-Nurnberg, Computer Chemistry Center of the Institute of Organic Chemistry,Henkestrasse 42, Erlangen, Germany 91054
Acyl SilanesStephen RosenthalLoughborough University, Department of Chemistry, Loughborough, Leicestershire, UKLE11 3TU
Mechanism and Structures in Alcohol Addition Reactions of Disilenes and SilenesHideki SakuraiScience University of Tokyo, Department of Industrial Chemistry, Faculty of Science and Technology,Noda, Chiba, Japan 278
Organo-Silica Sol–Gel MaterialsUlrich Schubertthe Technical University of Vienna, Institute for Inorganic Chemistry, Vienna, Austria A-1060
Gas-Phase Ion Chemistry of Silicon-Containing MoleculesHelmut SchwarzInstitut fur Organische Chemie der Technischen Universitat Berlin, Straße des 17 Juni 135, Berlin,Germany D-10623
147
Polyhedral Silicon CompoundsAkira SekiguchiUniversity of Tsukuba, Department of Chemistry, Tsukuba, Ibaraki, Japan 305
Si-Containing Ceramic PrecursorsA. SellingerUniversity of New Mexico, Sandia National Laboratory, Advanced Materials Laboratory, 1001 UniversityBlvd. S.E., Albuquerque, NM 87106, USA
Silyl-Substituted CarbocationsHans-Ullrich SiehlUniversitat Ulm, Abteilung fur Organische Chemie I der, Ulm, Germany D-86069
Recent Advances in the Chemistry of CyclopolysilanesHarald StugerTechnical University, Institute of Inorganic Chemistry, Graz, Austria
Chirality in Bioorganosilicon ChemistryReinhold TackeUniversitat Wurzburg, Institut fur Anorganische Chemie, Am Hubland, Wurzburg, Germany D-97074
29Si NMR Spectroscopy of Organosilicon CompoundsToshio TakayamaKanagawa University, Department of Applied Chemistry, Faculty of Engineering, 3-27-1 Rokkakubashi,Yokohama, Japan 221
29Si NMR Spectroscopy of Organosilicon CompoundsYoshito TakeuchiKanagawa University, Department of Chemistry, Faculty of Science, 2946 Tsuchiya, Hiratsuka, Japan259-12
Activating and Directive Effects of Silicon
Reaction Mechanisms of Nucleophilic Attack at SiliconPeter G. TaylorThe Open University, Department of Chemistry, Milton Keynes, UKMK7 6AA
Recent Advances in the Chemistry of Siloxane Polymers and CopolymersRichard TaylorDow Corning Ltd, Cardiff Road, Barry, South Glamorgan, UKCF63 2YL
Recent Advances in the Chemistry of Silicon–Heteroatom Multiple BondsNorihiro TokitohThe University of Tokyo, Department of Chemistry, Graduate School of Science, 7-3-1 Hongo, Bunkyo-ku,Tokyo, Japan 113
Steric Effects of Silyl GroupsShwu-Chen TsayInstituteof Chemistry, Organosilicon and Synthesis Laboratory, Academia Sinica, Nankang, Taipei,Taiwan, Peoples’ Republic of China 11529 andNational TsingHua University, Department of Chemistry, Hsinchu, Taiwan, Peoples’ Republic of China30043
148
Silatranes and their Tricyclic AnalogsMikhail VoronkovSiberian Branch of the Russian Academy of Sciences, Irkutsk Institute of Chemistry, 1 Favorsky St, Irkutsk,Russia 664033
Chirality in Bioorganosilicon ChemistryStephan A. WagnerUniversitat Wurzburg, Institut fur Anorganische Chemie, Am Hubland, Wurzburg, Germany D-97074
ThermochemistryRobin WalshUniversity of Reading, Department of Chemistry, PO Box 224, Whiteknights, Reading, UK RG6 6AD
SilylenesRobert WestUniversity of Wisconsin at Madison, Department of Chemistry, Madison, WI 53706, USA
Organo-Silica Sol–Gel MaterialsAnna B. WojcikRutgers—The State University of New Jersey, Ceramics Department, Piscataway, NJ 08855-0909, USA
Recent Advances in the Hydrosilylation and Related ReactionsJiawang ZhuState University of New York at Stony Brook, Department of Chemistry, Stony Brook, NY 11794-3400, USA
Silicon–Carbon and Silicon–Nitrogen Multiply Bonded CompoundsWolfgang ZicheFachinstitut fur Anorganische und Allgemeine Chemie der Humboldt Universitat Berlin, Berlin, FRG D10115
The Chemistry of Organic Derivatives of Gold and Silver (1999)Edited by Saul Patai and Zvi Rappoport
Pyrolysis of Organic Derivatives of Silver and GoldR. Alan AitkenUniversity of St. Andrews, School of Chemistry, St. Andrews, Fife, UK KY16 9ST
General and Theoretical Aspects of Organic Gold CompoundsHarold BaschBar-Ilan University, Department of Chemistry, Ramat-Gan, Israel 52900
Synthesis and Uses of Organosilver CompoundsAngela BaylerTechnische Universitat Munchen, Lehrstuhl fur Anorganische und Analytische Chemie, Garching, GermanyD-85747
The Electrochemistry of Gold and Silver ComplexesAlice E. BruceUniversity of Maine, Department of Chemistry, Orono, ME 04469-5706, USA
149
The Electrochemistry of Gold and Silver ComplexesMitchell R. M. BruceUniversity of Maine, Department of Chemistry, Orono, ME 04469-5706, USA
Gold–Thiol Self-Assembled MonolayersVictor ChechikUniversity of Sheffield, Department of Chemistry, Sheffield, UKS3 7HF
Rearrangement of Gold and Silver ComplexesJohn P. Fackler Jr.Texas A&M University, Department of Chemistry, College Station, TX 77843-3012, USA
NMR and ESR Spectroscopy Applied to Gold and Silver CompoundsC Frank Shaw IIIUniversity of Wisconsin-Milwaukee, Department of Chemistry, P O Box 413, Milwaukee, WI 53201-0413,USA
Medicinal Chemistry of Gold CompoundsSimon P. FrickerAnorMED Inc., #100 20353-64 thAvenue, Langley, British Columbia, Canada V2Y 1N5
Analytical Aspects of Organogold and Organosilver CompoundsSarina GrinbergBen-Gurion University of the Negev, Institutes for Applied Research, Beer-Sheva, Israel
Synthesis and Uses of Organogold CompoundsAndreas GrohmannTechnische Universitat Munchen, Lehrstuhl fur Anorganische und Analytische Chemie, Garching, GermanyD-85747
The Organic Photochemistry of Silver and GoldWilliam M. HorspoolThe University of Dundee, Department of Chemistry, Dundee, Scotland DD1 4HN
General and Theoretical Aspects of Organic Gold CompoundsTova HozBar-Ilan University, Department of Chemistry, Ramat-Gan, Israel 52900
Syntheses and Uses of Isotopically Labelled Compounds of Silver and GoldMarianna KanskaUniversity of Warsaw, Department of Chemistry, Warsaw, Poland
Syntheses and Uses of Isotopically Labelled Compounds of Silver and GoldRyszard KanskiUniversity of Warsaw, Department of Chemistry, Warsaw, Poland
Acidity, Basicity and H BondsThomas M. KlapotkeUniversity of Munich (LMU), Institute of Inorganic Chemistry, Meiserstrasse 1, D-80333 Munich,Germany
150
Thermochemistry of the Organometallic Compounds of Silver and GoldJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
The Electrochemistry of Gold and Silver ComplexesAhmed A. MohamedUniversity of Maine, Department of Chemistry, Orono, ME 04469-5706, USA
The Photoelectron Spectroscopy of Organic Derivatives of Gold and SilverIgor NovakNational University of Singapore, Department of Chemistry, Singapore, Singapore 119260
Synthesis and Uses of Organogold CompoundsM. Elena OlmosTechnische Universitat Munchen, Lehrstuhl fur Anorganische und Analytische Chemie, Garching, GermanyD-85747
Mossbauer Spectroscopy with Gold CompoundsR. V. ParishUMIST, Department of Chemistry, PO Box 88, Manchester, UK M60 1QD
Synthesis and Uses of Organogold CompoundsAnnette SchierTechnische Universitat Munchen, Lehrstuhl fur Anorganische und Analytische Chemie, Garching, GermanyD-85747
Synthesis and Uses of Organogold CompoundsHubert SchmidbaurTechnische Universitat Munchen, Lehrstuhl fur Anorganische und Analytische Chemie, Garching, GermanyD-85747
Synthesis and Uses of Organosilver CompoundsHubert SchmidbaurTechnische Universitat Munchen, Lehrstuhl fur Anorganische und Analytische Chemie, Garching, GermanyD-85747
Thermochemistry of the Organometallic Compounds of Silver and GoldJose Martinho SimoesUniversidade de Lisboa, Departamento de Quımica e Bioquımica and CiTecMat, Faculdade de Ciencias,1700 Lisboa, Portugal
Thermochemistry of the Organometallic Compounds of Silver and GoldSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA
Gold–Thiol Self-Assembled MonolayersCharles J. M. StirlingUniversity of Sheffield, Department of Chemistry, Sheffield, UK S3 7HF
Rearrangement of Gold and Silver ComplexesSuning WangQueen’s University, Department of Chemistry, Kingston, Ontario, Canada K7L 3N6
151
Analytical Aspects of Organogold and Organosilver CompoundsJacob ZabickyBen-Gurion University of the Negev, Institutes for Applied Research, Beer-Sheva, Israel
Syntheses and Uses of Isotopically Labelled Compounds of Silver and GoldMieczysŁaw ZielinskiJagiellonian University, Isotope Laboratory, Faculty of Chemistry, Cracow, Poland
The Chemistry of Dienes and Polyenes (2000) (See Volume 1 in 1997)
Edited by Zvi Rappoport
Intermolecular Cyclization Reactions to form CarbocyclesPatrick H BeuskerUniversity of Nijmegen, Department of Organic Chemistry, NSR Center for Molecular Structure, Designand Synthesis, Toernooiveld, Nijmegen, ED, The Netherlands 6525
Cycloaddition to Give HeterocyclesGerhard V. BoydThe Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904
Electrophilic Additions to Dienes and PolyenesCinzia ChiappeUniversita di Pisa, Dipartimento di Chimica Bioorganica e Biofarmacia, Via Bonanno 33, Pisa, Italy56126
Synthetic Applications of Dienes and Polyenes, Excluding CycloadditionsKimberly A. ConlonState University of New York at Stony Brook, Department of Pharmacological Sciences, School ofMedicine, Stony Brook, NY 11794-8651, USA
Photopericyclic Reactions of Conjugated Dienes and TrienesBruce H. O. CookMcMaster University, Department of Chemistry, 1280 Main St. W., Hamilton, Ontario, CanadaL8S 4M1
Organometallic Complexes of Dienes and PolyenesWilliam A. DonaldsonMarquette University, Department of Chemistry, P. O. Box 1881, Milwaukee, WI 53201-1881, USA
Reduction of Dienes and PolyenesG. FarkasTechnical University of Budapest, Department of Chemical Technology, Budafoki ut 8, Budapest, HungaryH-1521
Reduction of Dienes and PolyenesK. FodorTechnical University of Budapest, Department of Chemical Technology, Budafoki ut 8, Budapest, HungaryH-1521
Reduction of Dienes and PolyenesA. FurchtTechnical University of Budapest, Department of Chemical Technology, Budafoki ut 8, Budapest, HungaryH-1521
152
Reduction of Dienes and PolyenesL. HegedusTechnical University of Budapest, Department of Chemical Technology, Budafoki ut 8, Budapest, HungaryH-1521
Photochemistry of Non-Conjugated DienesWilliam M. HorspoolThe University of Dundee, Department of Chemistry, Dundee, Scotland, UK DD1 4HN
Reduction of Dienes and PolyenesZs. P. KarancsiTechnical University of Budapest, Department of Chemical Technology, Budafoki ut 8, Budapest, HungaryH-1521
Rearrangements of Dienes and PolyenesAlla V. KoblikRostov State University, Institute of Physical and Organic Chemistry, Stachki str., 194/2, Rostov on Don,Russia 344104
Nucleophilic Additions to Dienes, Enynes and PolyenesNorbert KrauseUniversity of Dortmund, Organic Chemistry II, Dortmund, Germany D-44221
Mass Spectrometry and Gas-Phase Ion Chemistry of Dienes and PolyenesDietmar KuckUniversitat Bielefeld, Fakultat fur Chemie, Universitatsstraße 25, Bielefeld, Germany D-33615 andUniversitat-Gesamthochschule Paderborn, Germany and Fachbereich Chemie und Chemietechnik,Warburger Straße 100, Paderborn, Germany D-33098
Photopericyclic Reactions of Conjugated Dienes and TrienesWilliam J. LeighMcMaster University, Department of Chemistry, 1280 Main St. W., Hamilton, Ontario, Canada L8S 4M1
Rearrangements of Dienes and PolyenesSergei M. LukyanovRostov State University, Institute of Physical and Organic Chemistry, Stachki str., 194/2, Rostov on Don,Russia 344104
Mass Spectrometry and Gas-Phase Ion Chemistry of Dienes and PolyenesMichael MormannUniversitat-Gesamthochschule Paderborn, Fachbereich Chemie und Chemietechnik, Warburger Straße100, Paderborn, Germany D-33098
Electrophilic Additions to Dienes and PolyenesMarie-Francoise Ruassel’Universite Paris 7-Denis Diderot, Institut de Topologie et de Dynamique des Systemes de, associe auCNRS, UPRESA 7086, 1, rue Guy de la Brosse, Paris, France 75005
Intermolecular Cyclization Reactions to form CarbocyclesHans W ScheerenUniversity of Nijmegen, Department of Organic Chemistry, NSR Center for Molecular Structure, Designand Synthesis, Toernooiveld, Nijmegen, ED, The Netherlands 6525
153
Catalysis of Diels–Alder Reactions in Water and in Hydrogen-Bonding EnvironmentsPeter R. SchreinerGeorg-August Universitat Gottingen, Institute fur Organische Chemie, Tammannstr. 2, Gottingen,Germany D-37077
NMR Spectroscopy of Dienes and PolyenesToshio TakayamaKanagawa University, Department of Applied Chemistry, Faculty of Engineering, 3-27-1 Rokkakubashi,Yokohama, Japan 221-8686
NMR Spectroscopy of Dienes and PolyenesYoshito TakeuchiKanagawa University, Department of Chemistry, Faculty of Science, 2946 Tsuchiya, Hiratsuka, Japan259-1293
Reduction of Dienes and PolyenesA. TunglerTechnical University of Budapest, Department of Chemical Technology, Budafoki ut 8, Budapest, HungaryH-1521
Synthetic Applications of Dienes and Polyenes, Excluding CycloadditionsNanette Wachter-JurcsakHofstra University, Department of Chemistry, Biochemistry and Natural Science, Hempstead, NY11549-1090, USA
Catalysis of Diels–Alder Reactions in Water and in Hydrogen-Bonding EnvironmentsAlexander WittkoppGeorg-August Universitat Gottingen, Institute fur Organische Chemie, Tammannstr. 2, Gottingen,Germany D-37077
Nucleophilic Additions to Dienes, Enynes and PolyenesClaudia ZelderUniversity of Dortmund, Organic Chemistry II, Dortmund, Germany D-44221
The Chemistry of Organic Silicon Compounds Volume 3 (2001) (See Volume 1 in 1989,Volume 2 in 1998)
Edited by Zvi Rappoport and Yitzhak Apeloig
Theoretical Aspects of Compounds Containing Si, Ge, Sn and PbYitzhak ApeloigTechnion-Israel Institute of Technology, Department of Chemistry, and the Lise Meitner Minerva, 32000,Haifa, Israel
(Helium I)-Photoelectron Spectra of Silicon Compounds: History and Achievements Concerningtheir Molecular StatesH. BockJohann Wolfgang Goethe University, Institute of Inorganic Chemistry, Marie-Curie Street 11, Frankfurtam Main, Germany D-60439
154
Nanostructured Hybrid Organic–Inorganic Solids from Molecules to MaterialsBruno BouryUniversite de Montpellier II, Laboratoire de Chimie Moleculaire et Organisation du Solide UMR 5637,CC007, Place E. Bataillon, Montpellier cedex, France 34095
Silyl RadicalsC. ChatgilialogluConsiglio Nazionale delle Ricerche, I.Co.C.E.A., Via P. Gobetti 101, Bologna, Italy 40129
Chemistry on Silicon SurfacesCheol Ho ChoiIowa State University, Department of Chemistry, Ames, IA 50011, USA
Nanostructured Hybrid Organic–Inorganic Solids from Molecules to MaterialsRobert J. P. CorriuUniversite de Montpellier II, Laboratoire de Chimie Moleculaire et Organisation du Solide UMR 5637,CC007, Place E. Bataillon, Montpellier cedex, France 34095
Ion–Molecule Reactions of Silicon CationsSimonetta FornariniUniversita di Roma “La Sapienza”, Dipartimento di Studi di Chimica e Tecnologia delle SostanzeBiologicamente Attive, P.le A. Moro 5, Roma, Italy I-00185
Chemistry on Silicon SurfacesMark S GordonIowa State University, Department of Chemistry, Ames, IA 50011, USA
Organosilicon Halides—Synthesis and PropertiesUwe HerzogInstituteof Inorganic Chemistry, Freiberg University of Mining and Technology, Leipziger Str. 29,Freiberg, Germany D-09596
Silyl MigrationsTakeaki IwamotoTohoku University, Graduate School of Science, Department of Chemistry, Aoba-ku, Sendai, Japan980-8578
Recent Developments in the Chemistry of Compounds with Silicon–Nitrogen BondsBettina JaschkeUniversity of Goettingen, Institute of Inorganic Chemistry, Tammannstr. 4, Goettingen, Germany D-37077
Theoretical Aspects of Compounds Containing Si, Ge, Sn and PbJurgen KappThe University of Erlangen-Nurnberg, Computer Chemistry Center of the Institute of Organic Chemistry,Henkestrasse 42, Erlangen, Germany 91054
Theoretical Aspects of Compounds Containing Si, Ge, Sn and PbMiriam KarniTechnion-Israel Institute of Technology, Department of Chemistry, and the Lise Meitner Minerva, 32000,Haifa, Israel
155
Silyl MigrationsMitsuo KiraTohoku University, Graduate School of Science, Department of Chemistry, Aoba-ku, Sendai, Japan980-8578
Recent Developments in the Chemistry of Compounds with Silicon–Nitrogen BondsUwe KlingebielUniversity of Goettingen, Institute of Inorganic Chemistry, Tammannstr. 4, Goettingen, Germany D-37077
Kinetic Studies of the Reactions of Si=C and Si=Si BondsWilliam J. LeighMcMaster University, Department of Chemistry, 1280 Main Street West, Hamilton, Ontario, Canada L8S4M1
PolysilanolsPaul D LickissImperial College of Science Technology and Medicine, Department of Chemistry, London, England SW72AY
Kinetic Studies of the Reactions of Si=C and Si=Si BondsTracy L. MorkinMcMaster University, Department of Chemistry, 1280 Main Street West, Hamilton, Ontario, CanadaL8S4M1
Biotechnology Reveals New Routes to Synthesis and Structural Control of Silica andPolysilsesquioxanesDaniel E. MorseUniversity of California, MarineBiotechnologyCenter and Department of Molecular, Cellular andDevelopmental Biology, Santa Barbara, CA 93106, USA
Recent Developments in the Chemistry of Compounds with Silicon–Nitrogen BondsPeter NeugebauerUniversity of Goettingen, Institute of Inorganic Chemistry, Tammannstr. 4, Goettingen, Germany D-37077
Kinetic Studies of the Reactions of Si=C and Si=Si BondsThomas R. OwensMcMaster University, Department of Chemistry, 1280 Main Street West, Hamilton, Ontario, CanadaL8S4M1
Silyl RadicalsC.H. SchiesserThe University of Melbourne, Victoria, School of Chemistry, Victoria, Australia 3010
Theoretical Aspects of Compounds Containing Si, Ge, Sn and PbPaul von R. SchleyerThe University of Erlangen-Nurnberg, Computer Chemistry Center of the Institute of Organic Chemistry,Henkestrasse 42, Erlangen, Germany 91054
29Si NMR Experiments in Solutions of Organosilicon CompoundsJan SchramlInstitute of Chemical Process Fundamentals, Academy of Sciences of the Czech Republic, Prague, CzechRepublic 165 02
156
(Helium I)-Photoelectron Spectra of Silicon Compounds: History and Achievements Concerningtheir Molecular StatesB. SoloukiJohann Wolfgang Goethe University, Institute of Inorganic Chemistry, Marie-Curie Street 11, Frankfurtam Main, Germany D-60439
Silicon-Based Dendrimers and Hyperbranched PolymersDavid Y SonSouthern Methodist University, Department of Chemistry, P.O. Box 750314, Dallas, TX, USA
Polysiloles and Related Silole-Containing PolymersKohei TamaoKyoto University, Institute for Chemical Research, Uji, Kyoto, Japan 611-0011
Synthesis of Multiply Bonded Phosphorus Compounds Using Silylphosphines and SilylphosphidesKozo ToyotaTohoku University, Department of Chemistry, Graduate School of Science, Aoba-ku, Sendai, Japan980-8578
Recent Advances in the Chemistry of Silicon–Silicon Multiple BondsManfred WeidenbruchUniversitat Oldenburg, Fachbereich Chemie, Oldenburg, Germany D-26111
Polysilanes: Conformations, Chromotropism and ConductivityRobert WestUniversity of Wisconsin, Organosilicon Research Center, Department of Chemistry, Madison, WI 53706,USA
Polysiloles and Related Silole-Containing PolymersShigehiro YamaguchiKyoto University, Institute for Chemical Research, Uji, Kyoto, Japan 611-0011
Synthesis of Multiply Bonded Phosphorus Compounds Using Silylphosphines and SilylphosphidesMasaaki YoshifujiTohoku University, Department of Chemistry, Graduate School of Science, Aoba-ku, Sendai, Japan980-8578
The Chemistry of Organic Germanium, Tin and Lead Compounds (2003)(See Volume 1 in 1995)
Edited by Zvi Rappoport
Genesis and Evolution in the Chemistry of Organogermanium, Organotin and OrganoleadCompoundsKlavdiya A. AbzaevaA. E. Favorsky Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 FavorskyStr, Irkutsk, Russia 664033
Hypervalent Compounds of Organic Germanium, Tin and Lead DerivativesYuri I. BaukovRussian State Medical University, Department of General and Bioorganic Chemistry, 1 Ostrovityanov St,Moscow, Russia 117997
157
Spectroscopic Studies and Quantum-Chemical Calculations of Short-Lived Germylenes, Stannylenesand PlumbylenesSergey E. BoganovN. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prospect, 47,Moscow, Russian Federation 119991
Synthetic Uses of R3MH (M=Ge, Sn, Pb)Michael W. CarlandThe University of Melbourne, School of Chemistry, Melbourne, Victoria, Australia 3010
Alkaline and Alkaline Earth Metal-14 Compounds: Preparation, Spectroscopy, Structure andReactivityAnnie CastelUniversite Paul Sabatier, Laboratoire d’Heterochimie Fondamentale et Appliquee, UMR 5069 du CNRS,Toulouse cedex, France 31062
Structural Effects on Germanium, Tin and Lead CompoundsMarvin ChartonSchool of Liberal Arts and Sciences, Pratt Institute, Chemistry Department, Brooklyn, NY 11205, USA
Similarities and Differences of Organic Compounds of Germanium, Tin and LeadAlexey N. EgorochkinG. A. Razuvaev Institute of Metallorganic Chemistry of the Russian Academy of Sciences, 49 Tropinin Str.,Nizhny Novgorod, Russia 603950
Spectroscopic Studies and Quantum-Chemical Calculations of Short-Lived Germylenes, Stannylenesand PlumbylenesMikhail P. EgorovN. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prospect, 47,Moscow, Russian Federation 119991
Spectroscopic Studies and Quantum-Chemical Calculations of Short-Lived Germylenes, Stannylenesand PlumbylenesValery I. FaustovN. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prospect, 47,Moscow, Russian Federation 119991
Synthetic Applications of Organic Germanium, Tin and Lead Compounds (Excluding R3MH)Eric FouquetUniversite Bordeaux I, Laboratoire de Chimie Organique et Organometallique, 351, Cours de laLiberation, Talence Cedex, France 33405
Theoretical Studies of Organic Germanium, Tin and Lead CompoundsGernot FrenkingPhilipps-Universitat Marburg, Fachbereich Chemie, Hans-Meerwein-Strasse, Marburg, Germany D-35032
Theoretical Studies of Organic Germanium, Tin and Lead CompoundsInga GanzerPhilipps-Universitat Marburg, Fachbereich Chemie, Hans-Meerwein-Strasse, Marburg, Germany D-35032
Transition Metal Complexes of Germanium, Tin and LeadIonel HaiducUniversity of Texas at El Paso, Department of Chemistry, El Paso, TX 79968, USA
158
Theoretical Studies of Organic Germanium, Tin and Lead CompoundsMichael HartmannPhilipps-Universitat Marburg, Fachbereich Chemie, Hans-Meerwein-Strasse, Marburg, Germany D-35032
Biological Activity of Organogermanium CompoundsLuba IgnatovichLatvian Institute of Organic Synthesis, Aizkraukles 21, Riga, Latvia LV-1006
Organometallic Polymers of Germanium, Tin and LeadKlaus JurkschatLehrstuhl fur Anorganische Chemie II der Universitat Dortmund, Dortmund, Germany D-44221
Recent Advances in Acidity, Complexing, Basicity and H-Bonding of Organo Germanium, Tin andLead CompoundsThomas M. KlapotkeLudwig-Maximilians-University Munich, Department of Chemistry, Butenandtstr. 5–13 (Building D),Munich, Germany D-81377
Recent Advances in Structural Chemistry of Organic Germanium, Tin and Lead CompoundsKarl W KlinkhammerUniversity of Stuttgart, Institute for Inorganic Chemistry, Pfaffenwaldring 55, Stuttgart, Germany D-70569
Trichlorogermane, a New Superacid in Organic ChemistryStanislav KolesnikovN. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prospect,Moscow, Russian Federation 119991
Radical Reaction Mechanisms of and at Organic Germanium, Tin and LeadAlexander I. KruppaInstitute of Chemical Kinetics and Combustion, Novosibirsk-90, Russia 630090
Cage Compounds of Heavier Group 14 Elements
Unsaturated Three-Membered Rings of Heavier Group 14 ElementsVladimirYa. LeeUniversity of Tsukuba, Department of Chemistry, Tsukuba, Ibaraki, Japan 305-8571
Radical Reaction Mechanisms of and at Organic Germanium, Tin and LeadTatyana V. LeshinaInstitute of Chemical Kinetics and Combustion, Novosibirsk-90, Russia 630090
The Photochemistry of Organometallic Compounds of Germanium, Tin and LeadConor LongSchoolof Chemical Sciences, DublinCity University, Dublin 9, Ireland
Biological Activity of Organogermanium Compounds
Biological Activity of Organotin and Organolead CompoundsEdmunds LukevicsLatvian Institute of Organic Synthesis, Aizkraukles 21, Riga, Latvia LV-1006
159
Further Advances in Germanium, Tin and Lead NMRHeinrich Chr. MarsmannUniversitat Paderborn, Fachbereich Chemie, Anorganische Chemie, Warburger Straße 100, Paderborn,Germany D-30095
Organometallic Polymers of Germanium, Tin and LeadMichael MehringLehrstuhl fur Anorganische Chemie II der Universitat Dortmund, Dortmund, Germany D-44221
Free and Complexed R3M+ Cations (M=Ge, Sn, Pb)Josef MichlUniversity of Colorado, Department of Chemistry and Biochemistry, Boulder, CO 80309-0215, USA
Spectroscopic Studies and Quantum-Chemical Calculations of Short-Lived Germylenes, Stannylenesand Plumbylenes
Trichlorogermane, a New Superacid in Organic ChemistryOleg M. NefedovN. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prospect,Moscow, Russian Federation 119991
Multiply Bonded Germanium, Tin and Lead CompoundsRenji OkazakiJapan Women’s University, Department of Chemical and Biological Sciences, Faculty of Science, 2-8-1Mejirodai, Bunkyo-ku, Tokyo, Japan 112-8681
Transition Metal Complexes of Germanium, Tin and LeadKeith H. PannellUniversity of Texas at El Paso El Paso, Department of Chemistry, TX 79968, USA
The Photochemistry of Organometallic Compounds of Germanium, Tin and LeadMary T. PryceSchool of Chemical Sciences, DublinCity University, Dublin 9, Ireland
Biological Activity of Organotin and Organolead CompoundsOlga PudovaLatvian Institute of Organic Synthesis, Aizkraukles 21, Riga, Latvia LV-1006
Recent Advances in Acidity, Complexing, Basicity and H-Bonding of Organo Germanium, Tin andLead CompoundsClaudia M. RienackerLudwig-Maximilians-University Munich, Department of Chemistry, Butenandtstr. 5–13 (Building D),Munich, Germany D-81377
Gas-Phase Chemistry and Mass Spectrometry of Ge-, Sn- and Pb-Containing CompoundsJose M. RiverosUniversity of Sao Paulo, Institute of Chemistry, Caixa Postal 26077, Sao Paulo, Brazil CEP 05513-970
Alkaline and Alkaline Earth Metal-14 Compounds: Preparation, Spectroscopy, Structure andReactivityPierre RiviereUniversite Paul Sabatier, Laboratoire d’Heterochimie Fondamentale et Appliquee , UMR 5069 du CNRS,Toulouse cedex, France 31062
160
Alkaline and Alkaline Earth Metal-14 Compounds: Preparation, Spectroscopy, Structure andReactivityMonique Riviere-BaudetUniversite Paul Sabatier, Laboratoire d’Heterochimie Fondamentale et Appliquee , UMR 5069 du CNRS,Toulouse cedex, France 31062
Synthetic Uses of R3MH (M=Ge, Sn, Pb)Carl H. SchiesserThe University of Melbourne, School of Chemistry, Melbourne, Victoria, Australia 3010
Cage Compounds of Heavier Group 14 Elements
Unsaturated Three-Membered Rings of Heavier Group 14 ElementsAkira SekiguchiUniversity of Tsukuba, Department of Chemistry, Tsukuba, Ibaraki, Japan 305-8571
Transition Metal Complexes of Germanium, Tin and LeadHemant K. SharmaUniversity of Texas at El Paso, Department of Chemistry, El Paso, TX 79968, USA
Gas-Phase Chemistry and Mass Spectrometry of Ge-, Sn- and Pb-Containing CompoundsKeiko TakashimaUniversity of Londrina, Department of Chemistry, Caixa Postal 6001, Londrina, PR, Brazil CEP86051-970
Hypervalent Compounds of Organic Germanium, Tin and Lead Derivatives
Trichlorogermane, a New Superacid in Organic ChemistryStanislav N. TanduraN. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prospect,Moscow, Russia 119991
Radical Reaction Mechanisms of and at Organic Germanium, Tin and LeadMarc B. TarabanInstituteof Chemical Kinetics and Combustion, Novosibirsk-90, Russia 630090
Multiply Bonded Germanium, Tin and Lead CompoundsNorihiro TokitohKyoto University, Institute for Chemical Research, Gokasho, Uji, Kyoto, Japan 611-0011
Further Advances in Germanium, Tin and Lead NMRFrank UhligUniversitat Dortmund, Fachbereich Chemie, Anorganische Chemie II, Otto-Hahn-Str. 6, Dortmund,Germany D-44221
Radical Reaction Mechanisms of and at Organic Germanium, Tin and LeadOlga S. VolkovaInstitute of Chemical Kinetics and Combustion, Novosibirsk-90, Russia 630090
Genesis and Evolution in the Chemistry of Organogermanium, Organotin and OrganoleadCompounds
161
Similarities and Differences of Organic Compounds of Germanium, Tin and LeadMikhail G. VoronkovA. E. Favorsky Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 FavorskyStr., Irkutsk, Russia 664033
Free and Complexed R3M+ Cations (M=Ge, Sn, Pb)Ilya ZharovUniversity of Colorado, Department of Chemistry and Biochemistry, Boulder, CO, USA 80309-0215
The Chemistry of Phenols (2003)Edited by Zvi Rappoport
Phenols as AntioxidantsC. BarclayMount Allison University, Department of Chemistry, Sackville, New Brunswick, Canada E4L 1G8
Hydrogen-Bonded Complexes of PhenolsM. BerthelotUniversity of Nantes, Laboratoire de Spectrochimie, 2, rue de la Houssiniere BP 92208, Nantes Cedex 3,France F-44322
CalixarenesVolker BohmerJohannes Gutenberg-Universitat, Fachbereich Chemie und Pharmazie, Abteilung Lehramt Chemie,Duesbergweg 10–14, Mainz, Germany D-55099
Synthesis of PhenolsLuis CastedoUniversidad de Santiago de Compostela, Departamento de Quı mica Organica y Unidad Asociada alC.S.I.C., Facultad de Quı mica, Santiago de Compostela, Spain 15782
Polymers based on phenolsM. J. CaulfieldThe University of Melbourne, Polymer Science Group, Department of Chemical Engineering, Melbourne,Victoria, Australia 3010
Environmental Effects of Substituted PhenolsVictor GlezerMinistry of Health, National Public Health Laboratory, 69 Ben Zvi Rd., Tel Aviv, Israel
Synthesis of PhenolsConcepcion GonzalezUniversidad de Santiago de Compostela, Departamento de Quı mica Organica, Facultad de Ciencias,Lugo, Spain 27002
Hydrogen-Bonded Complexes of PhenolsJ. GratonUniversity of Nantes, Laboratoire de Spectrochimie, 2, rue de la Houssiniere BP 92208, Nantes Cedex 3,France F-44322
162
NMR and IR Spectroscopy of PhenolsPoul Erik HansenRoskilde University, Department of Life Sciences and Chemistry, Box 260, Roskilde, Denmark DK-4000
Photochemistry of PhenolsWilliam M. HorspoolThe University of Dundee, Department of Chemistry, Dundee, Scotland, UK DD1 4HN
The Structural Chemistry of PhenolsMenahem KaftoryTechnion—Israel Institute of Technology, Department of Chemistry, Haifa, Israel 32000
General and Theoretical Aspects of Phenolsgeneral and Theoretical Aspects of PhenolsEugene S. KryachkoUniversity of Leuven, Department of Chemistry, Belgium B-3001 andLimburgs Universitaire Centrum, Departement SBG, Diepenbeek, Belgium B-3590
Mass Spectrometry and Gas-Phase Ion Chemistry of PhenolsDietmar KuckFakultat fur Chemie, Universitat Bielefeld, Universitatsstraße 25, Bielefeld, Germany D-33615
Hydrogen-Bonded Complexes of PhenolsC. LaurenceUniversity of Nantes, Laboratoire de Spectrochimie, 2, rue de la Houssiniere BP 92208, Nantes Cedex 3,France F-44322
Thermochemistry of Phenols and Related ArenolsJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
Radiation Chemistry of Phenols
Transient Phenoxyl Radicals: Formation and Properties in Aqueous SolutionsP. NetaNational Institute of Standards and Technology, Gaithersburg, MD 20899, USA
General and Theoretical Aspects of Phenolsgeneral and Theoretical Aspects of PhenolsMinh Tho NguyenUniversity of Leuven, Department of Chemistry, Leuven, Belgium B-3001
UV-Visible Spectra and Photoacidity of Phenols, Naphthols and PyrenolsEhud PinesBen-Gurion University of the Negev, Chemistry Department, P.O.B. 653, Beer-Sheva, Israel 84105
Electrophilic Reactions of PhenolsV. Prakash ReddyUniversity of Missouri-Rolla, Department of Chemistry, Rolla, MO 65409, USA
Polymers based on phenolsG. G. QiaoThe University of Melbourne, Polymer Science Group, Department of Chemical Engineering, Melbourne,Victoria, Australia 3010
163
Phenols as AntioxidantsL. RossMount Allison University, Department of Chemistry, Sackville, New Brunswick, CanadaE4L 1G8
Thermochemistry of Phenols and Related ArenolsSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA
Polymers based on phenolsD. H. SolomonThe University of Melbourne, Polymer Science Group, Department of Chemical Engineering, Melbourne,Victoria, Australia 3010
NMR and IR Spectroscopy of PhenolsJens Spanget-LarsenRoskilde University, Department of Life Sciences and Chemistry, Box 260, Roskilde, Denmark DK-4000
Radiation Chemistry of Phenols
Transient Phenoxyl Radicals: Formation and Properties in Aqueous SolutionsS. SteenkenMax-Planck-Institut fur Strahlenchemie, D-45413, Mulheim, Germany
Electrophilic Reactions of PhenolsG. K. Surya PrakashUniversity of Southern California, Loker Hydrocarbon Research Institute and Department of Chemistry,Los Angeles, CA 90089-1661, USA
General and Theoretical Aspects of Phenolsgeneral and Theoretical Aspects of PhenolsLuc G. VanquickenborneUniversity of Leuven, Department of Chemistry, Leuven, Belgium B-3001
Phenols as AntioxidantsMelinda R. VinqvistMount Allison University, Department of Chemistry, Sackville, New Brunswick, CanadaE4L 1G8
Synthetic Uses of PhenolsMasahiko YamaguchiTohoku University, Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Aoba,Sendai, Japan 980-8578
Oxidation of PhenolsShosuke YamamuraKeio University, Department of Chemistry, Faculty of Science and Technology, Hiyoshi, Yokohama, Japan223-8522
Analytical Aspects of Phenolic CompoundsJacob ZabickyInstitutes for Applied Research, Ben-Gurion University of the Negev, P. O. Box 653, Beer-Sheva, Israel84105
164
The Chemistry of Organolithium Compounds, Volume 1 (2004) (See Volume 2 in 2006)
Edited by Zvi Rappoport and Ilan Marek
Lithium CarbenoidsManfred BraunUniversitat Dusseldorf, Institut fur Organische Chemie und Makromolekulare Chemie, Dusseldorf,Germany D-40225
Effects of Structural Variation on Organolithium CompoundsMarvin ChartonSchool of Liberal Arts and Sciences, Pratt Institute, Chemistry Department, Brooklyn, NY 11205, USA
Reactivity of Oxiranes with Organolithium ReagentsFabrice ChemlaUniversite Pierre et Marie Curie, Tour 44-45 2eme etage, Bte 183, Laboratoire de Chimie Organique, 4Place Jussieu, Paris Cedex 05, France F-75252
Asymmetric Deprotonation with Alkyllithium–(-)-SparteineGuido ChristophOrganisch-Chemisches Institut der Westfalischen Wilhelms-Universitat Munster, Corrensstr. 40, Munster,Germany D-48149
Directed Metallation of Aromatic CompoundsJonathan ClaydenUniversity of Manchester, Department of Chemistry, Oxford Road, Manchester, UK M13 9PL
α-Amino-Organolithium CompoundsIain ColdhamUniversity of Exeter, School of Chemistry, Stocker Road, Exeter, UK EX4 4QD
Gas Phase Chemistry of Organolithium CompoundsChagit DenekampTechnion–Israel Institute of Technology, Department of Chemistry, Technion City, Haifa, Israel 32000
α-Amino-Organolithium CompoundsRobert E. GawleyUniversity of Miami, Department of Chemistry, Coral Gables, FL 33124, USA
Theoretical Studies in Organolithium ChemistryG. GopakumarUniversity of Hyderabad, School of Chemistry, Gachibowli, Hyderabad, Andhra Pradesh, India 500 046
Solid State NMR Spectroscopy in Organolithium ChemistryHarald GuntherUniversity of Siegen, OCII, Fachbereich 8, Siegen, Germany D-57068
Asymmetric Deprotonation with Alkyllithium–(-)-SparteineDieter HoppeOrganisch-Chemisches Institut der Westfalischen Wilhelms-Universitat Munster, Corrensstr. 40, Munster,Germany D-48149
165
Theoretical Studies in Organolithium ChemistryEluvathingal D. JemmisUniversity of Hyderabad, School of Chemistry, Gachibowli, Hyderabad, Andhra Pradesh, India 500 046
Solid State NMR Spectroscopy in Organolithium ChemistryDan JohnelsUmeaUniversity, Department of Chemistry/Organic Chemistry, Umea, Sweden SE-901 87
Vibrational Spectroscopy of Organolithium CompoundsW. KieferUniversitat Wurzburg, Institut fur Physikalische Chemie, Am Hubland, Wurzburg, Germany D-97074
The Preparation of Organolithium Reagents and IntermediatesFred eric LerouxUniversite Louis Pasteur (ECPM), Laboratoire de stereochimie, 25 rue Becquerel, Strasbourg, FranceF-67087
Thermochemistry of Organolithium CompoundsJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
The Preparation of Organolithium Reagents and IntermediatesIlan MarekTechnion—Israel Institute of Technology, Department of Chemistry and Institute of Catalysis, Science andTechnology, Technion City, Haifa, Israel 32000
Vibrational Spectroscopy of Organolithium CompoundsI. PavelUniversitat Wurzburg, Institut fur Physikalische Chemie, Am Hubland, Wurzburg, Germany D-97074
Polylithium Organic Compounds: Syntheses and Selected Molecular StructuresDaniel SchildbachUniversitat Wurzburg, Institut fur Anorganische Chemie, Am Hubland, Wurzburg, Germany D-97074
The Preparation of Organolithium Reagents and IntermediatesManfred SchlosserSwiss Federal Institute of Technology, Institute of Molecular and Biological Chemistry, Lausanne,Switzerland CH-1015
Thermochemistry of Organolithium CompoundsSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA
Vibrational Spectroscopy of Organolithium CompoundsD. StalkeUniversitat Wurzburg, Institut fur Anorganische Chemie, Am Hubland, Wurzburg, Germany D-97074
Lead Structures in Lithium Organic ChemistryDietmar StalkeAm Hubland, Institut fur Anorganische Chemie der Bayerischen Julius-Maximilians Universitat Wurzburg,Wurzburg, Germany 97074
166
Lead Structures in Lithium Organic ChemistryThomas SteyAm Hubland, Institut fur Anorganische Chemie der Bayerischen Julius-Maximilians Universitat Wurzburg,Wurzburg, Germany 97074
Polylithium Organic Compounds: Syntheses and Selected Molecular StructuresCarsten StrohmannUniversitat Wurzburg, Institut fur Anorganische Chemie, Am Hubland, Wurzburg, Germany D-97074
Addition of Organolithium Reagents to Double BondsK. TomiokaKyoto University, Graduate School of Pharmaceutical Sciences, Sakyo-ku, Yoshida, Kyoto, Japan606-8501
Rearrangements of organolithium compoundsKatsuhiko TomookaTokyo Institute of Technology, Department of Applied Chemistry, Meguro-ku, Tokyo, Japan 152-8552
Reactivity of Oxiranes with Organolithium ReagentsEmmanuel VranckenUniversite Pierre et Marie Curie, Tour 44-45 2eme etage, Bte 183, Laboratoire de Chimie Organique, 4Place Jussieu, Paris Cedex 05, France F-75252
Addition of Organolithium Reagents to Double BondsK. YamadaKyoto University, Graduate School of Pharmaceutical Sciences, Sakyo-ku, Yoshida, Kyoto, Japan606-8501
Addition of Organolithium Reagents to Double BondsHiroshi YamatakaOsaka University, Institute of Scientific and Industrial Research, Osaka, Ibaraki, Japan 567-0047
Arene-Catalyzed LithiationMiguel YusUniversidad de Alicante, Departamento de Quımica Organica, Facultad de Ciencias, Apdo. 99, Alicante,Spain 03080
Analytical Aspects of Organolithium CompoundsJacob ZabickyBen-Gurion University of the Negev, Institutes for Applied Research, P. O. Box 653, Beer-Sheva, Israel84105
The Preparation of Organolithium Reagents and IntermediatesElinor ZoharTechnion—Israel Institute of Technology, Department of Chemistry and Institute of Catalysis, Science andTechnology, Technion City, Haifa, Israel 32000
167
The Chemistry of Cyclobutanes (2005)Edited by Zvi Rappoport and Joel F. Liebman
Acidity and Basicity of CyclobutanesJose Luis M. AbboudInstituto de Quımica Fısica ‘Rocasolano’, CSIC, C/Serrano, 119, Madrid, Spain E-28006
Acidity and Basicity of CyclobutanesIbon AlkortaInstituto de Quımica Medica, CSIC, C/Juan de la Cierva, 3, Madrid, Spain E-28006
Chemistry of Cubane and Other PrismanesA. Bashir-HashemiERC, Inc., at AFRL/PRS, 10 East Saturn Blvd., Edwards AFB, CA 93524, USA
Cation Radicals in the Synthesis and Reactions of CyclobutanesNathan L. BauldThe University of Texas at Austin, Department of Chemistry and Biochemistry, Austin, TX 78731, USA
Stereochemical Aspects—Conformation and ConfigurationUlf BergLund University, Organic Chemistry 1, Department of Chemistry, P. O. Box 124, Lund, Sweden S-221 00
Organometallic DerivativesHolger ButenschonUniversitat Hannover, Institut fur Organische Chemie, Schneiderberg 1B, Hannover, Germany D-30167
Cyclobutane Pyrimidine Dimers as UV-Induced DNA LesionsThomas CarellLMU Munchen, Department of Chemistry, Butenandtstraße 5–13 Haus F, Munchen, Germany D-81377
Bicyclo[2.1.0]pentanes and Bicyclo[2.2.0]hexanesBarry K. CarpenterCornell University, Department of Chemistry and Chemical Biology, Ithaca, NY 14853-1301, USA
The Application of Cyclobutane Derivatives in Organic SynthesisSiu-Hin ChanThe Chinese University of Hong Kong, Department of Chemistry, Institute of Chinese Medicine andCentral Laboratory of Institute of Molecular Technology for Drug Discovery and Synthesis, Shatin, NewTerritories, Hong Kong SAR, Peoples’ Republic of China
Structural Effects of the Cyclobutyl Group on Reactivity and PropertiesMarvin ChartonPratt Institute, Chemistry Department, School of Liberal Arts and Sciences, Brooklyn, NY 11205, USA
Fluorinated Cyclobutanes and Their DerivativesXudong ChenDartmouthCollege, Department of Chemistry, Hanover, NH 03755, USA
Acidity and Basicity of CyclobutanesJuan Z. DavalosInstituto de Quımica Fısica ‘Rocasolano’, CSIC, C/Serrano, 119, Madrid, Spain E-28006
168
NMR Spectroscopy of CyclobutanesJacques Fernandes DiasUniversidade Estadual do Rio de Janeiro, Departamento de Quımica e Ambiental, Faculdade deTecnologia, Estrada Resende-Riachuelo s/n◦, Resende, Brazil RJ 27523-000
Antiaromaticity and Aromaticity in Carbocyclic Four-Membered RingsM. Eckert-MaksicRudjer Boskovic Institute, Laboratory for Physical-Organic Chemistry, Division of Organic Chemistry andBiochemistry, Quantum Organic Chemistry Group, Zagreb, Croatia
Cyclobutane Pyrimidine Dimers as UV-Induced DNA LesionsMarcus G. FriedelLMU Munchen, Department of Chemistry, Butenandtstraße 5–13 Haus F, Munchen, Germany D-81377
The Application of Cyclobutane Derivatives in Organic SynthesisNan-Yan FuThe Chinese University of Hong Kong, Department of Chemistry, Institute of Chinese Medicine andCentral Laboratory of Institute of Molecular Technology for Drug Discovery and Synthesis, Shatin, NewTerritories, Hong Kong SAR, Peoples’ Republic of China
Cyclobutane Pyrimidine Dimers as UV-Induced DNA LesionsJohannes GierlichLMU Munchen, Department of Chemistry, Butenandtstraße 5–13 Haus F, Munchen, Germany D-81377
Chemistry of Cubane and Other PrismanesHiroyuki HiguchiToyama University, Department of Chemistry, Faculty of Science, 3190 Gofuku, Toyama, Toyama, Japan930-8555
Cubanes, Fenestranes, Ladderanes, Prismanes, Staffanes and Other OligocyclobutanoidsHenning HopfTechnical University of Braunschweig, Institute of Organic Chemistry, Hagenring 30, Braunschweig,Germany D-38106
Photochemistry of Cyclobutanes: Synthesis and ReactivityWilliam M. HorspoolThe University of Dundee, Department of Chemistry, Dundee, Scotland, UK DD1 4HN
Highly Unsaturated Cyclobutane DerivativesRichard P. JohnsonUniversity of New Hampshire, Department of Chemistry, Durham, NH 03824, USA
Mass Spectrometry and Gas-Phase Ion Chemistry of CyclobutanesDietmar KuckUniversitat Bielefeld, Fakultat fur Chemie, Universitatsstraße 25, Bielefeld, Germany D-33501
Synthesis of CyclobutanesE. Lee-RuffYork University, Department of Chemistry, Toronto, Ontario, Canada M3J 1P3
Fluorinated Cyclobutanes and Their DerivativesDavid M. LemalDartmouth College, Department of Chemistry, Hanover, NH 03755, USA
169
Cubanes, Fenestranes, Ladderanes, Prismanes, Staffanes and Other Oligocyclobutanoids
Thermochemistry of Cyclobutane and Its DerivativesJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
Antiaromaticity and Aromaticity in Carbocyclic Four-Membered RingsZ. B. MaksicRudjer Boskovic Institute, Laboratory for Physical-Organic Chemistry, Division of Organic Chemistry andBiochemistry, Quantum Organic Chemistry Group, Zagreb, Croatia
Solvent-Free Photosynthesis of Cyclobutanes: Photodimerization of Crystalline OlefinsArunkumar NatarajanTulane University, Department of Chemistry, New Orleans, LA 70118, USA
Cubanes, Fenestranes, Ladderanes, Prismanes, Staffanes and Other OligocyclobutanoidsH. Mark PerksUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
Acidity and Basicity of CyclobutanesEsther QuintanillaInstituto de Quımica Fısica ‘Rocasolano’, CSIC, C/Serrano, 119, Madrid, Spain E-28006
Solvent-Free Photosynthesis of Cyclobutanes: Photodimerization of Crystalline OlefinsV. RamamurthyTulane University, Department of Chemistry, New Orleans, LA 70118, USA
NMR Spectroscopy of CyclobutanesPeter Rudolf SeidlUniversidade Federal do Rio de Janeiro, Centro de Tecnologia Bloco E, Ilha do Fundao, Departamento deProcessos Organicos, Escola de Quımica, Rio de Janeiro, RJ, Brazil 21949-900
Cyclobutyl, Cyclobutyl-Substituted and Related CarbocationsHans-Ullrich SiehlAbteilung Organische Chemie I der Universitat Ulm, Albert Einstein Allee 11, Ulm, Germany D-89069
Thermochemistry of Cyclobutane and Its DerivativesSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA
CyclobutarenesAmnon StangerTechnion—Israel Institute of Technology, Department of Chemistry, The Lise Meitner-Minerva Center forComputational Quantum Chemistry, The Institute of Catalysis, Science and Technology, Haifa, Israel32000
Rearrangements of CyclobutanesJ. M. TankoVirginia Polytechnic Institute and State University, Department of Chemistry, Blacksburg, VA 24061, USA
170
Cyclobutane—Physical Properties and Theoretical StudiesKenneth B. WibergYale University, Department of Chemistry, New Haven, CT 06520-8107, USA
The Chemistry of Organolithium Compounds, Volume 2 (2006) (See Volume 1 in 2004)
Edited by Zvi Rappoport & Ilan Marek
Chiral Lithium Amides in Asymmetric SynthesisPer AhlbergGoteborg University, Department of Chemistry, Goteborg, Sweden SE-41296
Chiral Lithium Amides in Asymmetric SynthesisMohamed AmedjkouhGoteborg University, Department of Chemistry, Goteborg, Sweden SE-41296
The Lithium Metal Reduction of π-Conjugated Hydrocarbons and FullerenesIvan AprahamianThe Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904
Intramolecular Carbolithiation ReactionsFrancisco J. FananasUniversidad de Oviedo, Instituto Universitario de Quımica Organometalica “Enrique Moles”, UnidadAsociada al CSIC, C/Julian Claverıa, 8, Oviedo, Spain E-33006
Dynamics of the Reorganization Behavior of Organolithium CompoundsGideon FraenkelThe Ohio State University, Department of Chemistry, 100 W. 18th Avenue, Columbus, OH 43210, USA
Structure and Dynamics of Chiral Lithium AmidesJohan GrananderGoteborg University, Department of Chemistry, Kemivagen 10, Goteborg, Sweden SE-412 96
Structure and Dynamics of Chiral Lithium AmidesGoran HilmerssonGoteborg University, Department of Chemistry, Kemivagen 10, Goteborg, Sweden SE-412 96
Aspects of the Synthesis, Structure and Reactivity of Lithium EnolatesJacques MaddalunoUniversite de Rouen, Laboratoire des Fonctions Azotees & Oxygenees Complexes de l’IRCOF, UMR 6014CNRS, Mont St Aignan Cedex, France F-76821
Marek
The Chemistry of Acyllithium DerivativesCarmen NajeraUniversidad de Alicante, Departamento de Quımica Organica, Facultad de Ciencias, and Instituto deSıntesis Organica (ISO), Apdo. 99, Alicante, Spain E-03080
Chemistry of Ketone Dilithio DianionsHiroyuki NakahiraSumitomo Pharmaceuticals, Chemistry Research Laboratories, Research Division, Osaka, Japan 554-0022
171
Chiral Lithium Amides in Asymmetric SynthesisDaniel PettersenGoteborg University, Department of Chemistry, Goteborg, Sweden SE-41296
The Lithium Metal Reduction of π-Conjugated Hydrocarbons and FullerenesMordecai RabinovitzThe Hebrew University of Jerusalem, Department of Organic Chemistry, Jerusalem, Israel 91904
Chemistry of Ketone Dilithio DianionsIlhyong RyuOsaka Prefecture University, Department of Chemistry, Graduate School of Science, Sakai, Osaka, Japan599-8531
Intramolecular Carbolithiation ReactionsRoberto SanzUniversidad de Burgos, Departamento de Quımica, Facultad de Ciencias, Plaza Missael Banuelos s/n,Burgos, Spain E-09001
Organolithiums as Useful Synthetic Intermediates for Tandem ReactionsNorma Sbarbati NudelmanUniversidad de Buenos Aires, Depto. Quımica Organica, Facultad de Ciencias Exactas y Naturales, Pab.II, P 3 Ciudad Universitaria (1428), Buenos Aires, Argentina
Aspects of the Synthesis, Structure and Reactivity of Lithium EnolatesJean-Yves ValnotUniversite de Rouen, Laboratoire des Fonctions Azotees & Oxygenees Complexes de l’IRCOF, UMR 6014CNRS, Mont St Aignan Cedex, France F-76821
Organolithiums as Useful Synthetic Intermediates for Tandem ReactionsAlvaro J. VazquezUniversidad de Buenos Aires, Depto. Quımica Organica, Facultad de Ciencias Exactas y Naturales, Pab.II, P 3 Ciudad Universitaria (1428), Buenos Aires, Argentina
Organolithiums as Useful Synthetic Intermediates for Tandem ReactionsRaquel G. de WaisbaumUniversidad de Buenos Aires, Depto. Quımica Organica, Facultad de Ciencias Exactas y Naturales, Pab.II, P 3 Ciudad Universitaria (1428), Buenos Aires, Argentina
The Chemistry of Acyllithium DerivativesMiguel YusUniversidad de Alicante, Departamento de Quımica Organica, Facultad de Ciencias, and Instituto deSıntesis Organica (ISO), Apdo. 99, Alicante, Spain E-03080
The Chemistry of Peroxides, Volume 2 (2006) (See Volume 1 in 1983)
Edited by Zvi Rappoport
Contemporary Dioxirane Chemistry: Epoxidations, Heteroatom Oxidations and CH Insertions
Contemporary Trends in Dioxetane ChemistryWaldemar AdamUniversity of Wurzburg, Institute of Organic Chemistry, am Hubland, Wurzburg, Germany D-97094andUniversity of Puerto Rico, Department of Chemistry, Rio Piedras, Puerto Rico 00931, USA
172
Silicon and Germanium PeroxidesWataru AndoUniversity of Tsukuba, Department of Chemistry, Tennodai, Tsukuba, Ibaraki, Japan 305-8577
Chemiluminescence of Organic PeroxidesWilhelm J. BaaderUniversidade de Sao Paulo-Av. Prof. Lineu Prestes, Instituto de Quımica, 748 Bl., 12 S CEP, SaoPaulo—SP, Brazil 05508-900
General and Theoretical Aspects of the Peroxide GroupRobert D. BachUniversity of Delaware, Department of Chemistry and Biochemistry, Newark, DE 19716, USA
Synthesis of Cyclic PeroxidesMario D. BachiThe Weizmann Institute of Science, Department of Organic Chemistry, Rehovot, Israel 76100
Chemiluminescence of Organic PeroxidesErick L. BastosUniversidade de Sao Paulo-Av. Prof. Lineu Prestes, Instituto de Quımica, 748 Bl., 12 S CEP, SaoPaulo—SP, Brazil 05508-900
Synthetic Uses of PeroxidesAlbrecht BerkesselUniversity of Cologne, Department of Organic Chemistry, Greinstr. 4, Koln, Germany D-50939
Transition Metal Peroxides. Synthesis and Role in Oxidation ReactionsOlga BortoliniUniversita della Calabria, Dipartimento di Chimica, Via Bucci, cubo 12C, Rende (CS), Italy I-87036
Peroxides in Biological SystemsJean CadetLCIB-UMR-E n◦3 CEA-UJF, Laboratoire ‘Lesions des Acides Nucleiques’, Departement de RechercheFondamentale sur la Matiere Condensee , Grenoble Cedex 9, CEA/Grenoble, France F-38054
17O NMR Spectroscopy of Organic Compounds Containing the −O−O− groupGiovanni CerioniUniversita di Cagliari, Dipartimento Farmaco Chimico Tecnologico, Via Ospedale 72, Cagliari, ItalyI-09124
Biomimetic Fe(II) Chemistry and Synthetic Studies on Antimalarial and Antitumour EndoperoxidesJames ChadwickUniversity of Liverpool, Department of Chemistry, The Robert Robinson Laboratories, Liverpool, UKL697ZD
Transition Metal Peroxides. Synthesis and Role in Oxidation ReactionsValeria ConteUniversita di Roma “Tor Vergata”, Dipartimento di Scienze e Tecnologie Chimiche, via della RicercaScientifica, Roma, Italy I-00133
Peroxides in Biological SystemsPaolo Di MascioUniversidade de Sao Paulo, Ar. Prof. Lineu Prestes, Departamento de Bioquımica, Instituto de Quımica,748 CP 26077, Sao Paulo, SP, Brazil CEP 05513-970
173
The Structural Chemistry of Acyclic Organic PeroxidesJens HartungTechnische Universitat Kaiserslautern, Fachbereich Chemie, Organische Chemie,Erwin-Schrodinger-Straße , Kaiserslautern, Germany D-67663
Sulfur and Phosphorus PeroxidesVidyadhar JadhavKorea Advanced Institute of Science and Technology, Center for Molecular Design and Synthesis,Department of Chemistry, Taejon, Korea 305-701
Polar Effects in Decomposition of Peroxidic Compounds and Related ReactionsSung Soo KimInha University, Department of Chemistry, Incheon, South Korea 402-751
Sulfur and Phosphorus PeroxidesYong Hae KimKorea Advanced Institute of Science and Technology, Center for Molecular Design and Synthesis,Department of Chemistry, Taejon, Korea 305-701
Synthesis of Cyclic PeroxidesEdward E. KorshinThe Weizmann Institute of Science, Department of Organic Chemistry, Rehovot, Israel 76100
Thermochemistry of PeroxidesJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
17O NMR Spectroscopy of Organic Compounds Containing the −O−O− groupFrancesca MocciUniversita di Cagliari, Cittadella Universitaria di Monserrato, Dipartimento di Scienze Chimiche, SS 554Bivio per Sestu, Monserrato, (CA), Italy I-09024
Biomimetic Fe(II) Chemistry and Synthetic Studies on Antimalarial and Antitumour EndoperoxidesPaul M. O’NeillUniversity of Liverpool, Department of Chemistry, The Robert Robinson Laboratories, Liverpool, UK L697ZD
Selective Formation of Allylic Hydroperoxides via Singlet Oxygen ene ReactionMichael OrfanopoulosUniversity of Crete, Department of Chemistry, Iraklion, Greece G-71409
Sulfur and Phosphorus PeroxidesMinYoungParkKorea Advanced Institute of Science and Technology, Center for Molecular Design and Synthesis,Department of Chemistry, Taejon, Korea 305-701
Biomimetic Fe(II) Chemistry and Synthetic Studies on Antimalarial and Antitumour EndoperoxidesSarah L. RaweUniversity of Liverpool, Department of Chemistry, The Robert Robinson Laboratories, Liverpool, UKL697ZD
174
Thermochemistry of PeroxidesSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA
Chemiluminescence of Organic PeroxidesC. V. StevaniUniversidade de Sao Paulo-Av. Prof. Lineu Prestes, Instituto de Quımica, 748 Bl., 12 S CEP, SaoPaulo—SP, Brazil 05508-900
Selective Formation of Allylic Hydroperoxides via Singlet Oxygen ene ReactionManolis StratakisUniversity of Crete, Department of Chemistry, Iraklion, Greece G-71409
The Structural Chemistry of Acyclic Organic PeroxidesIngrid SvobodaTechnische Universitat Darmstadt, Fachgebiet Strukturforschung, FB 11, Material-und Geowissenschaften,Petersenstr. 23, Darmstadt, Germany D-64287
Contemporary Trends in Dioxetane ChemistryAlexei V. TrofimovRussian Academy of Sciences, Institute of Biochemical Physics, ul. Kosygina 4, Moscow, RussianFederation 119991 andUniversity of Wurzburg, Institute of Organic Chemistry, am Hubland, Wurzburg, Germany D-97094
Synthetic Uses of PeroxidesNadine VoglUniversity of Cologne, Department of Organic Chemistry, Greinstr. 4 Germany D-50939 Koln
Selective Formation of Allylic Hydroperoxides via Singlet Oxygen ene ReactionGeorgios C. VougioukalakisUniversity of Crete, Department of Chemistry, Iraklion, Greece G-71409
Analytical and Safety Aspects of Organic Peroxides and Related Functional GroupsJacob ZabickyBen-Gurion University of the Negev, Institutes for Applied Research, Department of ChemicalEngineering, Beer-Sheva, Israel 84105
Contemporary Dioxirane Chemistry: Epoxidations, Heteroatom Oxidations and CH InsertionsCong-Gui ZhaoUniversity of Texas at San Antonio, Department of Chemistry, San Antonio, TX 78249, USA
The Chemistry of Anilines (2007)Edited by Zvi Rappoport
Mass Spectrometry and Gas-Phase Chemistry of AnilinesDaniella Vasconcellos AugustiOctavio Magalhaes Institute, Ezequiel Diaz Foundation—FUNED, Belo Horizonte, MG, Brazil 30510-010
Mass Spectrometry and Gas-Phase Chemistry of AnilinesRodinei AugustiFederal University of Minas Gerais—UFMG, Department of Chemistry, Belo Horizonte, MG, Brazil31270-901
175
Synthesis of AnilinesFabiola Barrios-LanderosYale University, Department of Chemistry, P.O. Box 208107, New Haven, CT 06520 8107, USA
Mass Spectrometry and Gas-Phase Chemistry of AnilinesMarcos N. EberlinState University of Campinas, ThoMSon Mass Spectrometry Laboratory, Institute of Chemistry, Campinas,SP, Brazil 13084 971
Hydrogen Bonds of AnilinesLuciano ForlaniUniversity of Bologna, Dipartimento di Chimica Organica ‘A. Mangini’, Viale Risorgimento 4, Bologna,Italy 40136
NMR Spectra of AnilinesRyszard GawineckiFaculty of Chemical Technology and Engineering, University of Technology and Life Sciences,Seminaryjna 3, Bydgoszcz, PL, Poland 85 326
Synthesis of AnilinesJohn F. HartwigYale University, Department of Chemistry, P.O. Box 208107, New Haven, CT 06520 8107, USA
Electrochemistry of AnilinesJan S. JaworskiWarsaw University, Faculty of Chemistry, Warszawa, Poland 02-093
Electrochemistry of AnilinesMarek K. KalinowskiWarsaw University, Faculty of Chemistry, Warszawa, Poland 02-093
Rearrangements of Anilines and Their DerivativesAlla V. KoblikChemBridge Corporation, Malaya Pirogovskaya str., 1, Moscow, Russia 119435
NMR Spectra of AnilinesErkki KolehmainenUniversity of Jyvaskyla, Department of Chemistry, P.O. Box 35, Finland FIN-40014
Anilines as nucleophilesIkchoon LeeInha University, Department of Chemistry, Inchon, Korea 402-751
Thermochemistry of AnilinesJoel F. LiebmanUniversity of Maryland Balimore County, Department of Chemistry and Biochemistry, 1000 Hilltop Circle,Baltimore, MD 21250, USA
Rearrangements of Anilines and Their DerivativesSergei M. LukyanovChemBridge Corporation, Malaya Pirogovskaya str., 1, Moscow, Russia 119435
176
Substituted Anilines as Solvatochromic ProbesYizhak MarcusThe Hebrew University of Jerusalem, Department of Inorganic and Analytical Chemistry, Jerusalem, Israel91904
General and Theoretical Aspects of AnilinesMinh Tho NguyenUniversity of Leuven, Department of Chemistry and Institute for Nanoscale Physics and Chemistry,Celestijnenlaan 200F, Leuven, Belgium B-3001
NMR Spectra of AnilinesBorys OsmiałowskiFaculty of Chemical Technology and Engineering, University of Technology and Life Sciences,Seminaryjna 3, Bydgoszcz, PL, Poland 85 326
Proton SpongesValery A. OzeryanskiiRostov State University, Department of Organic Chemistry, Zorge str., 7, Rostov-on-Don, RussianFederation 344090
Proton SpongesAlexander F. PozharskiiRostov State University, Department of Organic Chemistry, Zorge str., 7, Rostov-on-Don, RussianFederation 344090
Synthesis of AnilinesShashank ShekharYale University, Department of Chemistry, P.O. Box 208107, New Haven, CT 06520 8107, USA
Synthesis of AnilinesQilong ShenYale University, Department of Chemistry, P.O. Box 208107, New Haven, CT 06520 8107, USA
Thermochemistry of AnilinesSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA
Anilines as nucleophilesDae Dong SungDong-A University, Department of Chemistry, Busan, Korea 604-714
Anilines: Historical Background
Manufacture and Uses of the Anilines: A Vast Array of Processes and Products
Toxicological and Environmental Aspects of AnilinesAnthony S. TravisThe Hebrew University of Jerusalem, Sidney M. Edelstein Center for the History and Philosophy ofScience, Technology and Medicine, Edmond J. Safra Campus, Givat Ram, Jerusalem, Israel 91904
Structural Chemistry of AnilinesGraz&c.uml;yna Maria WojcikWrocław University of Technology, Institute of Physical & Theoretical Chemistry, Wyb. Wyspianskiego 27,Wrocław, Poland 50-370
177
The Spectroscopy, Photophysics and Photochemistry of AnilinesJye-Shane YangNationalTaiwan University, Department of Chemistry, Taipei, Taiwan (ROC) 10617
Analytical Aspects of Aromatic AminesJacob ZabickyBen-Gurion University of the Negev, Department of Chemical Engineering, P.O. Box 653, Beer-Sheva,Israel 84105
The Chemistry of Organozinc Compounds (2007)Edited by Zvi Rappoport and Ilan Marek
Rearrangements of Organozinc CompoundsVarinder K. AggarwalUniversity of Bristol, School of Chemistry, Cantock’s Close, Bristol, United Kingdom BS8 1TS
Structural Organozinc ChemistryJaap BoersmaUtrecht University, Debye Institute, Organic Chemistry and Catalysis, Padualaan 8, Utrecht, CH, TheNetherlands 3584
Electrochemical Generation and Reaction of Zinc ReagentsOlivier BuriezUniversite Paris XII, C.N.R.S. UMR 7582, Laboratoire d’Electrochimie Catalyse et Synthese Organique,2–8 rue H. Dunant, Thiais, France F-94320
Fluorinated Organozinc ReagentsDonald J. BurtonUniversity of Iowa, Department of Chemistry, Iowa City, IA 52242, USA
Cyclopropanation Mediated by Zinc OrganometallicsAndre B. CharetteUniversite de Montreal, Department of Chemistry, P.O. Box 6128, Station Downtown, Montreal, Quebec,Canada H3C 3J7
The Reaction Mechanisms of Zinc EnzymesTimothy ClarkUniversity of Erlangen-Nurnberg, ComputerChemistryCenter, Nagelsbachstr. 25, Erlangen, GermanyD-91052
67Zn NMR, a Tool for Coordination Chemistry ProblemsAthanassios G. CoutsolelosUniversity of Crete, Chemistry Department, Laboratory of Bioinorganic Chemistry, PO Box 2208,Heraklion, Crete, Greece GR-71003
Fluorinated Organozinc ReagentsCharles R. DavisSigma-Aldrich, 6000 N. Teutonia Avenue, Milwaukee, WI 53209, USA
The Reaction Mechanisms of Zinc EnzymesRudi van EldikUniversity of Erlangen-Nurnberg, Institute for Inorganic Chemistry, Egerlandstr. 1, Erlangen, GermanyD-91058
178
Functionalized Organozinc CompoundsLiu-Zhu GongLudwig-Maximilians-Universitat Munchen, Department of Chemistry, Butenandtstr. 5–13, Munchen,Germany D-81377
Electrochemical Generation and Reaction of Zinc ReagentsCorinne GosminiUniversite Paris XII, C.N.R.S. UMR 7582, Laboratoire d’Electrochimie Catalyse et Synthese Organique,2–8 rue H. Dunant, Thiais, France F-94320
Dynamic Behavior of Organozinc CompoundsAlbert GuijarroUniversidad de Alicante, Departamento de Quımica Organica, Instituto de Sıntesis Organica (ISO), Ap.99, Alicante, Spain E-03080
The Chemistry of Organozincate CompoundsToshiro HaradaKyoto Institute of Technology, Department of Chemistry and Materials Technology, Matsugasaki,Sakyo-ku, Kyoto, Japan 606–8585
Palladium- or Nickel-Catalyzed Cross-Coupling Reactions with Organozincs and RelatedOrganometalsQian HuPurdue University, Herbert C. Brown Laboratories of Chemistry, 560 Oval Drive, West Lafayette, IN47907-2084, USA
Palladium- or Nickel-Catalyzed Cross-Coupling Reactions with Organozincs and RelatedOrganometalsZhihong HuangPurdue University, Herbert C. Brown Laboratories of Chemistry, 560 Oval Drive, West Lafayette, IN47907-2084, USA
Structural Organozinc ChemistryJohann T. B. H. JastrzebskiUtrecht University, Debye Institute, Organic Chemistry and Catalysis, Padualaan 8, Utrecht, CH, TheNetherlands 3584
Enantioselective Addition of Organozinc CompoundsTsuneomi KawasakiTokyo University of Science, Department of Applied Chemistry, Faculty of Science, Kagurazaka,Shinjuku-ku, Tokyo, Japan 162–8601
Functionalized Organozinc CompoundsFlorian F. KneiselLudwig-Maximilians-Universitat Munchen, Department of Chemistry, Butenandtstr. 5–13, Munchen,Germany D-81377
Functionalized Organozinc CompoundsPaul KnochelLudwig-Maximilians-Universitat Munchen, Department of Chemistry, Butenandtstr. 5–13, Munchen,Germany D-81377
179
Structural Organozinc ChemistryGerard van KotenUtrecht University, Debye Institute, Organic Chemistry and Catalysis, Padualaan 8, Utrecht, CH, TheNetherlands 3584
Functionalized Organozinc CompoundsHelena LeuserLudwig-Maximilians-Universitat Munchen, Department of Chemistry, Butenandtstr. 5–13, Munchen,Germany D-81377
Thermochemistry of Organozinc CompoundsJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore,, USA MD 21250, USA
The Chemistry of Zinc EnolatesMarco LombardoUniversity of Bologna, Department of Chemistry “G. Ciamician”, via Selmi 2, Bologna, Italy I-40126
Carbozincation of Alkenes and AlkynesEdwige LorthioisNovartis Pharma AG, Novartis Institutes for Biomedical Research, Protease Platform WKL-122-3-27,Klybeckstrasse 144, Basel, Switzerland CH-4002
Synthesis and Reactions of Allenylzinc ReagentsJames A. MarshallUniversity of Virginia, Department of Chemistry, PO Box 400319, Charlottesville, VA 22904, USA
1,1-Bismetallated SpeciesSeijiro MatsubaraKyoto University, Department of Material Chemistry, Graduate School of Engineering, Kyoudai-katsura,Nishikyo, Kyoto, Japan 606–8501
Carbozincation of Alkenes and AlkynesChristophe Meyerassocie au CNRS, ESPCI, Laboratoire de Chimie Organique, 10 rue Vauquelin, Paris Cedex 05, FranceF-75231
Palladium- or Nickel-Catalyzed Cross-Coupling Reactions with Organozincs and RelatedOrganometalsEi-Ichi NegishiPurdue University, Herbert C. Brown Laboratories of Chemistry, 560 Oval Drive, West Lafayette, IN47907-2084, USA
Mass Spectrometry of Organozinc CompoundsSergiu P. PaliiUniversity of Florida, Department of Chemistry, P.O. Box 117200, Gainesville, FL 32611-7200, USA
Electrochemical Generation and Reaction of Zinc ReagentsJacques PerichonUniversite Paris XII, C.N.R.S. UMR 7582, Laboratoire d’Electrochimie Catalyse et Synthese Organique,2–8 rue H. Dunant, Thiais, France F-94320
180
Functionalized Organozinc CompoundsSylvie PerroneLudwig-Maximilians-Universitat Munchen, Department of Chemistry, Butenandtstr. 5–13, Munchen,Germany D-81377
Enantioselective Addition of Organozinc CompoundsItaru SatoKwansei Gakuin University, Department of Chemistry, School of Science and Technology, Sanda, Hyogo,Japan 669–1337
The Reaction Mechanisms of Zinc EnzymesGudrun SchurerUniversity of Erlangen-Nurnberg, ComputerChemistryCenter, Nagelsbachstr. 25, Erlangen, GermanyD-91052
Photochemical Transformations Involving Zinc Porphyrins and PhthalocyaninesMathias O. SengeTrinity College Dublin, School of Chemistry, Dublin 2, Ireland
Photochemical Transformations Involving Zinc Porphyrins and PhthalocyaninesNatalia N. SergeevaTrinityCollegeDublin, School of Chemistry, Dublin 2, Ireland
Thermochemistry of Organozinc CompoundsSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA
Enantioselective Addition of Organozinc CompoundsKenso SoaiTokyo University of Science, Department of Applied Chemistry, Faculty of Science, Kagurazaka,Shinjuku-ku, Tokyo, Japan 162–8601
Rearrangements of Organozinc CompoundsKnut SommerUniversity of Bristol, School of Chemistry, Cantock’s Close, Bristol, United KingdomBS8 1TS
67Zn NMR, a Tool for Coordination Chemistry ProblemsGeorgios A. SpyrouliasUniversity of Patras, Department of Pharmacy, Panepistimioupoli—Rion, Patras, Greece GR-26504
The Chemistry of Zinc EnolatesClaudio TrombiniUniversity of Bologna, Department of Chemistry “G. Ciamician”, via Selmi 2, Bologna, Italy I-40126
Palladium- or Nickel-Catalyzed Cross-Coupling Reactions with Organozincs and RelatedOrganometalsGuangwei WangPurdue University, Herbert C. Brown Laboratories of Chemistry, 560 Oval Drive, West Lafayette, IN47907-2084, USA
181
Palladium- or Nickel-Catalyzed Cross-Coupling Reactions with Organozincs and RelatedOrganometalsNing YinPurdue University, Herbert C. Brown Laboratories of Chemistry, 560 Oval Drive, West Lafayette, IN47907-2084, USA
Mass Spectrometry of Organozinc CompoundsDmitri V. ZagorevskiiRensselaer Polytechnic Institute, Department of Chemistry and Chemical Biology, 209C CogswellLaboratories, 110 8th Str., Troy, NY 12180, USA
The Chemistry of Hydroxylamines, Oximes and Hydroxamic Acids, Volume 1 (2008)(See Volume 2 in 2010)
Edited by Zvi Rappoport and Joel F. Liebman
Synthesis of Heterocycles from OximesEdgars AbeleLatvian Institute of Organic Synthesis, Riga, Latvia LV1006
Hydroxylamines and Oximes: Biological Properties and Potential Uses as Therapeutic AgentsYacov AshaniThe Weizmann Institute of Science, Department of Neurobiology, Rehovot, Israel 76100
Natural and Biomimetic Hydroxamic Acid Based SiderophoresYaniv BardaWeizmann Institute of Science, Department of Organic Chemistry, P.O. Box 26, Rehovot, Israel 76100
Nitrosomethanides and their Acids: Synthesis, Structure and BondingHarald BrandLMU Munich, Butenandt-Str. 5–13, Munchen, Germany 81377
Hydroxylamine, Oximate and Hydroxamate as α-Nucleophiles in DephosphorylationErwin BuncelQueen’s University, Department of Chemistry, Kingston, Ontario, Canada K7L 3N6
Structural Effects on Reactivity and Properties of Oximes and Hydroxamic AcidsMarvin ChartonPratt Institute, Chemistry Department, School of Liberal Arts and Sciences, Brooklyn, NY 11205, USA
Electrophilic C-Amination with O-Substituted Hydroxylamines, Oximes and O-Substituted OximesEnder ErdikAnkara University Science Faculty, Department of Chemistry, Besevler, Ankara, Turkey 06100Edited by Zvi Rappoport and Joel F. Liebman
Natural and Biomimetic Hydroxamic Acid Based SiderophoresClifford E. FelderWeizmann Institute of Science, Department of Organic Chemistry, P.O. Box 26, Rehovot, Israel 76100
NMR Spectra of Hydroxylamines, Oximes and Hydroxamic AcidsJacques Fernandes DiasUniversidade do Estado do Rio de Janeiro, Departamento de Quımica e Ambiental, Faculdade deTecnologia, Rodovia Presidente Dutra km 298—Polo Industrial, Resende, Brazil RJ 27537-000
182
Nitroxyl RadicalsCarlo GalliUniversita ‘La Sapienza’ and IMC-CNR Sezione Meccanismi di Reazione, Dipartimento di Chimica,Roma, Italy 00185
Synthesis of Oximes and Hydroxamic AcidsGiampaolo GiacomelliUniversita degli Studi di Sassari, Dipartimento di Chimica, via Vienna 2, Italy 07100-Sassari
N-Heteroatom-Substituted Hydroxamic EstersStephen A. GloverUniversity of New England, Division of ChemistrySchool of Science and Technology, Armidale, NSW,Australia 2351
The Organic Thermochemistry of Hydroxylamines, Oximes, Hydroxamic Acids and theirDerivativesJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
Use of Oximes, Hydroxamic Acids and Related Species as Reagents in Inorganic AnalyticalChemistryJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
Synthesis of Heterocycles from OximesEdmunds LukevicsLatvian Institute of Organic Synthesis, Riga, Latvia LV1006
Synthesis of HydroxylaminesArtem MelmanClarkson University, Department of Chemistry and Biomolecular Science, Potsdam, NY 13699, USA
Some Intrinsic Features of Hydroxylamines, Oximes and Hydroxamic Acids: Integration of Theoryand Experiment
Structural Analysis of Hydroxylamines, Oximes and Hydroxamic Acids: Trends and PatternsJane S. MurrayCleveland State University, Department of Chemistry, Cleveland, OH 44115, USA
Electrochemistry of Hydroxylamines, Oximes and Hydroxamic AcidsOsamu OnomuraNagasaki University, Department of Molecular Medicinal Sciences, Graduate School of BiomedicalSciences, 1–14, Bunkyo-machi, Nagasaki, Japan 852–8521
Rearrangements of Hydroxylamines, Oximes and Hydroxamic AcidsM. Manuela A. PereiraUniversidade Nova de Lisboa, REQUIMTE/CQFB, Departamento de Quımica, Faculdade de Ciencias eTecnologia, Campus da Caparica, Caparica, Portugal 2829-516
183
Some Intrinsic Features of Hydroxylamines, Oximes and Hydroxamic Acids: Integration of Theoryand Experiment
Structural Analysis of Hydroxylamines, Oximes and Hydroxamic Acids: Trends and PatternsPeter PolitzerUniversity of New Orleans, Department of Chemistry, New Orleans, LA 70148, USA
Use of Oximes, Hydroxamic Acids and Related Species as Reagents in Inorganic AnalyticalChemistryMaja PonikvarJozef Stefan Institute, Department of Inorganic Chemistry and Technology, Jamova 39, Ljubljana, SloveniaSI-1000
Synthesis of Oximes and Hydroxamic AcidsAndrea PorchedduUniversita degli Studi di Sassari, Dipartimento di Chimica, via Vienna 2, Sassari, Italy 07100 -
NMR Spectra of Hydroxylamines, Oximes and Hydroxamic AcidsPeter Rudolf SeidlUniversidade Federal do Rio de Janeiro, Centro de Tecnologia, Departamento de Processos Organicos,Escola de Quımica, Bloco E, Ilha do Fundao, Rio de Janeiro, Brazil RJ 21949-900
Rearrangements of Hydroxylamines, Oximes and Hydroxamic AcidsPedro Paulo SantosUniversidade Tecnica de Lisboa, Centro de Quımica Estrutural, Instituto Superior Tecnico, Av. RoviscoPais, Lisboa, Portugal 1049-001
Nitrosomethanides and their Acids: Synthesis, Structure and BondingAxel SchulzUniversitat Rostock, Institut fur Chemie, Abteilung Anorganische Chemie, Albert-Einstein-Straße 3a,Rostock, Germany 18059andLeibniz-Institut fur Katalyse e .V. an der Universitat Rostock, Albert-Einstein-Str. 29a, Rostock, Germany18059
Natural and Biomimetic Hydroxamic Acid Based SiderophoresAbraham ShanzerWeizmann Institute of Science, Department of Organic Chemistry, P.O. Box 26, Rehovot, Israel 76100
Hydroxylamines and Oximes: Biological Properties and Potential Uses as Therapeutic AgentsIsrael SilmanThe Weizmann Institute of Science, Department of Neurobiology, Rehovot, Israel 76100
The Organic Thermochemistry of Hydroxylamines, Oximes, Hydroxamic Acids and theirDerivativesSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA
Hydroxylamine, Oximate and Hydroxamate as α-Nucleophiles in DephosphorylationFrancois TerrierUniversite de Versailles, Institut Lavoisier, 45 Avenue des Etats-Unis 78035, VersaillesCedex, France UMR8180
184
Hydroxylamine, Oximate and Hydroxamate as α-Nucleophiles in DephosphorylationIk Hwan UmEwha Womans University, Division of Nano Sciences and Department of Chemistry, Seoul, Korea 120–750
Nitrosomethanides and their Acids: Synthesis, Structure and BondingAlexander VillingerUniversitat Rostock, Institut fur Chemie, Abteilung Anorganische Chemie, Albert-Einstein-Straße 3a,Rostock, Germany 18059
The Chemistry of Organomagnesium Compounds (2008)Edited by Zvi Rappoport and Ilan Marek
Structural Organomagnesium ChemistryJaap BoersmaFaculty of Science Utrecht University, Chemical Biology & Organic Chemistry, Padualaan 8, Utrecht, CH,The Netherlands 3584
Functionalized Organomagnesium Compounds: Synthesis and ReactivityKatja BradeLudwig-Maximilians-Universitat Munchen, Department Chemie und Biochemie, Butenandtstr. 5–13,Munchen, Germany D-81377
Iron-Catalyzed Reactions of Grignard ReagentsGerard CahiezUMR 8123 CNRS-ESCOM-UCP, Laboratoire de Synthese Organique Selective et de ChimieOrganometallique (SOSCO), 5 Mail Gay Lussac, Cergy-Pontoise, Neuvilles/Oise, France F-95092
Iron-Catalyzed Reactions of Grignard ReagentsChristophe DuplaisUMR 8123 CNRS-ESCOM-UCP, Laboratoire de Synthese Organique Selective et de ChimieOrganometallique (SOSCO), 5 Mail Gay Lussac, Cergy-Pontoise, Neuvilles/Oise, France F-95092
Catalytic Enantioselective Conjugate Addition and Allylic Alkylation Reactions Using GrignardReagentsBen L. FeringaUniversity of Groningen, Stratingh Institute for Chemistry, Nijenborgh 4, Groningen, AG, The Netherlands9747
Functionalized Organomagnesium Compounds: Synthesis and ReactivityAndrey GavryushinLudwig-Maximilians-Universitat Munchen, Department Chemie und Biochemie, Butenandtstr. 5–13,Munchen, Germany D-81377
Preparation and Reactivity of Magnesium EnolatesClaude GrisonUMR CNRS-Universite de Montpellier 2 5032, ENSCM, 8 rue de l’Ecole Normale, Montpellier, FranceF-34296
NMR of Organomagnesium CompoundsPeter J. HeardBirkbeck University of London, School of Biological and Chemical Sciences, Malet Street, London, UKWC1E 7HX
185
Organomagnesium-Group 15- and Organomagnesium-Group 16-Bonded ComplexesKenneth W. HendersonUniversity of Notre Dame, Department of Chemistry and Biochemistry, 251 Nieuwland Science Hall, NotreDame, IN 46556, USA
The Thermochemistry of Organomagnesium CompoundsTorkil HolmTechnical University of Denmark, Department of Chemistry, Building 201, Lyngby, Denmark DK-2800
Organomagnesium-Group 15- and Organomagnesium-Group 16-Bonded ComplexesKatherine L. HullUniversity of Notre Dame, Department of Chemistry and Biochemistry, 251 Nieuwland Science Hall, NotreDame, IN 46556, USA
Carbomagnesiation ReactionsKenichiro ItamiNagoya University, Department of Chemistry and Research Center for Materials Science, Chikusa-ku,Nagoya, Japan 464–8602
Structural Organomagnesium ChemistryJohann T. B. H. JastrzebskiFaculty of Science Utrecht University, Chemical Biology & Organic Chemistry, Padualaan 8, Utrecht, CH,The Netherlands 3584
Electrochemistry of Organomagnesium CompoundsJan S. JaworskiUniversity of Warsaw, Faculty of Chemistry, Warszawa, Poland 02–093
Functionalized Organomagnesium Compounds: Synthesis and ReactivityPaul KnochelLudwig-Maximilians-Universitat Munchen, Department Chemie und Biochemie, Butenandtstr. 5–13,Munchen, Germany D-81377
Structural Organomagnesium ChemistryGerard Van KotenFaculty of Science Utrecht University, Chemical Biology & Organic Chemistry, Padualaan 8, Utrecht, CH,The Netherlands 3584
The Thermochemistry of Organomagnesium CompoundsJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
Catalytic Enantioselective Conjugate Addition and Allylic Alkylation Reactions Using GrignardReagentsFernando LopezUniversidad de Santiago de Compostela, Departamento de Quımica Organica, Facultad de Quımica,Avda. de las ciencias, s/n, Santiago de Compostela, Spain 15782
Catalytic Enantioselective Conjugate Addition and Allylic Alkylation Reactions Using GrignardReagentsAdriaan J. MinnaardUniversity of Groningen, Stratingh Institute for Chemistry, Nijenborgh 4, Groningen, AG, The Netherlands9747
186
Formation, Chemistry and Structure of Organomagnesium Species in Solvent-Free EnvironmentsRichard A. J. O’HairThe University of Melbourne, School of Chemistry, Bio21 Molecular Science and Biotechnology Institute,ARC Centre of Excellence in Free Radical Chemistry and Biotechnology, Victoria, Australia 3010
The Chemistry of Organomagnesium Ate ComplexesKoichiro OshimaKyoto University, Kyoto-daigaku Katsura, Department of Material Chemistry, Graduate School ofEngineering, Kyoto, Nishikyo, Japan 615–8510
The Chemistry of Magnesium CarbenoidsTsuyoshi SatohTokyo University of Science, Department of Chemistry, Faculty of Science, Ichigaya-funagawara-machi 12,Tokyo, Shinjuku-ku, Japan 162–0826
Photochemical Transformations Involving Magnesium Porphyrins and PhthalocyaninesMathias O. SengeTrinityCollegeDublin, School of Chemistry, SFI Tetrapyrrole Laboratory, Dublin 2, Ireland
Photochemical Transformations Involving Magnesium Porphyrins and PhthalocyaninesNatalia N. SergeevaTrinity College Dublin, School of Chemistry, SFI Tetrapyrrole Laboratory, Dublin 2, Ireland
The Thermochemistry of Organomagnesium CompoundsSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA
Biochemistry of MagnesiumJames WestonFriedrich-Schiller-Universitat, Institut fur Organische Chemie und Makromolekulare Chemie,Humboldtstraße 10, Jena, Germany D-07743
Theoretical Studies of the Addition of RMgX to Carbonyl CompoundsShinichi YamabeNara University of Education, Department of Chemistry, Takabatake-cho, Nara, Japan 630–8528
Theoretical Studies of the Addition of RMgX to Carbonyl CompoundsShoko YamazakiNara University of Education, Department of Chemistry, Takabatake-cho, Nara, Japan 630–8528
The Chemistry of Organomagnesium Ate ComplexesHideki YorimitsuKyoto University, Kyoto-daigaku Katsura, Department of Material Chemistry, Graduate School ofEngineering, Kyoto, Nishikyo, Japan 615–8510
Carbomagnesiation ReactionsJun-Ichi YoshidaKyoto University, Graduate School of Engineering, Department of Synthetic Chemistry and BiologicalChemistry, Nishikyo-ku, Kyoto, Japan 615–8510
Analytical Aspects of Organomagnesium CompoundsJacob ZabickyBen-Gurion University of the Negev, Department of Chemical Engineering, P. O. Box 653, Beer-Sheva,Israel 84105
187
The Chemistry of Metal Enolates (2009)Edited by Jacob Zabicky
General and Theoretical Aspects of the Metal EnolatesJuan AndresUniversitat Jaume I, Departament de Quımica Fısica y Analıtica, Castello, Spain 12071
Molecular Structure of Metal EnolatesKsenija Babic-SamardzijaRice University, Chemistry Department, 6100 Main St, Houston, TX 77005, USA andBaker Hughes Incorporateds, 12645 West Airport Blvd, Sugar Land, TX 77478, USA
Analytical Aspects of Metal EnolatesShmuel BittnerBen-Gurion University of the Negev, Department of Chemistry, P. O. Box 653, Beer-Sheva, Israel 84105
Deposition of Metals and Metal Oxides by Means of Metal EnolatesRoy BuschbeckTechnische Universitat Chemnitz, Fakultat fur Naturwissenschaften, Institut fur Chemie, Lehrstuhl furAnorganische Chemie, Strasse der Nationen 62, Chemnitz, Germany 09111
Luminescence Phenomena Involving Metal EnolatesMaria Claudia Franca Cunha FelintoInstitute of Nuclear Energy and Research, Av. Prof Lineu Prestes 2242 Cidade Universitaria, SaoPaulo-SP, Brazil 05508-000
Structure and Properties of d8 Metal–Dithiolene ComplexesPaola DeplanoUniversita di Cagliari, Dipartimento di Chimica Inorganica e Analitica, S.S. 554-Bivio per Sestu,Monserrato-Cagliari, Italy I09042
General and Theoretical Aspects of the Metal EnolatesLuis R. DomingoUniversitat de Valencia, Departament de Quımica Organica, Dr. Moliner 50, Valencia, Spain 46100Burjassot
Acid–Base Properties of Enols and EnolatesJason EamesUniversity of Hull, Department of Chemistry, Cottingham Road, Kingston upon Hull, England HU6 7RX
Luminescence Phenomena Involving Metal EnolatesErcules Epaminondas de Sousa TeotonioFederal University of Goias, Department of Chemistry, Av. Dr. Lamartine P. de Avelar, 1120,Catalao-GO, Brazil 75704-020
Luminescence Phenomena Involving Metal EnolatesHermi Felinto BritoUniversity of Sao Paulo, Department of Fundamental Chemistry, Sao Paulo-SP, Brazil 05508-000
Analytical Aspects of Metal EnolatesEli HarlevBen-Gurion University of the Negev, Department of Chemistry, P. O. Box 653, Beer-Sheva, Israel 84105
188
Metal Enolates in Polymer Science and TechnologyRobert JeromeUniversity of Liege, Center for Education and Research on Macromolecules (CERM), Sart-Tilman, B6a,Liege, Belgium 4000
Molecular Structure of Metal EnolatesVladislava M. JovanovicUniversity of Belgrade, ICTM-Institute of Electrochemistry, Njegoseva 12, P.O. Box 473, Belgrade, Serbia11000
Metal Enolates as Synthons in Organic ChemistryUli KazmaierSaarland University, Department of Organic Chemistry, D-66123 Saarbrucken, Germany
Deposition of Metals and Metal Oxides by Means of Metal EnolatesHeinrich LangTechnische Universitat Chemnitz, Fakultat fur Naturwissenschaften, Institut fur Chemie, Lehrstuhl furAnorganische Chemie, Strasse der Nationen 62, Chemnitz, Germany 09111
Metal Enolates in Polymer Science and TechnologyPhilippe LecomteUniversity of Liege, Center for Education and Research on Macromolecules (CERM), Sart-Tilman, B6a,Liege, Belgium 4000
Joel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
Thermochemical Considerations of Metal Enolates
Luminescence Phenomena Involving Metal EnolatesOscar Manoel Loureiro MaltaFederal University of Pernambuco, CCEN Cidade Universitaria, Department of Fundamental Chemistry,Recife-PE, Brazil 50670-901
Structure and Properties of d8 Metal–Dithiolene ComplexesM. Laura MercuriUniversita di Cagliari, Dipartimento di Chimica Inorganica e Analitica, S.S. 554-Bivio per Sestu,Monserrato-Cagliari, Italy I09042
Biological Aspects of Metal EnolatesLi-June MingUniversity of South Florida, Department of Chemistry and Institute for Biomolecular Science, 4202 E.Fowler Avenue, CHE205, Tampa, FL 33620-5250, USA
Redox Chemistry and Electrochemistry of Metal EnolatesGuido PampaloniUniversita di Pisa, Dipartimento di Chimica e Chimica Industriale, Via Risorgimento 35, Pisa, ItalyI-56126
Structure and Properties of d8 Metal–Dithiolene ComplexesLuca PiliaUniversita di Cagliari, Dipartimento di Chimica Inorganica e Analitica, S.S. 554-Bivio per Sestu,Monserrato-Cagliari, Italy I09042
189
Lanthanide Enolates as Nuclear Magnetic Resonance Shift ReagentsKatelyn A. ProvencherBatesCollege, Department of Chemistry, Lewiston, ME 04240, USA
Structure and Properties of d8 Metal–Dithiolene ComplexesAngela SerpeUniversita di Cagliari, Dipartimento di Chimica Inorganica e Analitica, S.S. 554-Bivio per Sestu,Monserrato-Cagliari, Italy I09042
The Chemistry of Metal YnolatesMitsuru ShindoKyushu University, Institute for Materials, Chemistry and Engineering, Kasuga-koen, Kasuga, Japan816–8580
Thermochemical Considerations of Metal EnolatesSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030-4444, USA
Molecular Structure of Metal EnolatesSofija P. SoviljUniversity of Belgrade, Faculty of Chemistry, Studentski trg 12–16 P.O. Box 158, Belgrade, Serbia 11000
Metal Enolates as Synthons in Organic ChemistryDaniel StolzSaarland University, Department of Organic Chemistry, D-66123 Saarbrucken, Germany
Coordination Chemistry of Metal Enolato Complexes
Synthesis of Metal Enolato ComplexesJose VicenteUniversidad de Murcia, Grupo de Quımica Organometalica, Departamento de Quımica Inorganica,Facultad de Quımica, Apdo. 4021, Murcia, Spain 30071
Lanthanide Enolates as Nuclear Magnetic Resonance Shift ReagentsThomas J. WenzelBates College, Department of Chemistry, Lewiston, ME 04240, USA
Catalysis Using β-Diketonato Metal ComplexesStephen A. WestcottMount Allison University, Department of Chemistry, Sackville, New Brunswick, Canada E4L 1G8
Analytical Aspects of Metal EnolatesJacob ZabickyBen-Gurion University of the Negev, Department of Chemical Engineering, P. O. Box 653, Beer-Sheva,Israel 84105
Redox Chemistry and Electrochemistry of Metal EnolatesPiero ZanelloUniversita di Siena, Dipartimento di Chimica, Via De Gasperi 2, Siena, Italy I-53100
190
The Chemistry of Organocopper Compounds (2009)Edited by Zvi Rappoport and Ilan Marek
Copper-Mediated and Copper-Catalyzed Addition and Substitution Reactions of Extended MultipleBond SystemsOzge Aksin-ArtokDortmund University of Technology, Organic Chemistry II, Otto-Hahn-Strasse 6, Dortmund, GermanyD-44227
Copper-Catalyzed Enantioselective Conjugate AdditionAlexandre AlexakisUniversity of Geneva, Department of Organic Chemistry, 30, quai Ernest Ansermet 1211 Geneve 4,Switzerland
Oxidation of Organocopper CompoundsSarah J. AvesUniversity of Cambridge, Department of Chemistry, Lensfield Road, Cambridge, United Kingdom CB21EW
Silyl and Stannyl Derivatives of Organocopper CompoundsAsuncion BarberoUniversidad de Valladolid, Departamento de Quımica Organica, Facultad de Ciencias, Valladolid, Spain47011
Fluorinated Organocopper ReagentsDonald J. BurtonUniversity of Iowa, Department of Chemistry, Iowa City, IA 52242, USA
Carbocupration of AlkynesFabrice ChemlaUPMC-Univ Paris 6, Institut Parisien de Chimie Moleculaire, CNRS UMR 7201, Tour 44–45, 2 emeEtage,Case 183, 4 Place Jussieu, Paris Cedex 05, France 75252
Fluorinated Organocopper ReagentsCharles R. DavisSigma-Aldrich, 6000 N. Teutonia Avenue, Milwaukee, WI 53209, USA
N-Functionalized OrganocupratesR. Karl DieterClemson University, Howard L. Hunter Laboratory, Department of Chemistry, Clemson, SC 29634-0973,USA
Carbocupration of AlkynesFranck FerreiraUPMC-Univ Paris 6, Institut Parisien de Chimie Moleculaire, CNRS UMR 7201, Tour 44–45, 2 emeEtage,Case 183, 4 Place Jussieu, Paris Cedex 05, France 75252
NMR of Organocopper CompoundsTobias GartnerUniversitat Regensburg, Institut fur Organische Chemie, Universitatsstraße 31, Regensburg, GermanyD-93040
191
Copper-Mediated Cross-Coupling ReactionsDmitri GelmanThe Hebrew University of Jerusalem, Institute of Chemistry, Edmund Safra Campus, Givat Ram,Jerusalem, Israel 91904
Biochemistry of Organocopper CompoundsSaul Gomez-ManzoUniversidad Nacional Autonoma de Mexico, Facultad de Quımica, Ciudad Universitaria, Coyoacan, D.F.Mexico, Mexico 04510
NMR of Organocopper CompoundsRuth M. GschwindUniversitat Regensburg, Institut fur Organische Chemie, Universitatsstraße 31, Regensburg, GermanyD-93040
Structural Organocopper ChemistryJohann T. B. H. JastrzebskiUtrecht University, Chemical Biology & Organic Chemistry, Debye Institute for Nanomaterials Science,Faculty of Science, Padualaan 8, Utrecht, The Netherlands 3584 CH
Electrochemistry of Organocopper CompoundsJan S. JaworskiUniversity of Warsaw, Faculty of Chemistry, Warszawa, Poland 02–093
Structural Organocopper ChemistryGerard van KotenUtrecht University, Chemical Biology & Organic Chemistry, Debye Institute for Nanomaterials Science,Faculty of Science, Padualaan 8, Utrecht, The Netherlands 3584 CH
Copper-Mediated and Copper-Catalyzed Addition and Substitution Reactions of Extended MultipleBond SystemsNorbert KrauseDortmund University of Technology, Organic Chemistry II, Otto-Hahn-Strasse 6, Dortmund, GermanyD-44227
Biochemistry of Organocopper CompoundsPeter M. H. KroneckUniversitat Konstanz, Fachbereich Biologie, Konstanz, Germany 78457
Gas-Phase Chemistry of Organocopper CompoundsAl Mokhtar LamsabhiUniversidad Autonoma de Madrid, Departamento de Quımica, Cantoblanco, Madrid, Spain 28049
Thermochemistry of Organocopper CompoundsJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
Theory of Organocopper-Mediated ReactionsEiichi NakamuraThe University of Tokyo, Department of Chemistry, Hongo, Bunkyo-ku, Tokyo, Japan 113-0033
192
Copper-Mediated Cross-Coupling ReactionsLiza PennThe Hebrew University of Jerusalem, Institute of Chemistry, Edmund Safra Campus, Givat Ram,Jerusalem, Israel 91904
Copper-Catalyzed Enantioselective Conjugate AdditionDamien PoletUniversity of Geneva, Department of Organic Chemistry, 30, quai Ernest Ansermet 1211 Geneve 4,Switzerland
Silyl and Stannyl Derivatives of Organocopper CompoundsFrancisco J. PulidoUniversidad de Valladolid, Departamento de Quımica Organica, Facultad de Ciencias, Valladolid, Spain47011
Copper(I) Hydride Reagents and CatalystsOlivier RiantUniversite catholique de Louvain, Unite de chimie organique et medicinale, departement de chimie, PlaceLouis Pasteur 1, Louvain la Neuve, Belgium 1348
Transmetalation Reactions Producing Organocopper CompoundsChristopher J. RosenkerUniversity of Pittsburgh, Department of Chemistry, Pittsburgh, PA 15260, USA
Gas-Phase Chemistry of Organocopper CompoundsJean-Yves SalpinUniversite d’Evry Val d’Essonne, Laboratoire d’Analyse et Modelisation pour la Biologie etl’Environnement-CNRS, UMR 8587—Batiment Maupertuis, Boulevard Francois Mitterrand, Evry, France91025
Biochemistry of Organocopper CompoundsJuan P. Saucedo-VazquezUniversidad Nacional Autonoma de Mexico, Facultad de Quımica, Ciudad Universitaria, Coyoacan, D.F.Mexico, Mexico 04510
Photochemical Transformations Involving Copper Porphyrins and PhthalocyaninesMathias O. SengeTrinity College Dublin, School of Chemistry, SFI Tetrapyrrole Laboratory, Dublin 2, Ireland andSt. James’s Hospital, TrinityCollegeDublin, Institute of Molecular Medicine, Medicinal Chemistry, TrinityCentre for Health Sciences, Dublin 8, Ireland
Photochemical Transformations Involving Copper Porphyrins and PhthalocyaninesNatalia N. SergeevaTrinityCollegeDublin, School of Chemistry, SFI Tetrapyrrole Laboratory, Dublin 2, Ireland
Thermochemistry of Organocopper CompoundsSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA
Biochemistry of Organocopper CompoundsMartha E. Sosa-TorresUniversidad Nacional Autonoma de Mexico, Facultad de Quımica, Ciudad Universitaria, Coyoacan, D.F.Mexico, Mexico 04510
193
Copper-Mediated Asymmetric Allylic AlkylationsClaude SpinoUniversite de Sherbrooke, Departement de Chimie, Sherbrooke, Quebec, Canada J1K 2R1
Oxidation of Organocopper CompoundsDavid R. SpringUniversity of Cambridge, Department of Chemistry, Lensfield Road, Cambridge, United KingdomCB21EW
Gas-Phase Chemistry of Organocopper CompoundsJeanine TortajadaUniversite d’Evry Val d’Essonne, Laboratoire d’Analyse et Modelisation pour la Biologie etl’Environnement-CNRS, UMR 8587—Batiment Maupertuis, Boulevard Francois Mitterrand, Evry, France91025
N-Functionalized OrganocupratesRhett T. WatsonUniversity of South Carolina Upstate, Division of Natural Sciences and Engineering, 800 University Way,Spartanburg, SC 29303, USA
Transmetalation Reactions Producing Organocopper CompoundsPeter WipfUniversity of Pittsburgh, Department of Chemistry, Pittsburgh, PA 15260, USA
Gas-Phase Chemistry of Organocopper CompoundsManuel YanezUniversidad Autonoma de Madrid, Departamento de Quımica, Cantoblanco, Madrid, Spain 28049
Theory of Organocopper-Mediated ReactionsNaohiko YoshikaiThe University of Tokyo, Department of Chemistry, Hongo, Bunkyo-ku, Tokyo, Japan 113-0033
The Chemistry of Hydroxylamines, Oximes and Hydroxamic Acids, Volume 2 (2010)(See Volume 1 in 2008)
Edited by Zvi Rappoport and Joel F. Liebman
Synthesis, structure and reactions of organometallic derivatives of oximesEdgars AbeleLatvian Institute of Organic Synthesis, Riga, LV1006, Latvia
N-Hydroxylamines for peptide synthesisFernando AlbericioInstitute for Research in Biomedicine, BarcelonaSciencePark, Baldiri Reixac 10, 08028-Barcelona, Spain,Biomaterials and Nanomedicine, CIBER-BBN, Networking Centre on Bioengineering,BarcelonaSciencePark, Baldiri Reixac 10, 08028-Barcelona, Spain andUniversity of Barcelona, Martı i Franques 1–11, Department of Organic Chemistry, 08028-Barcelona,Spain
Phosphorus derivatives of hydroxylamines, oximes and hydroxamic acidsConcepcion AlonsoFacultad de Farmacia, Universidad del Paıs Vasco, Departamento de Quımica Organica I, Apartado 450,01080 Vitoria Spain
194
The Brønsted acid/base character of hydroxylamines, oximes and hydroxamic acidsJohn E. BartmessUniversity of Tennessee, Department of Chemistry, Knoxville, TN 37996 1600, USA
Diazohydroxides, diazoethers and related speciesCarlos D. Bravo-dıazUniversidad de Vigo, Fac. Quımica, Dpto. Quımica, Fısica, 36 310 Vigo, Pontevedra, Spain
N-Arylhydroxylamines and chemical carcinogenicityMrinal ChakrabortyMiami University, Department of Chemistry and Biochemistry, Oxford, OH45056, USA
Properties, structure and reactivity of cobaloximesRenata DreosUniversita degli Studi di Trieste, Dipartimento di Scienze Chimiche, 34127 Trieste, Italy
Conjugate addition of hydroxylamines, oximes and hydroxamic acidsYunfei DuSchool of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District,Tianjin, Peoples’ Republic of China 300072
N-Hydroxylamines for peptide synthesisAyman El-FahamAlexandria University, Faculty of Science, Department of Chemistry, P.O. Box 246, Ibrahimia, 21321Alexandria, Egypt
The chemistry of NO- and HNO-producing diazeniumdiolatesAnthony S. EvansJohns Hopkins University, Department of Chemistry, Baltimore, MD 21218, USA
Properties, structure and reactivity of cobaloximesSilvano GeremiaUniversita degli Studi di Trieste, Dipartimento di Scienze Chimiche, 34127 Trieste, Italy
Mass spectrometry of hydroxylamines, oximes and hydroxamic acidsGianluca GiorgiDepartment of Chemistry, University of Siena, Via Aldo Moro I-53100 Siena, Italy
Peroxynitrogen: A study of nitrogen/oxygen heterocycles with N–O and O–O or N–O–O bondingAlexander GreerDepartment of Chemistry, Graduate Center and CUNY, Brooklyn College, 2900 Bedford Ave., Brooklyn,NY 11210, USA
Heterocycles from hydroxylamines and hydroxamic acidsMartins KatkevicsLatvian Institute of Organic Synthesis, Riga, Latvia LV1006
Hydroxylamine, oxime and hydroxamic acid derivatives of nucleic acidsNaoshi KojimaBioproduction Research Institute, National Institute of Advanced Industrial Science and Technology(AIST), 2-17-2-1 Tsukisamu-Higashi, Toyohira-ku, Sapporo 062–8517, Japan
195
Hydroxylamine, oxime and hydroxamic acid derivatives of nucleic acidsYasuo KomatsuBioproduction Research Institute, National Institute of Advanced Industrial Science and Technology(AIST), 2-17-2-1 Tsukisamu-Higashi, Toyohira-ku, Sapporo 062–8517, Japan
Heterocycles from hydroxylamines and hydroxamic acidsTatyana KukoshaLatvian Institute of Organic Synthesis, Riga, Latvia LV1006
Peroxynitrogen: A study of nitrogen/oxygen heterocycles with N–O and O–O or N–O–O bondingJoel F. LiebmanDepartment of Chemistry and Biochemistry, University of Maryland Baltimore County, 1000 HilltopCircle, Baltimore, MD 21250, USA
Heterocycles from hydroxylamines and hydroxamic acids
Synthesis, structure and reactions of organometallic derivatives of oximesEdmunds LukevicsLatvian Institute of Organic Synthesis, Riga, LV1006, Latvia
Hydroxamic acids: Biological properties and potential uses as therapeutic agentsAntonello MaiSapienza University of Rome, Pasteur Institute—Cenci Bolognetti Foundation, Department of DrugChemistry and Technologies, P.le A. Moro 5, 00185 Rome, Italy
Conjugate addition of hydroxylamines, oximes and hydroxamic acidsDeng MaoSchool of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District,Tianjin, Peoples’ Republic of China 300072
N-Arylhydroxylamines and chemical carcinogenicityMichael NovakMiami University, Department of Chemistry and Biochemistry, Oxford, OH 45056, USA
Phosphorus derivatives of hydroxylamines, oximes and hydroxamic acidsFrancisco PalaciosFacultad de Farmacia, Universidad del Paıs Vasco, Departamento de Quımica Organica I, Apartado 450,01080 Vitoria Spain
Properties, structure and reactivity of cobaloximesLucio RandaccioUniversita degli Studi di Trieste, Dipartimento di Scienze Chimiche, 34127 Trieste, Italy
Light-induced chemistry of oximes and derivativesHeinz D. RothRutgers University, Department of Chemistry and Chemical Biology, New Brunswick, NJ 08854 0939, USA
Phosphorus derivatives of hydroxylamines, oximes and hydroxamic acidsJesus M. de los SantosFacultad de Farmacia, Universidad del Paıs Vasco, Departamento de Quımica Organica I, Apartado 450,01080 Vitoria Spain
196
Properties, structure and reactivity of cobaloximesPatrizia SiegaUniversita degli Studi di Trieste, Dipartimento di Scienze Chimiche, 34127 Trieste, Italy
Peroxynitrogen: A study of nitrogen/oxygen heterocycles with N–O and O–O or N–O–O bondingSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax, VA 22030, USA
N-Hydroxylamines for peptide synthesisRamon Subiros-FunosasInstitute for Research in Biomedicine, BarcelonaSciencePark, Baldiri Reixac 10, 08028-Barcelona, Spain
The chemistry of NO- and HNO-producing diazeniumdiolatesJohn P. ToscanoJohns Hopkins University, Department of Chemistry, Baltimore, MD 21218, USA
Phosphorus derivatives of hydroxylamines, oximes and hydroxamic acidsJavier VicarioFacultad de Farmacia, Universidad del Paıs Vasco, Departamento de Quımica Organica I, Apartado 450,01080 Vitoria Spain
Conjugate addition of hydroxylamines, oximes and hydroxamic acidsDaisy Zhang-NegrerieSchool of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District,Tianjin, Peoples’ Republic of China 300072
Conjugate addition of hydroxylamines, oximes and hydroxamic acidsKang ZhaoSchool of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District,Tianjin, Peoples’ Republic of China 300072
Hydroxylamine analogs and derivatives of amino acids. Aminooxy acidsGury ZvilichovskyInstituteof Chemistry, The Hebrew University of Jerusalem, Jerusalem91904, Israel
The Chemistry of Organomanganese Compounds (2011)Edited by Zvi Rappoport and Ilan Marek
Manganese in Biological Systems: Transport and FunctionNoam AdirSchulich Faculty of Chemistry, Technion—Israel Institute of Technology, Haifa, Israel 32000
Preparation and Reactivity of Organomanganese CompoundsGerard CahiezLaboratoire de Synthese Organique Selective et de Chimie Organometallique (SOSCOM), FRE 3043CNRS-Universite Paris13, 74 rue Marcel Cachin, Bobigny, France F-93017
Catalytic Enantioselective Reactions using Organomanganese CompoundsNicka ChinkovFaculty of Natural Sciences, Department of Biology and Environment, University of Haifa, Oranim, KiryatTivon, Israel 36006
197
The Chemistry of Manganese EnolatesJose M. ConcellonUniversidad de Oviedo, Departamento de Quımica Organica e Inorganica, Facultad de Quımica, JulianClaverıa 8, Oviedo, Spain 33 071
The Chemistry of Manganese EnolatesVicente Del AmoUniversidad de Oviedo, Departamento de Quımica Organica e Inorganica, Facultad de Quımica, JulianClaverıa 8, Oviedo, Spain 33 071
Cationic (η6-arene)- and Neutral (η5-cyclohexadienyl)-tricarbonylmanganese Complexes: Synthesisand ReactivityAntoine EloiUniversite Pierre et Marie Curie, UPMC Paris 6, IPCM, UMR CNRS 7201, Laboratoire de ChimieOrganique et Organometallique, Case 181, 4 place Jussieu, Paris Cedex 05, France F-75252
Organomanganese-Mediated Radical ReactionsGregory K. FriestadUniversity of Iowa, Department of Chemistry, Iowa City, IA 52 242, USA
Preparation and Reactivity of Organomanganese CompoundsOlivier GagerLaboratoire de Synthese Organique Selective et de Chimie Organometallique (SOSCOM), FRE 3043CNRS-Universite Paris13, 74 rue Marcel Cachin, Bobigny, France F-93017
Structural Organomanganese ChemistryTimothy P. HanusaVanderbilt University, Department of Chemistry, Nashville, TN 37235, USA
Manganese in Biological Systems: Transport and FunctionMargarita KanteevSchulich Faculty of Chemistry, Technion—IsraelInstitute of Technology, Haifa, Israel 32000
Manganese in Biological Systems: Transport and FunctionNir KerenDepartment of Plant and Environmental Sciences, Silberman Institute of Life sciences, The HebrewUniversity of Jerusalem, Edmond J. Safra Campus, Givat-Ram, Jerusalem, Israel 91904
s-Block-Metal-Mediated Manganation ReactionsRichard A. LayfieldThe University of Manchester, School of Chemistry, Oxford Road, Manchester, UK M13 9PL
Structures and Reaction Mechanisms of Manganese OxidantsDonald G. LeeUniversity of Regina, Department of Chemistry and Biochemistry, Regina, Saskatchewan, Canada S4S 1P2
Structure and Bonding of Simple Manganese-Containing CompoundsJerzy LeszczynskiDepartment of Chemistry and Interdisciplinary Center for Nanotoxicity, Jackson State University, Jackson,MS 39217, USA
198
Energetics of Organomanganese CompoundsJoel F. LiebmanUniversity of Maryland Baltimore County, Department of Chemistry and Biochemistry, 1000 HilltopCircle, Baltimore, MD 21250, USA
Structure and Bonding of Simple Manganese-Containing CompoundsDevashis MajumdarDepartment of Chemistry and Interdisciplinary Center for Nanotoxicity, Jackson State University, Jackson,MS 39217, USA
Structural Organomanganese ChemistryRyan M. MeierVanderbilt University, Department of Chemistry, Nashville, TN 37235, USA
Structure and Bonding of Simple Manganese-Containing CompoundsMinh Tho NguyenDepartment of Chemistry, Katholieke Universiteit Leuven, B-3001 Leuven, Belgium
The Chemistry of Organomanganese Ate ComplexesKoichiro OshimaKyoto University, Department of Material Chemistry, Graduate School of Engineering, Kyoto-daigakuKatsura, Nishikyo-ku, Kyoto, Japan 615–8510
Mass Spectrometry and Gas-Phase Ion Chemistry of Organomanganese ComplexesSergiu P. PaliiUniversity of Florida, Biomedical Mass Spectrometry Laboratory, Clinical Research Center, Gainesville,FL 32610 0322, USA
The Chemistry of Manganese EnolatesHumberto Rodrıguez-SollaUniversidad de Oviedo, Departamento de Quımica Organica e Inorganica, Facultad de Quımica, JulianClaverıa 8, Oviedo, Spain 33 071
Cationic (η6-arene)- and Neutral (η5-cyclohexadienyl)-tricarbonylmanganese Complexes: Synthesisand ReactivityEric RoseUniversite Pierre et Marie Curie, UPMC Paris 6, IPCM, UMR CNRS 7201, Laboratoire de ChimieOrganique et Organometallique, Case 181, 4 place Jussieu, Paris Cedex 05, France F-75252
Cationic (η6-arene)- and Neutral (η5-cyclohexadienyl)-tricarbonylmanganese Complexes: Synthesisand ReactivityFrancoise Rose-MunchUniversite Pierre et Marie Curie, UPMC Paris 6, IPCM, UMR CNRS 7201, Laboratoire de ChimieOrganique et Organometallique, Case 181, 4 place Jussieu, Paris Cedex 05, France F-75252
Structure and Bonding of Simple Manganese-Containing CompoundsSzczepan RoszakInstitute of Physical and Theoretical Chemistry, Wroclaw University of Technology, 50–370 Wroclaw,Poland
Manganese in Biological Systems: Transport and FunctionEitan SalomonDepartment of Plant and Environmental Sciences, Silberman Institute of Life sciences, The HebrewUniversity of Jerusalem, Edmond J. Safra Campus, Givat-Ram, Jerusalem, Israel 91904
199
Energetics of Organomanganese CompoundsSuzanne W. SlaydenDepartment of Chemistry George Mason University, 4400 University Drive, Fairfax, VA 22030, USA
The Chemistry of Organomanganese Ate ComplexesHideki YorimitsuKyoto University, Department of Chemistry, Graduate School of Science, Kitashirakawa, Sakyo-ku, Kyoto,Japan 606–8502
Mass Spectrometry and Gas-Phase Ion Chemistry of Organomanganese ComplexesDmitri V. ZagorevskiiCenter for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, 1145 CBIS, 1108th Str., Troy, NY 12180, USA
The Chemistry of Organic Selenium and Tellurium Compounds, Volume 3 (2012)(See Volume 1 in 1986, Volume 2 in 1987)
Edited by Zvi Rappoport
Advances in Free Radical Reactions of Organoselenium and Organotellurium CompoundsThomas G. BackUniversity of Calgary, Department of Chemistry, Calgary, Alberta, Canada, T2N 1N4
The Chemistry of SelenocysteineJoris BeldLaboratory of Organic Chemistry, ETH Zurich, Zurich, Switzerland
Selenium- and Tellurium-Containing Organic π-Conjugated Oligomers and PolymersMichael BendikovWeizmann Institute of Science, Department of Organic Chemistry, Rehovot, Israel 76100
Biological and Biochemical Aspects of Tellurium DerivativesMichael R. DettyDepartment of Chemistry, University at Buffalo, Buffalo, NY 14260 3000, USA
Functional Groups Containing Selenium and Tellurium in Oxidation States from 3 to 6
Hypervalent Derivatives of Selenium and Tellurium
Selenium and Tellurium (1,2,3)-Oxygen-containing Acids and DerivativesJozef DrabowiczCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90–363Lodz, Poland andJanDlugosz University in Czestochowa, Department of Chemistry, Environment Protection andBiotechnology, 42-200-Czestochowa, Armii Krajowej Ave. 13/15, Poland
Recent Advances in Analytical Chemistry and Mass Spectrometry for Organic Selenium andTellurium CompoundsGauthier EppeInorganic Analytical Chemistry, University of Liege, 3, Laboratory of Mass Spectrometry, Allee de laChimie B6C, Liege, Belgium 4000
200
Recent Advances in Analytical Chemistry and Mass Spectrometry for Organic Selenium andTellurium CompoundsJohann FarInorganic Analytical Chemistry, University of Liege, 3, Laboratory of Mass Spectrometry, Allee de laChimie B6C, Liege, Belgium 4000
The Chemistry of SelenocysteineDonald HilvertLaboratory of Organic Chemistry, ETH Zurich, Zurich, Switzerland
Electrochemistry of Organic Selenium and Tellurium CompoundsJan S. JaworskiFaculty of Chemistry, University of Warsaw, Warszawa, Poland 02–093
Compounds of Selenium and Tellurium with Nitrogen BondsThomas M. KlapotkeLudwig-Maximilians University of Munich, Department of Chemistry, Butenandtstr. 5–13(D), D-81377Munich, Germany
Functional Groups Containing Selenium and Tellurium in Oxidation States from 3 to 6
Hypervalent Derivatives of Selenium and TelluriumPiotr KiełbasinskiCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90–363Lodz, Poland
Selenium and Tellurium (1,2,3)-Oxygen-containing Acids and DerivativesDorota KrasowskaCentre of Molecular and Macromolecular Studies, PolishAcademy of Sciences, Sienkiewicza 112, Lodz,Poland 90–363
Compounds of Selenium and Tellurium with Nitrogen BondsBurkhard KrummLudwig-Maximilians University of Munich, Department of Chemistry, Butenandtstr. 5–13(D), D-81377Munich, Germany
Aspects of the Chemistry of Species with Carbon–Polonium Bonds
Thermochemistry of Organoselenium and Organotellurium CompoundsJoel F. LiebmanUniversity of Maryland, Baltimore County (UMBC), Department of Chemistry and Biochemistry, 1000Hilltop Circle, Baltimore MD 21250, USA
Organoselenium and Organotellurium Oxidation and ReductionRafał LisiakWrocław University of Technology, Department of Organic Chemistry, Faculty of Chemistry, WybrzezeWyspianskiego 27, Wrocław, Poland 50 370
Substituent Constants and Substituent Effects in Organoselenium and Organotellurium CompoundsMargaret E. LoganThe College at Brockport, Department of Chemistry, SUNY, Brockport, NY 14420, USA
201
Theoretical and Computational Aspects of Organotellurium CompoundsRicardo L. LongoUniversidade Federal de Pernambuco, Cidade Universitaria, Departamento de Quımica Fundamental,Recife, PE, Brazil 50740-540
Theoretical and Computational Aspects of Organotellurium CompoundsPaulo H. MenezesUniversidade Federal de Pernambuco, Cidade Universitaria, Departamento de Quımica Fundamental,Recife, PE, Brazil 50740-540
Vinyl Selenides
Vinylic TelluridesPaulo Henrique MenezesUniversidade Federal de Pernambuco, Departamento Quımica Fundamental, Recife, PE, Brazil 50670-901
The Chemistry of SelenocysteineNorman MetanisLaboratory of Organic Chemistry, ETH Zurich, Zurich, Switzerland
Functional Groups Containing Selenium and Tellurium in Oxidation States from 3 to 6Wanda H. MiduraCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90–363Lodz, Poland
Selenium and Tellurium (1,2,3)-Oxygen-containing Acids and DerivativesWanda Halina MiduraCentre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, Lodz,Poland 90–363
Organoselenium and Organotellurium Oxidation and ReductionJacek MłochowskiWrocław University of Technology, Department of Organic Chemistry, Faculty of Chemistry, WybrzezeWyspianskiego 27, Wrocław, Poland 50 370
Compounds of Selenium and Tellurium with Nitrogen BondsRichard MollLudwig-Maximilians University of Munich, Department of Chemistry, Butenandtstr. 5–13(D), D-81377Munich, Germany
Organotellurium Compounds as Chain Transfer agents for Living Radical PolymerizationYasuyuki NakamuraInstitute for Chemical Research, Kyoto University, Uji, Kyoto, Japan 611-0011
Organoselenium and organotellurium compounds: Toxicology and pharmacologyCristina W. NogueiraLaboratorio de Sıntese, Reatividade e Avaliacao Farmacologica e Toxicologica de Organocalcogenios,CCNE, UFSM, Santa Maria, RS, Brazil CEP 97105-900
Preparative Uses of Organoselenium and Organotellurium CompoundsAkihiro NomotoGraduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Department of AppliedChemistry, Naka-ku, Sakai, Osaka 599–8531, Japan
202
Preparative Uses of Organoselenium and Organotellurium CompoundsAkiya OgawaGraduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Department of AppliedChemistry, Naka-ku, Sakai, Osaka 599–8531, Japan
Selenium- and Tellurium-Containing Organic π-Conjugated Oligomers and PolymersAsit PatraWeizmann Institute of Science, Department of Organic Chemistry, Rehovot, Israel 76100
Recent Advances in Analytical Chemistry and Mass Spectrometry for Organic Selenium andTellurium CompoundsEdwin De PauwInorganic Analytical Chemistry, University of Liege, 3, Laboratory of Mass Spectrometry, Allee de laChimie B6C, Liege, Belgium 4000
Aspects of the Chemistry of Species with Carbon–Polonium BondsMaja Ponikvar-SvetJozef Stefan Institute,, Department of Inorganic Chemistry and Technology, Jamova 39, SI-1000 Ljubljana,Slovenia
Advances in Free Radical Reactions of Organoselenium and Organotellurium CompoundsDavid J. PressUniversity of Calgary, Department of Chemistry, Calgary, Alberta, Canada, T2N 1N4
Organoselenium and organotellurium compounds: Toxicology and pharmacologyJoao B. T. RochaLaboratorio de Sıntese, Reatividade e Avaliacao Farmacologica e Toxicologica de Organocalcogenios,CCNE, UFSM, Santa Maria, RS, Brazil CEP 97105-900
Stereoselective Reactions of Organoselenium Reagents Including CatalysisFateh V. SinghSchoolof Chemistry, Cardiff University, Park Place, Cardiff, UKCF10 3AT
Thermochemistry of Organoselenium and Organotellurium CompoundsSuzanne W. SlaydenGeorge Mason University, Department of Chemistry, 4400 University Drive, Fairfax VA 22030, USA
Theoretical Aspects of Organoselenium ChemistryRaghavan B. SunojIndian Institute of Technology Bombay, Department of Chemistry, Powai, Mumbai, India 400076
Stereoselective Reactions of Organoselenium Reagents Including CatalysisThomas WirthSchoolof Chemistry, Cardiff University, Park Place, Cardiff, UK CF10 3AT
Organoselenium and Organotellurium Oxidation and ReductionHalina Wojtowicz-MłochowskaWrocław University of Technology, Department of Organic Chemistry, Faculty of Chemistry, WybrzezeWyspianskiego 27, Wrocław, Poland 50 370
Organotellurium Compounds as Chain Transfer agents for Living Radical PolymerizationShigeru YamagoInstitute for Chemical Research, Kyoto University, Uji, Kyoto, Japan 611-0011
203
Hypervalent Derivatives of Selenium and TelluriumAdrian ZajacPolishAcademy of Sciences, Centre of Molecular and Macromolecular Studies, Sienkiewicza 112, Lodz,Poland 90–363
Vinyl Selenides
Vinylic TelluridesGilson ZeniUniversidade Federal de Santa Maria, Departamento de Quımica, Santa Maria, RS, Brazil 97105-900
204
