Rapid, Efficient and Chemoselective Deoxygenation of Sulfoxides to Thioethers Using NaBH4/I2.

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2003 Thioethers Thioethers Q 0580 Rapid, Efficient and Chemoselective Deoxygenation of Sulfoxides to Thioethers Using NaBH 4 /I 2 . — (KARIMI*, B.; ZAREYEE, D.; Synthesis 2003, 3, 335-336; Dep. Chem., Inst. Adv. Stud. Basic Sci., Gava Zang, Zanjan, Iran; Eng.) — C. Herrmann 25- 111

Transcript of Rapid, Efficient and Chemoselective Deoxygenation of Sulfoxides to Thioethers Using NaBH4/I2.

Page 1: Rapid, Efficient and Chemoselective Deoxygenation of Sulfoxides to Thioethers Using NaBH4/I2.

2003 Thioethers

ThioethersQ 0580 Rapid, Efficient and Chemoselective Deoxygenation of Sulfoxides to Thioethers

Using NaBH4/I2. — (KARIMI*, B.; ZAREYEE, D.; Synthesis 2003, 3, 335-336; Dep. Chem., Inst. Adv. Stud. Basic Sci., Gava Zang, Zanjan, Iran; Eng.) —C. Herrmann

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Butanone is reduced in a two-step reaction using NaBH4 ...

Butanone is reduced in a two-step reaction using NaBH4 ...

NaBH4 Reduction of p-Vanillin

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Unexpected Cleavage of Thiacalix[4]arene Sulfoxides · Unexpected Cleavage of Thiacalix[4]arene Sulfoxides Jiří Mikšátko†, Václav Eigner,§ and Pavel Lhoták†* †Department

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Asymmetric synthesis of tertiary thiols and thioethers methods available for the asymmetric synthesis of chiral tertiary thiols and their sulfur(II) derivatives. Two general approaches

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Kemira Sodium Borohydride NaBH4 An effective reducing agent Brochure.pdf · The rate of reduction ... water accelerates the hydrolysis reaction. Sodium Borohydride NaBH 4 – Powder,

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attempts to obtain optically active trifloromethyl aryl sulfoxides

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Reduction of Aldehydes and Ketones using NaBH4 or LiAlH4home.cc.umanitoba.ca/~hultin/chem2220/Support/Reduction_of_Carbonyl... · Reduction of Aldehydes and Ketones using NaBH 4 or

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Protein Engineering of Toluene Monooxygenases …...Protein Engineering of Toluene Monooxygenases for Synthesis of Chiral Sulfoxides Roi Feingersch, 1Janna Shainsky, Thomas K. Wood,2

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Efficient Synthesis of Unsymmetrical Heteroaryl Thioethers and … · 2016-06-07 · 1.2 equiv.), and sodium hydroxide (30.0 mg, 0.75 mmol, 1.5 equiv.) in dimethyl sulfoxide (1.0

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ntur.lib.ntu.edu.twntur.lib.ntu.edu.tw/bitstream/246246/170939/1/51.pdfallylic alcohols. Sulfoxides are intrinsically chiral reagents and their use in asymmetric control is well documented.'

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Index [application.wiley-vch.de] · alkyl trifluoromethyl (or perfluoroalkyl) sulfoximines 681 alkyl trifluoromethyl sulfoxides [(Alk) S(O)CF 3] applications 491–492 preparation

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1 Asymmetric Synthesis of Chiral Sulfoxides - Wiley-VCH · 6 1 Asymmetric Synthesis of Chiral Sulfoxides. 1.2.3 Sulfinates from Sulfites Dissymmetrical sulfites have a stereogenic

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Thiolactone Sulfoxides as New Reactive Metabolites Acting ...courses.washington.edu/medch582/PDFs/pdfarchive/2013May...2013/05/13  · characterization of the corresponding adducts

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A Concise Review on Synthesis of Sulfoxides and …...synthesize the sulfoxides or sulfones, oxidation of sulfide is the most convenient way. This review precises chemoselective methods

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