ChemInform Abstract: Site-Selective Suzuki—Miyaura Cross-Coupling Reactions of...
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ChemInform 2011, 42, issue 21 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Furan derivatives R 0060 DOI: 10.1002/chin.201121101 Site-Selective Suzuki—Miyaura Cross-Coupling Reactions of 2,3,4,5-Tetrabro- mofuran. — Procedures are developed for a selective preparation of mono-, bis- and symmetrical and unsymmetrical tetra-arylated furan derivatives. The stoichiometry and the choice of the solvents is crucial for the reaction outcome. Naphthylboronic acid fails to react. — (HUSSAIN, M.; KHERA, R. A.; HUNG, N. T.; LANGER*, P.; Org. Biomol. Chem. 9 (2011) 2, 370-373, http://dx.doi.org/10.1039/c0ob00695e ; Leibniz-Inst. Katal., Univ. Rostock, D-18059 Rostock, Germany; Eng.) — Y. Steudel 21- 101
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Transcript of ChemInform Abstract: Site-Selective Suzuki—Miyaura Cross-Coupling Reactions of...
Furan derivativesR 0060 DOI: 10.1002/chin.201121101
Site-Selective Suzuki—Miyaura Cross-Coupling Reactions of 2,3,4,5-Tetrabro-mofuran. — Procedures are developed for a selective preparation of mono-, bis- and symmetrical and unsymmetrical tetra-arylated furan derivatives. The stoichiometry and the choice of the solvents is crucial for the reaction outcome. Naphthylboronic acid fails to react. — (HUSSAIN, M.; KHERA, R. A.; HUNG, N. T.; LANGER*, P.; Org. Biomol. Chem. 9 (2011) 2, 370-373, http://dx.doi.org/10.1039/c0ob00695e ; Leibniz-Inst. Katal., Univ. Rostock, D-18059 Rostock, Germany; Eng.) — Y. Steudel
21- 101
ChemInform 2011, 42, issue 21 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
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