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ChemInform 2011, 42, issue 10 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Polyphenyl derivatives Q 0700 DOI: 10.1002/chin.201110089 Pd-Catalyzed Coupling of Aryl Iodides with Triarylbismuths as Atom-Economic Multi-Coupling Organometallic Nucleophiles under Mild Conditions. — The op- timized conditions allow the preparation of a broad spectrum of mixed biaryls. The in- vestigation of a multicoupling version produces amines of type (XII) with moderate yields due to formation of biaryls as by-products. — (RAO*, M. L. N.; BANERJEE, D.; DHANORKAR, R. J.; Tetrahedron Lett. 51 (2010) 47, 6101-6104, http://dx.doi.org/10.1016/j.tetlet.2010.09.053 ; Dep. Chem., Indian Inst. Technol., Kanpur 208 016, India; Eng.) — Mais 10- 089

ChemInform Abstract: Pd-Catalyzed Coupling of Aryl Iodides with Triarylbismuths as Atom-Economic Multi-Coupling Organometallic Nucleophiles under Mild Conditions

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Page 1: ChemInform Abstract: Pd-Catalyzed Coupling of Aryl Iodides with Triarylbismuths as Atom-Economic Multi-Coupling Organometallic Nucleophiles under Mild Conditions

Polyphenyl derivativesQ 0700 DOI: 10.1002/chin.201110089

Pd-Catalyzed Coupling of Aryl Iodides with Triarylbismuths as Atom-Economic Multi-Coupling Organometallic Nucleophiles under Mild Conditions. — The op-timized conditions allow the preparation of a broad spectrum of mixed biaryls. The in-vestigation of a multicoupling version produces amines of type (XII) with moderate yields due to formation of biaryls as by-products. — (RAO*, M. L. N.; BANERJEE, D.; DHANORKAR, R. J.; Tetrahedron Lett. 51 (2010) 47, 6101-6104, http://dx.doi.org/10.1016/j.tetlet.2010.09.053 ; Dep. Chem., Indian Inst. Technol., Kanpur 208 016, India; Eng.) — Mais

10- 089

ChemInform 2011, 42, issue 10 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim