4.8 Article

Ni-Catalyzed Sonogashira Coupling of Nonactivated Alkyl Halides: Orthogonal Functionalization of Alkyl Iodides, Bromides, and Chlorides

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 131, Issue 34, Pages 12078-+

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja906040t

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Funding

  1. EPFL

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Ni-catalyzed Sonogashira coupling of nonactivated, B-H-containing alkyl halides, including chlorides, is reported. The coupling is tolerant to a wide range of functional groups, including ether, ester, amide, nitrite, keto, heterocycle, acetal, and aryl halide, in both coupling partners. The coupling can be selective for a specific C-X bond (X = 1, Br, Cl) and allows for orthogonal functionalization of alkyl halides with multiple reactive sites.

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