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  4. Ni-Catalyzed Sonogashira Coupling of Non-activated Alkyl Halides: Orthogonal Functionalization of Alkyl Iodides, Bromides, and Chlorides
 
research article

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

Vechorkin, Oleg  
•
Barmaz, Delphine
•
Proust, Valérie
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2009
Journal of the American Chemical Society

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

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Type
research article
DOI
10.1021/ja906040t
Web of Science ID

WOS:000269379600029

Author(s)
Vechorkin, Oleg  
Barmaz, Delphine
Proust, Valérie
Hu, Xile  
Date Issued

2009

Published in
Journal of the American Chemical Society
Volume

131

Issue

34

Start page

12078

End page

12079

Subjects

Grignard-Reagents

•

Nickel-Complexes

•

Cross-Couplings

•

Acetylides

•

Ligand

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCI  
Available on Infoscience
August 6, 2009
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/41986
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