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  4. Suzuki-Miyaura Cross-Coupling Reactions of Unactivated Alkyl Halides Catalyzed by a Nickel Pincer Complex
 
research article

Suzuki-Miyaura Cross-Coupling Reactions of Unactivated Alkyl Halides Catalyzed by a Nickel Pincer Complex

Di Franco, Thomas  
•
Boutin, Nicolas
•
Hu, Xile  
2013
Synthesis: Journal of Synthetic Organic Chemistry

A nickel(II) pincer complex, [((N2N)-N-Me)Ni-Cl], was used to catalyze alkyl-alkyl and alkyl-aryl Suzuki-Miyaura coupling reactions of unactivated alkyl halides. The coupling of 9-alkyl-9-borabicyclo[3.3.1]nonane and 9-phenyl-9-borabicyclo[3.3.1]nonane reagents with alkyl halides was achieved in modest to good yields. The reactions tolerated a variety of useful functional groups including ester, ether, furan, thioether, acetal, and Boc groups.

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Type
research article
DOI
10.1055/s-0033-1338544
Web of Science ID

WOS:000325931800004

Author(s)
Di Franco, Thomas  
Boutin, Nicolas
Hu, Xile  
Date Issued

2013

Publisher

Georg Thieme Verlag

Published in
Synthesis: Journal of Synthetic Organic Chemistry
Volume

45

Issue

21

Start page

2949

End page

2958

Subjects

cross coupling

•

nickel

•

alkyl halides

•

pincer complex

•

Suzuki-Miyaura coupling

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCI  
Available on Infoscience
December 9, 2013
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/97642
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