Mechanistic Insights into Nickamine-catalyzed Alkyl-Alkyl Cross-coupling Reactions

Authors

  • Jan Breitenfeld Ecole Polytechnique Fédérale de Lausanne Institute of Chemical Sciences and Engineering EPFL-ISIC-LSCI CH-1015 Lausanne, Switzerland
  • Xile Hu Ecole Polytechnique Fédérale de Lausanne Institute of Chemical Sciences and Engineering EPFL-ISIC-LSCI CH-1015 Lausanne, Switzerland. xile.hu@epfl.ch

DOI:

https://doi.org/10.2533/chimia.2014.235

Keywords:

Bimetallic oxidative addition, Cross-coupling, β-hydride elimination, Mechanistic studies, Nickel

Abstract

Within the last decades the transition metal-catalyzed cross-coupling of non-activated alkyl halides has significantly progressed. Within the context of alkyl-alkyl cross-coupling, first row transition metals spanning from iron, over cobalt, nickel, to copper have been successfully applied to catalyze this difficult reaction. The mechanistic understanding of these reactions is still in its infancy. Herein we outline our latest mechanistic studies that explain the efficiency of nickel, in particular nickamine-catalyzed alkyl-alkyl cross-coupling reactions.

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Published

2014-04-30

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