Issue 4, 2011

Metallacycle-mediated cross-coupling with substituted and electronically unactivated alkenes

Abstract

This perspective surveys the history of – and recent advances in – metallacycle-mediated coupling chemistry of substituted alkenes. While the reaction of preformed metal–π complexes with ethylene was reported nearly 30 years ago, the generalization of this mode of bimolecular C–C bond formation to the regio- and stereoselective union of complex substrates has only recently begun to emerge. This perspective discusses early observations in this area, the challenges associated with controlling such processes, the evolution of a general strategy to overcome these challenges, and a summary of highly regio- and stereoselective convergent coupling reactions that are currently available via metallacycle-mediated cross-coupling of substituted alkenes.

Graphical abstract: Metallacycle-mediated cross-coupling with substituted and electronically unactivated alkenes

Article information

Article type
Perspective
Submitted
27 Jul 2010
Accepted
13 Oct 2010
First published
15 Nov 2010

Chem. Sci., 2011,2, 573-589

Metallacycle-mediated cross-coupling with substituted and electronically unactivated alkenes

H. A. Reichard and G. C. Micalizio, Chem. Sci., 2011, 2, 573 DOI: 10.1039/C0SC00394H

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