Issue 59, 2014

Copper-catalyzed Hiyama cross-coupling using vinylsilanes and benzylic electrophiles

Abstract

Allylbenzene derivatives are ubiquitous frameworks in organic chemistry. Herein is described an efficient copper-catalyzed cross-coupling reaction using vinylsilanes and benzyl bromides, leading to the synthesis of allylbenzenes. This methodology allows the use of cis, trans and 1,1′-disubstituted vinylsilanes as well as a large number of sensitive moieties.

Graphical abstract: Copper-catalyzed Hiyama cross-coupling using vinylsilanes and benzylic electrophiles

Supplementary files

Article information

Article type
Communication
Submitted
20 Apr 2014
Accepted
03 Jun 2014
First published
04 Jun 2014

Chem. Commun., 2014,50, 8018-8020

Author version available

Copper-catalyzed Hiyama cross-coupling using vinylsilanes and benzylic electrophiles

L. Cornelissen, V. Cirriez, S. Vercruysse and O. Riant, Chem. Commun., 2014, 50, 8018 DOI: 10.1039/C4CC02923B

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