Issue 19, 2013

Nickel-catalyzed reductive allylation of aryl bromides with allylic acetates

Abstract

This paper highlights Ni-catalyzed allylation of electron-rich aryl bromides with a variety of substituted allylic carbonates using zinc as the terminal reductant, affording E-alkenes regioselectively in good to excellent yields by the addition of aryl to the less hindered allylic carbon. The electron-deficient aryl bromides and chlorides are also highly efficient coupling partners.

Graphical abstract: Nickel-catalyzed reductive allylation of aryl bromides with allylic acetates

Supplementary files

Article information

Article type
Communication
Submitted
01 Feb 2013
Accepted
02 Apr 2013
First published
02 Apr 2013

Org. Biomol. Chem., 2013,11, 3094-3097

Nickel-catalyzed reductive allylation of aryl bromides with allylic acetates

X. Cui, S. Wang, Y. Zhang, W. Deng, Q. Qian and H. Gong, Org. Biomol. Chem., 2013, 11, 3094 DOI: 10.1039/C3OB40232K

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