Issue 8, 2016

Copper-catalyzed decarboxylative cross-coupling of cinnamic acids and ACCN via single electron transfer

Abstract

A novel and convenient method for the synthesis of β,γ-unsaturated nitriles using ACCN (1,1′-azobis(cyclohexane-1-carbonitrile)) as a cyano source was described. This reaction was amenable to a broad range of substrates and provided the desired β,γ-unsaturated nitriles containing an all-carbon quaternary carbon center in moderate yields with high selectivity via single electron transfer and decarboxylation.

Graphical abstract: Copper-catalyzed decarboxylative cross-coupling of cinnamic acids and ACCN via single electron transfer

Supplementary files

Article information

Article type
Communication
Submitted
30 Dec 2015
Accepted
27 Jan 2016
First published
27 Jan 2016

Org. Biomol. Chem., 2016,14, 2399-2402

Copper-catalyzed decarboxylative cross-coupling of cinnamic acids and ACCN via single electron transfer

B. Gao, Y. Xie, L. Yang and H. Huang, Org. Biomol. Chem., 2016, 14, 2399 DOI: 10.1039/C5OB02677F

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