Issue 28, 2015

Rhenium-catalyzed C–H aminocarbonylation of azobenzenes with isocyanates

Abstract

The first C–H aminocarbonylation of azobenzenes with isocyanates is achieved by using rhenium-catalysis, which provides an expedient and atom-economical access to varied o-azobenzamides from readily available starting materials. The reaction efficiency can be enhanced by the catalytic use of sodium acetate via accelerated C–H bond activation.

Graphical abstract: Rhenium-catalyzed C–H aminocarbonylation of azobenzenes with isocyanates

Supplementary files

Article information

Article type
Communication
Submitted
04 Jun 2015
Accepted
05 Jun 2015
First published
09 Jun 2015

Org. Biomol. Chem., 2015,13, 7619-7623

Rhenium-catalyzed C–H aminocarbonylation of azobenzenes with isocyanates

X. Geng and C. Wang, Org. Biomol. Chem., 2015, 13, 7619 DOI: 10.1039/C5OB01121C

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