Issue 35, 2012

Palladium-catalyzed deamidative arylation of azoles with arylamides through a tandem decarbonylation–C–H functionalization

Abstract

A highly chemo-, regio-selective, and efficient palladium-catalyzed deamidative arylation of azoles with arylamides, as an aryl metal equivalent, has been developed. The reaction proceeds smoothly to generate the corresponding products in good yields via a tandem decarbonylation–C–H activation.

Graphical abstract: Palladium-catalyzed deamidative arylation of azoles with arylamides through a tandem decarbonylation–C–H functionalization

Supplementary files

Article information

Article type
Communication
Submitted
30 Dec 2011
Accepted
27 Feb 2012
First published
29 Feb 2012

Chem. Commun., 2012,48, 4214-4216

Palladium-catalyzed deamidative arylation of azoles with arylamides through a tandem decarbonylation–C–H functionalization

C. Li, P. Li, J. Yang and L. Wang, Chem. Commun., 2012, 48, 4214 DOI: 10.1039/C2CC18156H

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