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Issue 35, 2012
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Palladium-catalyzed deamidative arylation of azoles with arylamides through a tandem decarbonylation–C–H functionalization

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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

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Article information


Submitted
30 Dec 2011
Accepted
27 Feb 2012
First published
29 Feb 2012

Chem. Commun., 2012,48, 4214-4216
Article type
Communication

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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