Issue 6, 2016

Palladium-catalyzed C–H bond carboxylation of acetanilides: an efficient usage of N,N-dimethyloxamic acid as the carboxylate source

Abstract

N,N-Dimethyloxamic acid can be successfully employed as a carboxylate precursor in the palladium-catalyzed direct C–H carboxylation of acetanilides. The reaction proceeds smoothly under mild conditions over a broad range of substrates with high functional group tolerance, affording substituted N-acyl anthranilic acids in moderate to high yields.

Graphical abstract: Palladium-catalyzed C–H bond carboxylation of acetanilides: an efficient usage of N,N-dimethyloxamic acid as the carboxylate source

Supplementary files

Article information

Article type
Communication
Submitted
20 Sep 2015
Accepted
17 Nov 2015
First published
17 Nov 2015

Chem. Commun., 2016,52, 1286-1289

Author version available

Palladium-catalyzed C–H bond carboxylation of acetanilides: an efficient usage of N,N-dimethyloxamic acid as the carboxylate source

Y. Wu, C. Jiang, D. Wu, Q. Gu, Z. Luo and H. Luo, Chem. Commun., 2016, 52, 1286 DOI: 10.1039/C5CC07890C

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