Issue 44, 2017

Chemoselective N-arylation of aminobenzamides via copper catalysed Chan–Evans–Lam reactions

Abstract

Chemoselective N-arylation of unprotected aminobenzamides was achieved via Cu-catalysed Chan–Evans–Lam cross-coupling with aryl boronic acids for the first time. Simple copper catalysts enable the selective arylation of amino groups in ortho/meta/para-aminobenzamides under open-flask conditions. The reactions were scalable and compatible with a wide range of functional groups.

Graphical abstract: Chemoselective N-arylation of aminobenzamides via copper catalysed Chan–Evans–Lam reactions

Supplementary files

Article information

Article type
Communication
Submitted
08 Oct 2017
Accepted
23 Oct 2017
First published
23 Oct 2017

Org. Biomol. Chem., 2017,15, 9288-9292

Chemoselective N-arylation of aminobenzamides via copper catalysed Chan–Evans–Lam reactions

S. Liu, W. Zu, J. Zhang and L. Xu, Org. Biomol. Chem., 2017, 15, 9288 DOI: 10.1039/C7OB02491F

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