Issue 78, 2016

Direct NHC-catalysed redox amidation using CO2 for traceless masking of amine nucleophiles

Abstract

The N-heterocyclic carbene (NHC)-catalysed redox amidation reaction is poorly developed and usually requires catalytic co-additives for electron-rich amine nucleophiles. We report a masking strategy (using CO2) that couples release of the free amine nucleophile to catalytic turnover, and in doing so, enables direct catalytic redox amidation of electron-rich amines.

Graphical abstract: Direct NHC-catalysed redox amidation using CO2 for traceless masking of amine nucleophiles

Supplementary files

Article information

Article type
Communication
Submitted
02 Jun 2016
Accepted
28 Jul 2016
First published
28 Jul 2016
This article is Open Access
Creative Commons BY license

Chem. Commun., 2016,52, 11638-11641

Author version available

Direct NHC-catalysed redox amidation using CO2 for traceless masking of amine nucleophiles

R. W. M. Davidson and M. J. Fuchter, Chem. Commun., 2016, 52, 11638 DOI: 10.1039/C6CC04639H

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