Issue 73, 2017

Direct, efficient NHC-catalysed aldehyde oxidative amidation: in situ formed benzils as unconventional acylating agents

Abstract

A new N-heterocyclic carbene-catalysed oxidative amidation of aldehydes has been developed which converts the aldehyde to a benzil acylating agent in situ. The process uses an air-recyclable oxidant and a nucleophilic co-catalyst and does not require the use of a large excess of either one coupling partner or catalyst.

Graphical abstract: Direct, efficient NHC-catalysed aldehyde oxidative amidation: in situ formed benzils as unconventional acylating agents

Supplementary files

Article information

Article type
Communication
Submitted
18 Jul 2017
Accepted
24 Aug 2017
First published
01 Sep 2017

Chem. Commun., 2017,53, 10212-10215

Direct, efficient NHC-catalysed aldehyde oxidative amidation: in situ formed benzils as unconventional acylating agents

V. Kumar and S. J. Connon, Chem. Commun., 2017, 53, 10212 DOI: 10.1039/C7CC05561G

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