Issue 3, 2016

Attractive aerobic access to the α,β-unsaturated acyl azolium intermediate: oxidative NHC catalysis via multistep electron transfer

Abstract

To replace high molecular weight oxidants with air (O2) we introduce multistep electron transfer NHC catalysis. The method provides a general and selective oxidation of the α,β-unsaturated aldehyde derived homoenolate to the synthetically useful α,β-unsaturated acyl azolium intermediate. Several independent oxidative NHC-catalyzed reactions are viable with this strategy and the products can be isolated in high to excellent yields.

Graphical abstract: Attractive aerobic access to the α,β-unsaturated acyl azolium intermediate: oxidative NHC catalysis via multistep electron transfer

Supplementary files

Article information

Article type
Communication
Submitted
21 Aug 2015
Accepted
21 Sep 2015
First published
30 Sep 2015
This article is Open Access
Creative Commons BY license

Green Chem., 2016,18, 686-690

Author version available

Attractive aerobic access to the α,β-unsaturated acyl azolium intermediate: oxidative NHC catalysis via multistep electron transfer

L. Ta, A. Axelsson and H. Sundén, Green Chem., 2016, 18, 686 DOI: 10.1039/C5GC01965F

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