Issue 44, 2009

Lewis base-catalyzed three-component Strecker reaction on water. An efficient manifold for the direct α-cyanoamination of ketones and aldehydes

Abstract

The first three-component organocatalyzed Strecker reaction operating on water has been developed. The manifold utilizes ketones (aldehydes) as the starting carbonyl component, aniline as the primary amine, acetyl cyanide as the cyanide source and N,N-dimethylcyclohexylamine as the catalyst.

Graphical abstract: Lewis base-catalyzed three-component Strecker reaction on water. An efficient manifold for the direct α-cyanoamination of ketones and aldehydes

Supplementary files

Article information

Article type
Communication
Submitted
22 Jul 2009
Accepted
14 Sep 2009
First published
29 Sep 2009

Chem. Commun., 2009, 6839-6841

Lewis base-catalyzed three-component Strecker reaction on water. An efficient manifold for the direct α-cyanoamination of ketones and aldehydes

F. Cruz-Acosta, A. Santos-Expósito, P. de Armas and F. García-Tellado, Chem. Commun., 2009, 6839 DOI: 10.1039/B914151K

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