Issue 31, 2010

Cyclopropenium ion catalysed Beckmann rearrangement

Abstract

1-Chloro-2,3-diphenylcyclopropenium ion was found to be a very efficient organocatalyst (3 mol% loading) for liquid phase Beckmann rearrangement of various ketoximes to the corresponding amides/lactams within 2 h in acetonitrile at reflux temperature. This is the first example of the application of the cyclopropenium ion as a catalyst, which opens up a new aspect of the synthetic utility of aromatic cation based catalysis.

Graphical abstract: Cyclopropenium ion catalysed Beckmann rearrangement

Supplementary files

Article information

Article type
Communication
Submitted
07 Apr 2010
Accepted
08 Jun 2010
First published
01 Jul 2010

Chem. Commun., 2010,46, 5808-5810

Cyclopropenium ion catalysed Beckmann rearrangement

V. P. Srivastava, R. Patel, Garima and L. D. S. Yadav, Chem. Commun., 2010, 46, 5808 DOI: 10.1039/C0CC00815J

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