Issue 3, 2011

Chemoselective phosphine-catalyzed cascade annulations between two different activated alkenes: highly diastereoselective syntheses of polysubstituted cyclohexanes and cyclopentenes

Abstract

Chemoselective phosphine-catalyzed cascade [2 + 2 + 2] and [2 + 2 + 1] annulations between two molecules of 2-arylmethylidene cyanoacetates or malononitriles and one molecule of α,β-unsaturated ketones have been developed. Under the nucleophilic catalysis of PPh3 or PBu3 (10 mol%), a highly diastereoselective synthesis of polysubstituted cyclohexanes or cyclopentenes has been successfully achieved, respectively.

Graphical abstract: Chemoselective phosphine-catalyzed cascade annulations between two different activated alkenes: highly diastereoselective syntheses of polysubstituted cyclohexanes and cyclopentenes

Supplementary files

Article information

Article type
Communication
Submitted
26 Jul 2010
Accepted
15 Oct 2010
First published
15 Nov 2010

Chem. Commun., 2011,47, 1045-1047

Chemoselective phosphine-catalyzed cascade annulations between two different activated alkenes: highly diastereoselective syntheses of polysubstituted cyclohexanes and cyclopentenes

L. Cai, B. Zhang, G. Wu, H. Song and Z. He, Chem. Commun., 2011, 47, 1045 DOI: 10.1039/C0CC02817G

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