Issue 20, 2013

Phosphine-catalyzed [3+2] annulation of α-substituted allenoates with ester-activated α,β-unsaturated imines: a novel variation of the Lu [3+2] cycloaddition reaction

Abstract

A phosphine-catalyzed [3+2] annulation reaction of α-substituted allenoates with ester-activated α,β-unsaturated imines is reported, which provides new and efficient access to highly functionalized cyclopentenes bearing one all-carbon quaternary center. This reaction also expands the scope of the famous Lu [3+2] cycloaddition reaction.

Graphical abstract: Phosphine-catalyzed [3+2] annulation of α-substituted allenoates with ester-activated α,β-unsaturated imines: a novel variation of the Lu [3+2] cycloaddition reaction

Supplementary files

Article information

Article type
Communication
Submitted
16 Nov 2012
Accepted
14 Jan 2013
First published
17 Jan 2013

Chem. Commun., 2013,49, 2058-2060

Phosphine-catalyzed [3+2] annulation of α-substituted allenoates with ester-activated α,β-unsaturated imines: a novel variation of the Lu [3+2] cycloaddition reaction

J. Tian and Z. He, Chem. Commun., 2013, 49, 2058 DOI: 10.1039/C3CC38264H

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