4.0 Article

A new procedure for the enantioselective vinylogous aldol reaction of Chan's diene

Journal

TETRAHEDRON-ASYMMETRY
Volume 17, Issue 24, Pages 3332-3334

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2006.12.016

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Chiral delta-hydroxy-delta-ketoesters are easily available through the enantio selective vinylogous aldol reaction of Chan's diene promoted by a SiCl4/chiral phosphoramide catalytic system. The procedure is conveniently exploited for a very rapid approach to (+)-kavain, a natural bio-active alpha-pyrone compound. (c) 2007 Elsevier Ltd. All rights reserved.

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