Issue 22, 2014

Catalytic, enantioselective vinylogous Michael reactions

Abstract

Recent progress in the field of catalytic, enantioselective vinylogous Michael reactions of latent dienolates is described which furnish optically highly enriched chiral 1,7-dioxo compounds of great utility in one synthetic operation. Emphasis is given to new catalysis modes which realise this challenging transformation with high regio- as well as enantioselectivity.

Graphical abstract: Catalytic, enantioselective vinylogous Michael reactions

Article information

Article type
Review Article
Submitted
13 Feb 2014
Accepted
25 Mar 2014
First published
25 Mar 2014

Org. Biomol. Chem., 2014,12, 3531-3543

Catalytic, enantioselective vinylogous Michael reactions

C. Schneider and F. Abels, Org. Biomol. Chem., 2014, 12, 3531 DOI: 10.1039/C4OB00332B

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