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Highly enantioselective Michael addition reactions of 2-substituted benzofuran-3(2H)-ones to nitroolefins†
Organic & Biomolecular Chemistry Pub Date : 09/02/2015 00:00:00 , DOI:10.1039/C5OB01691F
Abstract

A highly enantioselective Michael addition reaction of 2-substituted benzofuran-3(2H)-ones to nitroolefins was promoted by a bifunctional squaramide catalyst. As a result, a number of chiral 2,2′-substituted benzofuran-3-one derivatives, bearing adjacent quaternary–tertiary stereocenters, were efficiently synthesized with excellent enantioselectivities.

Graphical abstract: Highly enantioselective Michael addition reactions of 2-substituted benzofuran-3(2H)-ones to nitroolefins
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