Issue 20, 2015

Enantioselective synthesis of chiral heterocycles containing both chroman and pyrazolone derivatives catalysed by a chiral squaramide

Abstract

An efficient chiral squaramide-catalysed enantioselective Michael addition of pyrazolin-5-ones to 3-nitro-2H-chromenes for the synthesis of chiral heterocyclic systems containing both chroman and pyrazolone derivatives has been developed. This reaction afforded the desired products in high to excellent yields (up to 98%) with high enantioselectivities (up to 96%) and excellent diastereoselectivities (up to 99 : 1) under very low catalyst loading (0.2 mol%). This catalytic asymmetric reaction provides an efficient route toward the synthesis of chiral heterocyclic systems containing both chroman and pyrazolone derivatives, which possess potential pharmaceutical activities.

Graphical abstract: Enantioselective synthesis of chiral heterocycles containing both chroman and pyrazolone derivatives catalysed by a chiral squaramide

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
23 Dec 2014
Accepted
09 Apr 2015
First published
09 Apr 2015

Org. Biomol. Chem., 2015,13, 5636-5645

Author version available

Enantioselective synthesis of chiral heterocycles containing both chroman and pyrazolone derivatives catalysed by a chiral squaramide

J. Li and D. Du, Org. Biomol. Chem., 2015, 13, 5636 DOI: 10.1039/C4OB02653E

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