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Enantioselective synthesis of pyrazolone derivatives catalysed by a chiral squaramide catalyst

RSC AdvancesPublished 1 January 2014
Junhua Li, Da‐Ming Du
Citations21
SJR quartileQ1
SJR score0.78
SNIP0.96

TL;DR

An efficient chiral squaramide-catalysed enantioselective Michael addition of pyrazolin-5-ones to β,γ-unsaturated α-ketoesters has been developed and provides valuable and easy access to chiral pyrazolone ketoester derivatives.

Abstract

An efficient chiral squaramide-catalysed enantioselective Michael addition of pyrazolin-5-ones to β,γ-unsaturated α-ketoesters has been developed. The chiral pyrazolone derivatives were obtained in moderate to high yields (up to 99% yield) with high enantioselectivities (up to 96% ee) for most substrates. This catalytic asymmetric reaction provides valuable and easy access to chiral pyrazolone ketoester derivatives.

Keywords

ChemistryBiochemistry, Genetics and Molecular Biology