Issue 8, 2019

Asymmetric organocatalytic conjugated addition of pyrazolin-5-ones to ortho-quinomethanes: construction of vicinal tertiary and all-carbon quaternary stereocenters

Abstract

A chiral amine squaramide catalyzed the conjugated addition of pyrazolin-5-ones to in situ generated ortho-quinomethanes (o-QMs) was developed to construct 4-tetrasubstituted pyrazolin-5-ones featuring adjacent quaternary and tertiary stereocenters in oil–water phases. High yields, excellent stereoselectivities, mild conditions and accessible scale-up demonstrated the fascination of this reaction protocol.

Graphical abstract: Asymmetric organocatalytic conjugated addition of pyrazolin-5-ones to ortho-quinomethanes: construction of vicinal tertiary and all-carbon quaternary stereocenters

Supplementary files

Article information

Article type
Research Article
Submitted
04 Jan 2019
Accepted
26 Feb 2019
First published
27 Feb 2019

Org. Chem. Front., 2019,6, 1140-1145

Asymmetric organocatalytic conjugated addition of pyrazolin-5-ones to ortho-quinomethanes: construction of vicinal tertiary and all-carbon quaternary stereocenters

M. Chu, S. Qi, W. Ju, Y. Wang, X. Chen, D. Xu and Z. Xu, Org. Chem. Front., 2019, 6, 1140 DOI: 10.1039/C9QO00011A

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