Issue 9, 2013

An organocatalytic asymmetric double Michael cascade reaction of unsaturated ketones and unsaturated pyrazolones: highly efficient synthesis of spiropyrazolone derivatives

Abstract

The first organocatalytic double Michael cascade reaction between unsaturated ketones and unsaturated pyrazolones has been developed which provides spiropyrazolone core structures containing two interval or three consecutive stereogenic centers with excellent diastereo- (>20 : 1) and enantioselectivities (up to 99% ee). Moreover, a pair of enantiomers 5 and 5′ can be achieved via different catalysts.

Graphical abstract: An organocatalytic asymmetric double Michael cascade reaction of unsaturated ketones and unsaturated pyrazolones: highly efficient synthesis of spiropyrazolone derivatives

Supplementary files

Article information

Article type
Communication
Submitted
27 Oct 2012
Accepted
10 Dec 2012
First published
11 Dec 2012

Org. Biomol. Chem., 2013,11, 1441-1445

An organocatalytic asymmetric double Michael cascade reaction of unsaturated ketones and unsaturated pyrazolones: highly efficient synthesis of spiropyrazolone derivatives

J. Liang, Q. Chen, L. Liu, X. Jiang and R. Wang, Org. Biomol. Chem., 2013, 11, 1441 DOI: 10.1039/C2OB27095A

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