Issue 5, 2020

Organo-catalyzed asymmetric cascade annulation reaction for the construction of bi-spirocyclic pyrazolone and oxindole derivatives

Abstract

A bifunctional organocatalyst catalyzed tandem annulation reaction between β,γ-unsaturated α-ketoesters with α-arylidene pyrazolinones was reported. The tandem Michael–aldol process allows access to optically active bi-spirocyclic pyrazolone and oxindole compounds in high yields with good to excellent enantioselectivity and diastereoselectivity. The resulting bi-spirocyclic compounds possess highly dense functionalized substituents, two all-carbon spiro quaternary stereocenters and one hemiketal stereogenic centers.

Graphical abstract: Organo-catalyzed asymmetric cascade annulation reaction for the construction of bi-spirocyclic pyrazolone and oxindole derivatives

Supplementary files

Article information

Article type
Research Article
Submitted
03 Jan 2020
Accepted
05 Feb 2020
First published
07 Feb 2020

Org. Chem. Front., 2020,7, 796-809

Organo-catalyzed asymmetric cascade annulation reaction for the construction of bi-spirocyclic pyrazolone and oxindole derivatives

B. Sun, J. Chen, J. Zhang, X. Yang, H. Lv, Z. Wang and X. Wang, Org. Chem. Front., 2020, 7, 796 DOI: 10.1039/D0QO00001A

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