Issue 52, 2014

Organocatalytic direct asymmetric vinylogous Mannich reaction of γ-butenolides with isatin-derived ketimines

Abstract

The first direct asymmetric vinylogous Mannich reaction of γ-butenolides with isatin-derived ketimines has been effectively realized promoted by a bifunctional quinidine-derived catalyst. A series of chiral 3-aminooxindole derivatives bearing adjacent tertiary and quaternary stereocenters with the butenolide moiety were obtained in excellent yields (up to 97%) and high enantioselectivities (up to 96% ee).

Graphical abstract: Organocatalytic direct asymmetric vinylogous Mannich reaction of γ-butenolides with isatin-derived ketimines

Supplementary files

Article information

Article type
Communication
Submitted
22 May 2014
Accepted
10 Jun 2014
First published
11 Jun 2014

RSC Adv., 2014,4, 27286-27289

Organocatalytic direct asymmetric vinylogous Mannich reaction of γ-butenolides with isatin-derived ketimines

Y. Guo, Y. Zhang, L. Qi, F. Tian and L. Wang, RSC Adv., 2014, 4, 27286 DOI: 10.1039/C4RA04824E

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