Issue 87, 2016

Asymmetric Mannich reaction: highly enantioselective synthesis of 3-amino-oxindoles via chiral squaramide based H-bond donor catalysis

Abstract

We describe here a simple and facile asymmetric Mannich reaction catalyzed by chiral Cinchona alkaloid based squaramide containing H-bond donor catalysts, wherein, the reaction of 1,3-diketones with isatin (N-Boc) ketimines led to the formation of 3-aminooxindole derivatives. These derivatives were obtained in high yields with excellent enantioselectivities under mild conditions using 3 mol% of the catalyst. This protocol provides valuable and easy access to chiral 3-substituted 3-aminooxindole derivatives.

Graphical abstract: Asymmetric Mannich reaction: highly enantioselective synthesis of 3-amino-oxindoles via chiral squaramide based H-bond donor catalysis

Supplementary files

Article information

Article type
Communication
Submitted
30 Jun 2016
Accepted
31 Aug 2016
First published
31 Aug 2016

RSC Adv., 2016,6, 84242-84247

Asymmetric Mannich reaction: highly enantioselective synthesis of 3-amino-oxindoles via chiral squaramide based H-bond donor catalysis

K. S. Rao, P. Ramesh, L. R. Chowhan and R. Trivedi, RSC Adv., 2016, 6, 84242 DOI: 10.1039/C6RA16877A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements