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Asymmetric Mannich reaction: highly enantioselective synthesis of 3-amino-oxindoles via chiral squaramide based H-bond donor catalysis†
Kadiyala Srinivasa Rao,Pambala Ramesh,L. Raju Chowhan,Rajiv Trivedi
RSC Advances Pub Date : 08/31/2016 00:00:00 , DOI:10.1039/C6RA16877A
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
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