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Organocatalytic asymmetric Henry reaction of isatins: Highly enantioselective synthesis of 3-hydroxy-2-oxindoles†
Yong Zhang,Zhi Jun Li,Hai Sen Xu,Yuan Zhang,Wei Wang
RSC Advances Pub Date : 08/18/2011 00:00:00 , DOI:10.1039/C1RA00477H
Abstract

Organocatalytic asymmetric Henry reaction of isatins with nitromethane has been achieved with the use of C6′-OH cinchona alkaloid catalyst, affording 3-substituted 3-hydroxy-oxindoles in excellent yields and high enantioselectivities, and this method was successfully applied to the total synthesis of (R)-(+)-dioxibrassinin.

Graphical abstract: Organocatalytic asymmetric Henry reaction of isatins: Highly enantioselective synthesis of 3-hydroxy-2-oxindoles
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