Issue 76, 2015

An asymmetric allylic alkylation reaction of 3-alkylidene oxindoles

Abstract

An efficient asymmetric allylic alkylation reaction with respect to 3-alkylidene oxindoles and racemic Morita–Baylis–Hillman carbonate has been achieved by using a chiral biscinchona alkaloid catalyst, which delivers the γ-substituted alkylideneoxindoles with a chiral tertiary center in moderate to good yields (up to 92%) and very good enantioselectivities (up to >99% ee).

Graphical abstract: An asymmetric allylic alkylation reaction of 3-alkylidene oxindoles

Supplementary files

Article information

Article type
Communication
Submitted
23 Jul 2015
Accepted
07 Aug 2015
First published
07 Aug 2015

Chem. Commun., 2015,51, 14342-14345

An asymmetric allylic alkylation reaction of 3-alkylidene oxindoles

J. Feng, X. Li and J. Cheng, Chem. Commun., 2015, 51, 14342 DOI: 10.1039/C5CC06182B

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