Issue 18, 2019

Ni-Catalyzed enantioselective reductive aryl-alkenylation of alkenes: application to the synthesis of (+)-physovenine and (+)-physostigmine

Abstract

A Ni-catalyzed enantioselective reductive aryl-alkenylation of alkenes by cyclizative coupling of an aryl bromide and a vinyl bromide is developed, providing efficient access to functionalized 3,3-disubstituted oxindoles under mild conditions, without requiring the use of preformed vinylmetallic reagents. With this method, a concise formal synthesis of (+)-physovenine and (+)-physostigmine has been completed.

Graphical abstract: Ni-Catalyzed enantioselective reductive aryl-alkenylation of alkenes: application to the synthesis of (+)-physovenine and (+)-physostigmine

Supplementary files

Article information

Article type
Research Article
Submitted
08 Jun 2019
Accepted
09 Aug 2019
First published
16 Aug 2019

Org. Chem. Front., 2019,6, 3305-3309

Ni-Catalyzed enantioselective reductive aryl-alkenylation of alkenes: application to the synthesis of (+)-physovenine and (+)-physostigmine

Y. Li, Z. Ding, A. Lei and W. Kong, Org. Chem. Front., 2019, 6, 3305 DOI: 10.1039/C9QO00744J

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