Issue 17, 2003
From the journal:

Organic & Biomolecular Chemistry

Studies on the intramolecular Kulinkovich–de Meijere reaction of disubstituted alkenes bearing carboxylic amide groups

Nouara Ouhamoua  and  Yvan Six*a  

* Corresponding authors

a Institut de Chimie des Substances Naturelles, U.P.R. 2301 du C.N.R.S., Avenue de la Terrasse, 91198 Gif-sur-Yvette, France
E-mail: Yvan.Six@icsn.cnrs-gif.fr
Fax: 33 (1) 69 07 72 47
Tel: 33 (1) 69 82 30 83

Abstract

1,2-Disubstituted olefins bearing an acetamide group were found to undergo intramolecular Kulinkovich–de Meijere cyclopropanation in moderate yield but almost complete diastereoselectivity.

Graphical abstract: Studies on the intramolecular Kulinkovich–de Meijere reaction of disubstituted alkenes bearing carboxylic amide groups

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Article information

DOI
https://doi.org/10.1039/B306719J
Article type
Communication
Submitted
16 Jun 2003
Accepted
31 Jul 2003
First published
05 Aug 2003

Org. Biomol. Chem., 2003,1, 3007-3009

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Studies on the intramolecular Kulinkovich–de Meijere reaction of disubstituted alkenes bearing carboxylic amide groups

N. Ouhamou and Y. Six, Org. Biomol. Chem., 2003, 1, 3007 DOI: 10.1039/B306719J

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