Issue 6, 2008

Ruthenium-catalyzed tandem allylic substitution/isomerization: a direct route to propiophenones from cinnamyl chloride derivatives

Abstract

A tandem nucleophilicsubstitution/redox isomerization catalyzed by a single ruthenium catalyst leads to the direct transformation of allylic chlorides into propiophenones.

Graphical abstract: Ruthenium-catalyzed tandem allylic substitution/isomerization: a direct route to propiophenones from cinnamyl chloride derivatives

Article information

Article type
Letter
Submitted
22 Jan 2008
Accepted
28 Mar 2008
First published
15 Apr 2008

New J. Chem., 2008,32, 929-931

Ruthenium-catalyzed tandem allylic substitution/isomerization: a direct route to propiophenones from cinnamyl chloride derivatives

M. Helou, J. Renaud, B. Demerseman, F. Carreaux and C. Bruneau, New J. Chem., 2008, 32, 929 DOI: 10.1039/B801159A

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