Issue 7, 2008

Pd-catalysed asymmetric mono- and bis-alkoxycarbonylation of vinylarenes

Abstract

The asymmetric alkoxycarbonylation of vinylarenes catalysed by palladium complexes bearing chiral phosphine ligands has attracted much attention over the last decades. The products of both mono- and bis(alkoxycarbonylation) reactions are important intermediates in the syntheses of pharmaceuticals such as 2-arylpropionic acids, the most important class of non-steroidal anti-inflammatory drugs. In this article, a general overview of the topics will be presented and the recent advances in this field will be particularly detailed. Besides the term alkoxycarbonylation, hydroesterification and hydroalkoxycarbonylation are also used in the literature to describe this reaction. Furthermore, more specific terms such as methoxycarbonylation can be found. In this report, the term alkoxycarbonylation will be used as the general term, and specific terms will be used to unambiguously define which reaction is meant.

Graphical abstract: Pd-catalysed asymmetric mono- and bis-alkoxycarbonylation of vinylarenes

Article information

Article type
Perspective
Submitted
26 Sep 2007
Accepted
14 Nov 2007
First published
10 Dec 2007

Dalton Trans., 2008, 853-860

Pd-catalysed asymmetric mono- and bis-alkoxycarbonylation of vinylarenes

C. Godard, B. K. Muñoz, A. Ruiz and C. Claver, Dalton Trans., 2008, 853 DOI: 10.1039/B714809G

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