Issue 45, 2013

Chiral olefin–sulfoxide as ligands for rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to unsaturated esters

Abstract

An efficient rhodium/olefin–sulfoxide catalyzed asymmetric conjugate addition of organoboronic acids to various unsaturated esters has been developed, where 2-methoxy-1-naphthyl sulfinyl functionalized olefin ligands have been shown to be highly effective, and are especially applicable to unsaturated methyl esters with up to 99% yield and 91% ee.

Graphical abstract: Chiral olefin–sulfoxide as ligands for rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to unsaturated esters

Supplementary files

Article information

Article type
Paper
Submitted
01 Jul 2013
Accepted
26 Sep 2013
First published
27 Sep 2013

Org. Biomol. Chem., 2013,11, 7893-7898

Chiral olefin–sulfoxide as ligands for rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to unsaturated esters

F. Xue, D. Wang, X. Li and B. Wan, Org. Biomol. Chem., 2013, 11, 7893 DOI: 10.1039/C3OB41342J

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