Issue 42, 2005

Enantioselective conjugate addition of phenylboronic acid to enones catalysed by a chiral tropos/atropos rhodium complex at the coalescence temperature

Abstract

A highly enantioselective rhodium-catalysed conjugate addition of phenylboronic acid to cyclic enones has been achieved using a dynamic library of chiral phosphorus ligands; the tropos/atropos nature of the ligands in the rhodium complex has been characterised via31P-NMR.

Graphical abstract: Enantioselective conjugate addition of phenylboronic acid to enones catalysed by a chiral tropos/atropos rhodium complex at the coalescence temperature

Supplementary files

Article information

Article type
Communication
Submitted
22 Jun 2005
Accepted
31 Aug 2005
First published
21 Sep 2005

Chem. Commun., 2005, 5281-5283

Enantioselective conjugate addition of phenylboronic acid to enones catalysed by a chiral tropos/atropos rhodium complex at the coalescence temperature

C. Monti, C. Gennari and U. Piarulli, Chem. Commun., 2005, 5281 DOI: 10.1039/B508832A

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