Issue 42, 2006

Switching stereoselectivity in rhodium-catalysed 1,4-additions: the asymmetric synthesis of 2-substituted pyrrolizidinones

Abstract

The appropriate choice of organometallic nucleophile enables the straightforward preparation of different stereoisomers of 2-substituted pyrrolizidinones utilising the rhodium-catalysed 1,4-addition reaction.

Graphical abstract: Switching stereoselectivity in rhodium-catalysed 1,4-additions: the asymmetric synthesis of 2-substituted pyrrolizidinones

Supplementary files

Article information

Article type
Communication
Submitted
14 Jul 2006
Accepted
18 Sep 2006
First published
03 Oct 2006

Chem. Commun., 2006, 4389-4391

Switching stereoselectivity in rhodium-catalysed 1,4-additions: the asymmetric synthesis of 2-substituted pyrrolizidinones

J. D. Hargrave, G. Bish and C. G. Frost, Chem. Commun., 2006, 4389 DOI: 10.1039/B610128C

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