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Murray, Adrian J and Parsons, Philip J (2006) A convenient approach to (-)-8-epi-swainsonine. Synlett, - (9). pp. 1443-1445. ISSN 09365214
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Official URL: http://dx.doi.org/10.1055/s-2006-939710
Abstract
A novel and efficient synthesis of (-)-8-epi-swainsonine (2) is reported. Face-selective diol formation from the bicyclic alkene 3 followed by a stereoselective vinylation of the aldehyde and ring-closing metathesis gave the indolizidine ring system, which was converted into (-)-8-epi-swainsonine (2).
Item Type: | Article |
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Schools and Departments: | School of Life Sciences > Chemistry |
Depositing User: | Philip Parsons |
Date Deposited: | 06 Feb 2012 19:03 |
Last Modified: | 21 Mar 2012 09:37 |
URI: | http://sro.sussex.ac.uk/id/eprint/19158 |