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Formal total synthesis of (±)-conduramine E utilising the Bryce-Smith-Gilbert photoamination reaction

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Chappell, D., Drew, M. G. B. , Gibson, S., Harwood, L. M. and Russell, A. T. (2010) Formal total synthesis of (±)-conduramine E utilising the Bryce-Smith-Gilbert photoamination reaction. Synlett (4). pp. 517-520. ISSN 1437-2096

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To link to this article DOI: 10.1055/s-0029-1219526

Abstract/Summary

Utilising a Bryce-Smith-Gilbert photoamination of benzene as a key step, a synthesis of ()-conduramine E was carried out. A highly regioselective dihydroxylation of a cyclic diene was effected utilising Sharpless AD-mix-b.

Item Type:Article
Refereed:Yes
Divisions:Faculty of Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
Interdisciplinary centres and themes > Chemical Analysis Facility (CAF)
ID Code:9415
Uncontrolled Keywords:Bryce-Smith-Gilbert photoamination - (±)-condur­amine E - diastereocontrolled synthesis
Publisher:Thieme Publishing

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