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

Chappell, D., Drew, M. G. B., Gibson, S., Harwood, L. M. ORCID: https://orcid.org/0000-0002-8442-7380 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 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
URI	https://reading-clone.eprints-hosting.org/id/eprint/9415
Identification Number/DOI	10.1055/s-0029-1219526
Refereed	Yes
Divisions	Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry Interdisciplinary centres and themes > Chemical Analysis Facility (CAF)
Uncontrolled Keywords	Bryce-Smith-Gilbert photoamination - (±)-condur­amine E - diastereocontrolled synthesis
Publisher	Thieme Publishing
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