Accessibility navigation


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

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

[img] Text - Accepted Version
· Please see our End User Agreement before downloading.

518kB

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

To link to this item 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

Downloads

Downloads per month over past year

University Staff: Request a correction | Centaur Editors: Update this record

Page navigation