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


Autoria(s): Chappell, David; Drew, Michael G B; Gibson, Shane; Harwood, Laurence M; Russell, Andrew Timothy
Data(s)

11/02/2010

Resumo

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.

Formato

text

Identificador

http://centaur.reading.ac.uk/9415/1/Conduramine_E_Final.pdf

Chappell, D. <http://centaur.reading.ac.uk/view/creators/90000971.html>, Drew, M. G. B. , Gibson, S., Harwood, L. M. <http://centaur.reading.ac.uk/view/creators/90000170.html> and Russell, A. T. <http://centaur.reading.ac.uk/view/creators/90000368.html> (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 <http://dx.doi.org/10.1055/s-0029-1219526>

Idioma(s)

en

Publicador

Thieme Publishing

Relação

http://centaur.reading.ac.uk/9415/

creatorInternal Chappell, David

creatorInternal Harwood, Laurence M

creatorInternal Russell, Andrew Timothy

10.1055/s-0029-1219526

Tipo

Article

PeerReviewed