Formal total synthesis of (±)-conduramine E utilising the Bryce-Smith-Gilbert photoamination reaction
Data(s) |
11/02/2010
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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 |