Clark, J.S. , Baxter, C. A. and Castro, J. L. (2005) Synthesis of the tricyclic core of the marine natural product labiatin A. Synthesis(19), pp. 3398-3404. (doi: 10.1055/s-2005-918485)
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Publisher's URL: http://dx.doi.org/10.1055/s-2005-918485
Abstract
A synthetic route to a model of the tricyclic core of labiatin A is described. Two catalytic metal carbenoid reactions, C-H insertion and oxonium ylide generation with subsequent [2,3]-sigmatropic rearrangement, have been used to assemble the tricyclic system in an efficient and stereoselective manner.
Item Type: | Articles |
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Status: | Published |
Refereed: | Yes |
Glasgow Author(s) Enlighten ID: | Clark, Professor Stephen |
Authors: | Clark, J.S., Baxter, C. A., and Castro, J. L. |
College/School: | College of Science and Engineering > School of Chemistry |
Journal Name: | Synthesis |
Publisher: | Georg Thieme Verlag |
ISSN: | 0039-7881 |
ISSN (Online): | 1437-210X |
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