Stereoselective synthesis of the cytotoxic macrolide aspergillide B
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Show full item recordcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/8639
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http://dx.doi.org/10.1016/j.tetlet.2009.04.026 |
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Title
Stereoselective synthesis of the cytotoxic macrolide aspergillide BAuthor (s)
Date
2009Publisher
ElsevierISSN
404039Bibliographic citation
Tetrahedron Letters, 50, 27, p. 3783-3785Type
info:eu-repo/semantics/articleSubject
Abstract
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A cross metathesis and a C-glycosidation via a Mukaiyama-type aldol reaction were key features of the synthesis. The ... [+]
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A cross metathesis and a C-glycosidation via a Mukaiyama-type aldol reaction were key features of the synthesis. The macrocyclic lactone ring was created by means of the Yamaguchi procedure. © 2009 Elsevier Ltd. All rights reserved. [-]
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info:eu-repo/semantics/restrictedAccess
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