A rapid formal synthesis of the macrolide (-)-A26771B

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(-)-A26771B, a novel 16-membered macrolide with antibiotic activity, has been formally synthesized. In the synthesis ruthenium catalyzed ring-closing olefin metathesis (RCM) was used as a key reaction to construct the lactone ring. (C) 2001 Elsevier Science Ltd. All rights reserved.
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Issue Date
2001-02
Language
English
Article Type
Article
Keywords

EFFICIENT SYNTHESIS; OLEFIN METATHESIS; ORGANIC-SYNTHESIS; (+)-ASPICILIN; A26771B; ROUTE

Citation

TETRAHEDRON-ASYMMETRY, v.12, no.1, pp.29 - 31

ISSN
0957-4166
DOI
10.1016/S0957-4166(01)00004-0
URI
http://hdl.handle.net/10203/82464
Appears in Collection
CH-Journal Papers(저널논문)
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