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Design and synthesis of constrained epothilone analogs: The efficient synthesis of eleven-membered rings by olefin metathesis

✍ Scribed by Jeffrey D. Winkler; Joanne M. Holland; Jiri Kasparec; Paul H. Axelsen


Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
983 KB
Volume
55
Category
Article
ISSN
0040-4020

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✦ Synopsis


The efficient synthesis of both left-and right-hand halves of a constrained analog of the anticancer natural product epothilone is described. The eleven-membered rings common to both compounds are prepared by olefin metathesis.


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