Design and synthesis of constrained epothilone analogs: The efficient synthesis of eleven-membered rings by olefin metathesis
β 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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β¦ 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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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
The investigation of palladium-catalyzed alkoxyallylation of activated olefins, followed by ring-closing metathesis to synthesize functionalized seven-membered ring allyl ethers is described. The influence of the olefin substituents on the diastereoselectivity of the alkoxyallylation has also been e