| Literature DB >> 15224330 |
Dieter Schinzer1, Erika Bourguet, Sylvie Ducki.
Abstract
The total synthesis of furano-epothilone D by a convergent route is reported. The key fragments are available on a large scale to provide sufficient material for biological evaluation. The approach involves a palladium-catalyzed coupling that generates a highly functionalized aldehyde which is connected in a stereoselective aldol reaction to yield the framework of furano-epothilone D. Finally, a macrolactonization provides furano-epothilone D.Entities:
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Year: 2004 PMID: 15224330 DOI: 10.1002/chem.200400125
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236