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Synthesis of furano-epothilone D
Authors:Schinzer Dieter  Bourguet Erika  Ducki Sylvie
Affiliation:Chemisches Institut der Otto-von-Guericke-Universit?t, Universit?tsplatz 2, 39106 Magdeburg, Germany. Dieter.Schinzer@vst.uni-magdeburg.de
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.
Keywords:aldol reactions  antitumor agents  epothilone analogues  macrolides  natural products
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