Literature DB >> 15224330

Synthesis of furano-epothilone D.

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.

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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


  1 in total

1.  Synthesis by ring-closing metathesis and cytotoxic evaluation of novel thienylmacrolactones.

Authors:  Jürgen Krauss; Daniela Köbler; Verena Miller; Franz Bracher
Journal:  Sci Pharm       Date:  2011-11-01
  1 in total

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