Literature DB >> 11440584

Total synthesis of epothilones B and D.

R E Taylor1, Y Chen.   

Abstract

[reaction: see text] A highly convergent total synthesis of the natural products epothilone B and D is described. The route is highlighted by efficient generation of a C12-C13 trisubstituted olefin which exploits a sequential Nozaki-Hiyama-Kishi coupling and a stereoselective thionyl chloride rearrangement.

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Year:  2001        PMID: 11440584     DOI: 10.1021/ol010094x

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  New sources of chemical diversity inspired by biosynthesis: rational design of a potent epothilone analogue.

Authors:  Jeffrey D Frein; Richard E Taylor; Dan L Sackett
Journal:  Org Lett       Date:  2009-08-06       Impact factor: 6.005

2.  Synthesis and Biological Evaluation of 7-Deoxy-Epothilone Analogues.

Authors:  Laura M Woods; Joseph W Arico; Jeffrey D Frein; Dan L Sackett; Richard E Taylor
Journal:  Int J Mol Sci       Date:  2017-03-17       Impact factor: 5.923

  2 in total

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