Literature DB >> 12599465

Diastereoselective titanium enolate aldol reaction for the total synthesis of epothilones.

Guido Koch1, Olivier Loiseleur, Daniel Fuentes, Andrea Jantsch, Karl-Heinz Altmann.   

Abstract

[formula: see text] The development of a highly diastereoselective addition of the titanium enolate derived from ketone 1 to aldehyde 2 offers an efficient entry to the total synthesis of the epothilone family. The new aldol process is robust and tolerates a wide range of functional groups.

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Year:  2002        PMID: 12599465     DOI: 10.1021/ol026480b

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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