Literature DB >> 14651104

Total synthesis of (+/-)-acetoxyodontoschismenol using zirconium chemistry.

Ian R Baldwin1, Richard J Whitby.   

Abstract

The dolabellane diterpene (+/-)-acetoxyodontoschismenol has been synthesised for the first time by a short route in which a three component coupling on zirconium is used to assemble all the carbons needed for the skeleton in onepot.

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Year:  2003        PMID: 14651104     DOI: 10.1039/b309848f

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Metallacycle-Mediated Cross-Coupling in Natural Product Synthesis.

Authors:  Natasha F O'Rourke; Matthew J Kier; Glenn C Micalizio
Journal:  Tetrahedron       Date:  2016-09-07       Impact factor: 2.457

2.  Stereoselective total synthesis of parthenolides indicates target selectivity for tubulin carboxypeptidase activity.

Authors:  Robert R A Freund; Philipp Gobrecht; Zhigang Rao; Jana Gerstmeier; Robin Schlosser; Helmar Görls; Oliver Werz; Dietmar Fischer; Hans-Dieter Arndt
Journal:  Chem Sci       Date:  2019-06-26       Impact factor: 9.825

  2 in total

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