Syntheses and absolute structures of novel protein farnesyltransferase inhibitors, kurasoins A and B.

نویسندگان

  • T Sunazuka
  • T Hirose
  • Z M Tian
  • R Uchida
  • K Shiomi
  • Y Harigaya
  • S Omura
چکیده

(70% of theory) and >90% ee, as determined by NMR analysis of the derived ( + )-MTPA ester.5) Protection of (-)-6 by TBSC1 and imidazole afforded (-)-7f in 71% yield. Stereospecific alkylation of epoxide (-)-7 with phenylmagnesium bromide in the presence of Cul afforded the (-)-8f in 75% yield. Moffat oxidation (DCC, TFA, pyridine, DMSO, benzene) of (-)-8 furnished (-)-9t (88%). Finally, removal of the TBS group

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منابع مشابه

Kurasoins A and B, new protein farnesyltransferase inhibitors produced by Paecilomyces sp. FO-3684. II. Structure elucidation and total synthesis.

The structures of new protein farnesyltransferase inhibitors, kurasoins A and B, were elucidated by NMR study. Kurasoins A and B are acyloin compounds having in common a 3-hydroxy-1-phenyl-2-butanone moiety, to which p-hydroxyphenyl and 3-indolyl moieties respectively, are connected at C-4. The structures were confirmed by total synthesis.

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Kurasoins A and B, new protein farnesyltransferase inhibitors produced by Paecilomyces sp. FO-3684. I. Producing strain, fermentation, isolation, and biological activities.

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عنوان ژورنال:
  • The Journal of antibiotics

دوره 50 5  شماره 

صفحات  -

تاریخ انتشار 1997