Total synthesis and biological evaluation of (-)-englerin A and B : Synthesis of analogues with improved activity profile

Research output: Journal Publications and Reviews (RGC: 21, 22, 62)21_Publication in refereed journalpeer-review

72 Scopus Citations
View graph of relations

Author(s)

  • Lea Radtke
  • Matthieu Willot
  • Slava Ziegler
  • Stephanie Sauerland
  • Carsten Strohmann
  • Roland Fröhlich
  • Peter Habenberger
  • Herbert Waldmann
  • Mathias Christmann

Detail(s)

Original languageEnglish
Pages (from-to)3998-4002
Journal / PublicationAngewandte Chemie - International Edition
Volume50
Issue number17
Publication statusPublished - 18 Apr 2011
Externally publishedYes

Abstract

The large-scale synthesis of englerin A (see scheme) and subsequent structure-activity relationship studies have led to the discovery of highly potent analogues. TBS=tert-butyldimethylsilyl. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Research Area(s)

  • guaianes, renal cancer, structure-activity relationships, terpenes, total synthesis

Citation Format(s)

Total synthesis and biological evaluation of (-)-englerin A and B: Synthesis of analogues with improved activity profile. / Radtke, Lea; Willot, Matthieu; Sun, Hongyan et al.
In: Angewandte Chemie - International Edition, Vol. 50, No. 17, 18.04.2011, p. 3998-4002.

Research output: Journal Publications and Reviews (RGC: 21, 22, 62)21_Publication in refereed journalpeer-review