Efficient synthesis of a novel estrone-talaromycin hybrid natural product

Lutz F. Tietze, G. Schneider, J. Wölfling, Thomas Nöbel, Christian Wulff, Ingrid Schubert, Angela Rübeling

Research output: Contribution to journalArticle

46 Citations (Scopus)

Abstract

Numerous pharmacologically interesting compounds are available by the synthesis of hybrid natural products. Thus, for instance, the estrone-talaromycin hybrid 2, which is synthesized in a few steps from the estrone derivative 1 by a sequence in which a hetero-Diels-Alder reaction is the key step, exhibits notable cytotoxic activity.

Original languageEnglish
Pages (from-to)2469-2470
Number of pages2
JournalAngewandte Chemie - International Edition
Volume37
Issue number18
DOIs
Publication statusPublished - Oct 2 1998

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Estrone
Biological Products
Derivatives

Keywords

  • Antitumor agents
  • Cycloadditions
  • Mycotoxins
  • Spiro compounds
  • Steroids

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Efficient synthesis of a novel estrone-talaromycin hybrid natural product. / Tietze, Lutz F.; Schneider, G.; Wölfling, J.; Nöbel, Thomas; Wulff, Christian; Schubert, Ingrid; Rübeling, Angela.

In: Angewandte Chemie - International Edition, Vol. 37, No. 18, 02.10.1998, p. 2469-2470.

Research output: Contribution to journalArticle

Tietze, Lutz F. ; Schneider, G. ; Wölfling, J. ; Nöbel, Thomas ; Wulff, Christian ; Schubert, Ingrid ; Rübeling, Angela. / Efficient synthesis of a novel estrone-talaromycin hybrid natural product. In: Angewandte Chemie - International Edition. 1998 ; Vol. 37, No. 18. pp. 2469-2470.
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