Benzo-annulated steroids: Synthesis of octahydro-indeno-phenanthrenes by formal [3+3] cyclocondensation reaction with 1,3-Bis[(trimethylsilyl)oxy]buta-1, 3-dienes

Friedrich Erben, Verena Specowius, János Wölfling, Gyula Schneider, Peter Langer

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Octahydro-indeno-phenanthrenes, benzo-annulated steroids, were prepared by formal [3+3] cyclocondensation reaction of 1,3-bis[(trimethylsilyl)oxy]buta-1,3- dienes with the silyl enol ether of 16-formylestrone methyl ether.

Original languageEnglish
Pages (from-to)924-930
Number of pages7
JournalHelvetica Chimica Acta
Volume96
Issue number5
DOIs
Publication statusPublished - May 1 2013

Keywords

  • Cyclocondensation
  • Estrone
  • Indenophenanthrenes
  • Steroids

ASJC Scopus subject areas

  • Catalysis
  • Biochemistry
  • Drug Discovery
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

Fingerprint Dive into the research topics of 'Benzo-annulated steroids: Synthesis of octahydro-indeno-phenanthrenes by formal [3+3] cyclocondensation reaction with 1,3-Bis[(trimethylsilyl)oxy]buta-1, 3-dienes'. Together they form a unique fingerprint.

  • Cite this