Steroids, XLII. Configurational analysis of 3‐methoxy‐16‐methylestra‐1,3,5(10)‐trien‐17‐ol derivatives

Eszter Meskó, G. Schneider, G. Dombi, Dieter Zeigan

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

The four possible isomers of 16‐hydroxymethyl‐3‐methoxyestra‐1,3,5(10)‐trien‐17‐ol 5a, 6a, 7a, 8a were converted into the corresponding 16‐methyl analogues 4a, 11a, 12a, 13a, which were characterized from their 1H‐ and 13C‐NMR spectra. The results permit a configurational correlation with 16‐methyl derivatives reported in the literature.

Original languageEnglish
Pages (from-to)419-422
Number of pages4
JournalLiebigs Annalen der Chemie
Volume1990
Issue number5
DOIs
Publication statusPublished - 1990

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steroids
Isomers
isomers
Steroids
analogs
Derivatives

Keywords

  • Estra‐1,3,5(10)‐trien‐17‐ol derivatives
  • Steroids

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Steroids, XLII. Configurational analysis of 3‐methoxy‐16‐methylestra‐1,3,5(10)‐trien‐17‐ol derivatives. / Meskó, Eszter; Schneider, G.; Dombi, G.; Zeigan, Dieter.

In: Liebigs Annalen der Chemie, Vol. 1990, No. 5, 1990, p. 419-422.

Research output: Contribution to journalArticle

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