Steroids, LII. Configurational Analysis of 16‐Methyl‐19‐nortestosterone Derivatives

Eszter Meskó, György Dombi, Ferenc Lukács, Gyula Schneider

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4 Citations (Scopus)

Abstract

The four possible stereoisomers of 3‐methoxy‐16‐methyloestra‐1,3,5(10)‐trien‐17‐ol (1, 2, 3, 4) were converted into the corresponding 16‐methyl‐19‐nortestosterone analogs (5, 6, 7, 8), which were characterized by their 1H‐ and 13C‐NMR spectra. The coupling constants J16,17 and the characteristic 13C signals (C‐12, C‐17, C‐18, 16‐CH3) clearly confirmed the configurations at C‐16 and C‐17.

Original languageEnglish
Pages (from-to)923-925
Number of pages3
JournalLiebigs Annalen der Chemie
Volume1993
Issue number8
DOIs
Publication statusPublished - 1993

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Stereoisomerism
Steroids

Keywords

  • Steroids

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Steroids, LII. Configurational Analysis of 16‐Methyl‐19‐nortestosterone Derivatives. / Meskó, Eszter; Dombi, György; Lukács, Ferenc; Schneider, Gyula.

In: Liebigs Annalen der Chemie, Vol. 1993, No. 8, 1993, p. 923-925.

Research output: Contribution to journalArticle

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