17-oxo-13α-androst-5-en-3β-yl acetate

G. Bunkóczi, J. A. Cuesta-Seijo, Á Szájli, G. Schneider, J. Wölfling

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

The title compound, C21H30O3 was synthetized by the epimerization of 17-oxoandrost-5-en-3β-yl acetate. There are four fused rings. The A/E and B/C ring fusions are trans, whereas the C/D ring fusion is cis. Rings A and C adopt chair conformations, ring B a distorted half-chair conformation and ring D a 14β-envelope conformation.

Original languageEnglish
JournalActa Crystallographica Section E: Structure Reports Online
Volume62
Issue number11
DOIs
Publication statusPublished - Nov 2006

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Conformations
acetates
Acetates
rings
Fusion reactions
seats
fusion
envelopes

ASJC Scopus subject areas

  • Condensed Matter Physics
  • Structural Biology

Cite this

17-oxo-13α-androst-5-en-3β-yl acetate. / Bunkóczi, G.; Cuesta-Seijo, J. A.; Szájli, Á; Schneider, G.; Wölfling, J.

In: Acta Crystallographica Section E: Structure Reports Online, Vol. 62, No. 11, 11.2006.

Research output: Contribution to journalArticle

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