21-Acetoxy-17α-4-pregnene-3,20-dione

Raja Dey, S. Chanda, A. Pal, S. Roychowdhury

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

The synthetic steroid 21-acetoxy-17α-4-pregnene-3,20-dione, C 23H32O4, crystallizes with a single molecule in the asymmetric unit. The molecule contains four fused rings, typical of steroids. The cyclohexene ring A has nearly the conformation of a boat. One saturated six-membered ring, B, is intermediate between chair and half-chair conformations, while the other six-membered ring, C, is essentially a chair. The five-membered ring D tends towards a twist conformation. The ring junction A/B is quasi-trans, whereas the ring junctions B/C and C/D are both trans. The molecule is slightly convex towards the β side.

Original languageEnglish (US)
Pages (from-to)o980-o982
JournalActa Crystallographica Section E: Structure Reports Online
Volume61
Issue number4
DOIs
StatePublished - Apr 1 2005
Externally publishedYes

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