21-Acetoxy-17α-4-pregnene-3,20-dione
Artikel i vetenskaplig tidskrift, 2005

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.

Författare

Raja Dey

Chalmers, Kemi- och bioteknik

S. Chanda

University of Calcutta

A. Pal

Presidency University

S. Roychowdhury

Presidency University

Acta Crystallographica Section E: Structure Reports Online

1600-5368 (ISSN)

Vol. 61 4

Ämneskategorier

Kemiteknik

DOI

10.1107/S1600536805007415