Acta Cryst. (2005). E61, o160-o162  [ doi:10.1107/S1600536804033173 ]

17-Allyl-16,17a-dioxo-17-aza-D-homoestra-1,3,5(10)-trien-3-yl acetate

R. Hema, V. Parthasarathi, R. Bansal and A. Linden

Abstract: In the title compound, C₂₃H₂₇NO₄, a modified synthetic D-homo steroid, the cyclohexene ring adjacent to the aromatic ring adopts a half-chair conformation, while the cyclohexane ring has an ideal chair conformation and the heterocyclic ring has a sofa conformation. The plane of the allyl substituent lies almost perpendicular to the least-squares plane of the heterocyclic ring. The crystal structure contains a series of weak C-HO intermolecular interactions.

Online 24 December 2004

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