Detalhes do Documento

3-Oxoandrosta-4,6-dien-17[beta]-yl 2-methyl-1H-imidazole-1-carboxylate and 3-ox...

Autor(es): Silva, Manuela Ramos cv logo 1 ; Moreira, Vânia M. cv logo 2 ; Cardoso, Cláudia cv logo 3 ; Beja, Ana Matos cv logo 4 ; Salvador, Jorge A. R. cv logo 5

Data: 2009

Identificador Persistente: http://hdl.handle.net/10316/12970

Origem: Estudo Geral - Universidade de Coimbra


Descrição
The title compounds, C24H30N2O3, (I), and C24H34N2O3, (II), both contain an androstane backbone and a 2-methylimidazole-1-carboxylate moiety at the 17-position. Compound (I) contains two symmetry-independent molecules (denoted 1 and 2), while compound (II) contains just one molecule in the asymmetric unit. The C-C-O-C torsion angle that reflects the twisting of the 2-methylimidazole-1-carboxylate moiety from the mean steroid plane is 143.1 (2)° for molecule 1 of (I), 73.1 (3)° for molecule 2 of (I) and 86.63 (17)° for (II). The significance of this study lies in its observation of significant differences in both molecular conformation and supramolecular aggregation between the molecules of the title compounds. The solid-state conformations compared with those obtained theoretically from ab initio methods for the isolated molecules show large differences, especially in the orientation of the methylimidazole substituent
Tipo de Documento Artigo
Idioma Inglês
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