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Diosgenin-3,6-dione: second polymorph in space group P2(1)2(1)2(1)

The title steroid, [(25R)-spirost-4-en-3,6-dione, C(27)H(38)O(4)], is obtained by oxidation of diosgenin, using the Jones reagent (CrO(3)/H(2)SO(4)). The crystal structure was previously reported in space group P2(1)2(1)2(1), but nonetheless with the wrong absolute configuration and omitting positio...

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Detalles Bibliográficos
Autores principales: Guerrero-Luna, Gabriel, Reyes Melchor, Jaquelin, Bernès, Sylvain, Hernández-Linares, María-Guadalupe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462274/
https://www.ncbi.nlm.nih.gov/pubmed/36338905
http://dx.doi.org/10.1107/S2414314620012006
Descripción
Sumario:The title steroid, [(25R)-spirost-4-en-3,6-dione, C(27)H(38)O(4)], is obtained by oxidation of diosgenin, using the Jones reagent (CrO(3)/H(2)SO(4)). The crystal structure was previously reported in space group P2(1)2(1)2(1), but nonetheless with the wrong absolute configuration and omitting positions for H atoms [Rajnikant et al. (2000 ▸). Mol. Cryst. Liq. Cryst. Sci. Technol. Sect. C, 12, 101–110]. The diffraction data set reported herein is for a second polymorph in the same space group, as evidenced by simulated powder patterns. Both forms are characterized by a similar ortho­rhom­bic unit cell, and a similar arrangement of the mol­ecules in the crystal structure. However, the conformation of the A/B rings in the steroid nucleus is slightly modified, leading to the observed polymorphism. [Image: see text]