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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2020
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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 |
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] |
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