The title compound, C(29)H(46)O(3), is a steroid synthesized through a rearrangement of a sarsasapogenin derivative in acidic medium. The newly formed ring F is a tetra-hydro-2H-pyran heterocycle substituted by two methyl groups placed in equatorial positions. This ring displays a chair conformation, while di-hydro-furan ring E, to which it is bonded, has an envelope conformation. The mol-ecules are associated by weak O-Hâ¯O hydrogen bonds to form chains running in the [101] direction in the crystal.
(23R,23(1) S,25S)-23(1),26-Ep-oxy-23-ethyl-furost-20(22)-en-3β-ol.
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作者:Guerrero-Luna Gabriel, Hernández-Linares MarÃa-Guadalupe, Cárdenas GarcÃa Maura, Bernès Sylvain
| 期刊: | IUCrdata | 影响因子: | 0.000 |
| 时间: | 2023 | 起止号: | 2023 Apr 21; 8(Pt 4):x230344 |
| doi: | 10.1107/S2414314623003449 | ||
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