(25R)-16β-Acetoxy-3β-bromo-23′,26-epoxy-23′,25-dimethyl-5α-cholest-23,23′-en-6-one dichloromethane monosolvate

Autor: Susana Rincón, Rebeca Yépez, M. Eugenia Ochoa, Yliana López, Rosa Santillan, Norberto Farfán
Jazyk: angličtina
Rok vydání: 2012
Předmět:
Zdroj: Acta Crystallographica Section E, Vol 68, Iss 12, Pp o3260-o3261 (2012)
Druh dokumentu: article
ISSN: 16005368
1600-5368
DOI: 10.1107/S1600536812043590
Popis: The crystal structure of the title compound, C31H45BrO5·CH2Cl2, prepared in six steps from diosgenin, confirmed that the configurations of the stereogenic centers, positions 20S and 25R, remain unchanged during the reaction. The six-membered A, B and C rings have chair conformations. The five-membered ring D has an envelope conformation (with the methyl-substituted C atom fused to ring C as the flap) and the six-membered dihydropyran ring E adopts a twist-boat conformation. In the crystal, molecules are linked via C—H...O and C—H...Cl hydrogen bonds, the latter involving the dichloromethane solvent molecule, forming a three-dimensional supramolecular network.
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