(25R)-5a-Spirostane-3,12-dione
نویسندگان
چکیده
The title compound, C(27)H(40)O(4), was obtained from the oxidation of (25R)-3b-hydr-oxy-5a-spiro-stan-12-one (Hecogenin) by Jone's reagent. The mol-ecule contains six alicyclic and heterocyclic rings, all trans-fused, among which four six-membered rings adopt similar chair conformations while two five-membered rings assume an envelope conformation.
منابع مشابه
trimethylchlorosilane; cholesterol, Cholest-5-en-3b-ol; oxysterols, cholesterol oxidation products; 7-ketocholesterol, cholest-5-en-3b-ol-7-one; cholestanetriol, cholestan-3b,5a,6b-triol; a-epoxycholesterol, cholestan-5a,6a-epoxy-3b-ol; 25-hydroxycholesterol, cholest-5-en-3b,25-diol; 7a-hydroxycholesterol, Cholest-5-en-3b,7a-diol; 7b- hydroxycholesterol, cholest-5-en-3b,7b-diol; b-epoxycholesterol, cholestan-5b,6b-epoxy-3b-ol; 27-hydroxycholesterol, 25R-cholest-5-en-
Abbreviations : HMDS, 1,1,1,3,3,3-hexamethyldisilazane; TMCS, trimethylchlorosilane; cholesterol, Cholest-5-en-3b-ol; oxysterols, cholesterol oxidation products; 7-ketocholesterol, cholest-5-en-3b-ol-7-one; cholestanetriol, cholestan-3b,5a,6b-triol; a-epoxycholesterol, cholestan-5a,6a-epoxy-3b-ol; 25-hydroxycholesterol, cholest-5-en-3b,25-diol; 7a-hydroxycholesterol, Cholest-5-en-3b,7a-diol; 7b...
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