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Volumn 57, Issue 33, 2001, Pages 7199-7204
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Highly efficient Lewis acid catalyzed, one step conversions of 16α,17α-epoxy-3β-hydroxypregn-5-en-20-one to D-homosteroid and Δ13-steroids
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Author keywords
13 steroids; D homosteriods; Epoxides; Epoxy steroids; Lewis acids; Rearrangements
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Indexed keywords
13 DELTA STEROID;
16ALPHA,17ALPHA EPOXY 3BETA HYDROXYPREGN 5 EN 20 ONE;
16BETA CHLORO 3BETA,17ALPHA DIHYDROXY 17BETA METHYL 17A HOMOANDROST 5 EN 17A ONE;
3BETA,16ALPHA DIACETOXY 17 METHYL 17ALPHA PREGNA 5,13 DIEN 20 ONE;
ACETIC ANHYDRIDE;
ALPHA CHLOROHYDRIN;
ALUMINUM CHLORIDE;
DEXTRO HOMOSTEROID;
HOMOSTEROID;
STEROID;
UNCLASSIFIED DRUG;
ZINC CHLORIDE;
ARTICLE;
CATALYSIS;
CHEMICAL REACTION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
PRIORITY JOURNAL;
REACTION ANALYSIS;
STEREOCHEMISTRY;
STOICHIOMETRY;
TEMPERATURE;
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EID: 0035855324
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(01)00673-1 Document Type: Article |
Times cited : (14)
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References (46)
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