Synthesis of 14β-cholesta-5,7-dien-3β-ol

Steroids

Volumn 49, Issue 6, 1987, Pages 543-552

  Anastasia, M ^a   Allevi, P ^a   Ciuffreda, P ^a   Fiecchi, A ^a   Scala, A ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

14BETA CHOLESTA 5,7 DIEN 3BETA OL; UNCLASSIFIED DRUG;

DRUG SYNTHESIS; METHODOLOGY;

CHEMISTRY; CHOLESTADIENOLS; DEHYDROCHOLESTEROLS; METHODS; STEREOISOMERISM; SUPPORT, NON-U.S. GOV'T;

EID: 0023632672     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0039-128X(87)90094-8     Document Type: Article

References (17)

1. Stereochemically controlled synthesis of 20-isocholesterol
2. Inversion of the Unnatural cis C/D Sterol Ring Junction of 5alpha, 14beta-Cholest-7-en-3beta-ol by Rat-Liver Enzymes
3. The conversion of cholest-7-en-3beta-ol into cholesterol. General comments on the mechanism of the introduction of double bonds in enzymic reactions.
4. A ready synthesis of 5?,14?-cholest-7-en-3?-ol
5. Synthetic uses of steroidal ring B diene protection: 22,23-dihydroergosterol
6. Unsaturated steroids. Part 7. A simple synthesis of 22,23-dihydroergosterol
7. Retro-1,4-cycloaddition of adducts derived from stereoidal 5,7-dienes and 4-phenyl-1,2,4-triazoline-3,5-dione
8. Mass spectrometry in structural and stereochemical problems. Part CCXX. Synthesis and mass spectra of 5?-cholest-8(9)- and 8(14)-en-7-ones