The Reversibility of the Isomerization of the Δ8 to Δ7 Bond in Cholesterol Biosynthesis
- 1 October 1974
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 48 (1) , 263-269
- https://doi.org/10.1111/j.1432-1033.1974.tb03764.x
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- The incorporation of a hydrogen atom at C-15 of cholesterol biosynthesized from squaleneBiochemical Journal, 1969
- The reversibility of the Δ8-cholestenol–Δ7-cholestenol isomerase reaction in cholesterol biosynthesisBiochemical Journal, 1969
- The stereochemistry of hydrogen elimination in the biological conversion of 5α-cholest-8-en-3β-ol to 5α-cholest-7-en-3β-olSteroids, 1968
- Mass spectrometric investigations of some unsaturated sterols biosynthetically related to cholesterolSteroids, 1967
- Enzymatic isomerization (Δ8 → Δ7) of intermediates of sterol biosynthesisSteroids, 1966
- Mas Spectrometry in Structural and Stereochemical Problems. XXIV.1 A Study of the Hydrogen Transfer Reactions Accompanying Fragmentation Processes of 11-Keto Steroids. Synthesis of Deuterated Androstan-11-ones2Journal of the American Chemical Society, 1963
- The action of perphthalic acid on 5-dihydroergosteryl and ergosteryl acetatesJournal of the Chemical Society, 1954
- Cholesterol and Companions. III. Cholestanol, Lathosterol and Ketone 104Journal of the American Chemical Society, 1953
- 158. The application of the method of molecular rotation differences to steroids. Part IV. Optical anomaliesJournal of the Chemical Society, 1948
- The Dehydration of the 7-Epimeric 3(β)-Acetoxycholestanols-7. Some Transformation Products of γ-CholestenolJournal of the American Chemical Society, 1943