Biosynthetic studies of marine lipids. 4. Mechanism of side chain alkylation in E-24-propylidenecholesterol by a Chrysophyte alga
- 1 October 1984
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 49 (20) , 3742-3752
- https://doi.org/10.1021/jo00194a014
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- 24‐Isopropylcholesterol and 22‐Dehydro‐24‐isopropylcholesterol, Novel Sterols from a SpongeHelvetica Chimica Acta, 1979
- Stereoselective enzymatic O-methylation of tetrahydropapaveroline and tetrahydroxyberbine alkaloidsBiochemical Pharmacology, 1979
- Dinosterol side chain biosynthesis in a marine dinoflagellate, Crypthecodinium cohniiPhytochemistry, 1979
- Metabolism of Δ24-sterols by yeast mutants blocked in removal of the C-14 methyl groupCanadian Journal of Biochemistry, 1978
- Identification of C-24 alkyl epimers of marine sterols by 13C nuclear magnetic resonance spectroscopyCanadian Journal of Chemistry, 1978
- Lanthanide- and aromatic solvent-induced shift effects on proton resonances in C-4-methylated steroids and tetracyclic triterpenoidsChemistry and Physics of Lipids, 1977
- Yeast mutants blocked in removing the methyl group of lanosterol at C-14. Separation of sterols by high-pressure liquid chromatographyBiochemistry, 1977
- Mechanism of Carbon Isotope Fractionation Associated with Lipid SynthesisScience, 1977
- Check-list of British marine algae-third revisionJournal of the Marine Biological Association of the United Kingdom, 1976
- Protonenresonanzspektrosopie und Steroidstruktur. II. Die Lage der C‐18‐ und C‐19‐Methylsignale in Abhängigkeit von den Substituenten am SteroidgerüstHelvetica Chimica Acta, 1962