Facile and stereoselective synthesis of 25-hydroxyvitamin d2
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (31), 3347-3350
- https://doi.org/10.1016/s0040-4039(01)81381-2
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Stereoselective synthesis of (23S,25R)-23,25,26-trihydroxyvitamin D3 and (23S,25R)-25-hydroxyvitamin D3 26,23-lactol, presumed vitamin D3 metabolitesThe Journal of Organic Chemistry, 1982
- Stereoselective synthesis and structure proof of a metabolite of vitamin D3, (23S,25R)-25-hydroxyvitamin D3 26,23-lactone (calcidiol lactone).CHEMICAL & PHARMACEUTICAL BULLETIN, 1981
- Asymmetric epoxidation provides shortest routes to four chiral epoxy alcohols which are key intermediates in syntheses of methymycin, erythromycin, leukotriene C-1, and disparlureJournal of the American Chemical Society, 1981
- The influence of chain-branching on the steric outcome of some olefin-forming reactionsJournal of the Chemical Society, Perkin Transactions 1, 1980
- Scope and stereochemistry of an olefin synthesis from β-hydroxysulphonesJournal of the Chemical Society, Perkin Transactions 1, 1978
- Calciferol and its relatives. Part 23. An alternative synthesis of Windaus and Grundmann's C19 ketoneJournal of the Chemical Society, Perkin Transactions 1, 1978
- Metabolism and Mechanism of Action of Vitamin DAnnual Review of Biochemistry, 1976
- Biological activity of 1,25-dihydroxyvitamin D2 in the chickBiochemistry, 1976
- Reactions of lithium diorganocuprates(I) with oxiranesThe Journal of Organic Chemistry, 1973
- Isolation and identification of 25-hydroxyergocalciferolBiochemistry, 1969