Stereocontrolled synthesis of steroid side chains via organoboranes. Stereospecific synthesis of 20R- and 20S-25-hydroxycholesterol.
- 31 December 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (20) , 2077-2080
- https://doi.org/10.1016/s0040-4039(00)87265-2
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Stereoselective Introduction of Steroid Side Chains at C (17) and C (20)Helvetica Chimica Acta, 1981
- C-20 Stereospecific introduction of a steroid side chainJournal of the American Chemical Society, 1981
- Stereocontrolled synthesis of a steroid side chainThe Journal of Organic Chemistry, 1981
- Regio-controlled coupling of (.pi.-allyl) palladium complexes with organozirconium species: a new steroid synthesisJournal of the American Chemical Society, 1980
- Stereochemically controlled synthesis of steroid side chains: synthesis of desmosterolThe Journal of Organic Chemistry, 1980
- Synthesis of 21-hydroxycholesterol and 25-hydroxycholesterol from 3β-hydroxyandrost-5-en-17-one. A method for the stereospecific construction of sterol side-chainsJournal of the Chemical Society, Perkin Transactions 1, 1978
- Stereocontrolled synthesis of the ecdysone side chain via organopalladium chemistryThe Journal of Organic Chemistry, 1977
- Trimethylsilylpotassium. Deoxygenation of epoxides with inversion of stereochemistryJournal of the American Chemical Society, 1976
- Vitamin D3 Metabolites I. Synthesis of 25‐hydroxycholesterolHelvetica Chimica Acta, 1974
- Umwandlung des Dehydro‐androsterons in 17‐ iso ‐Progesteron und ProgesteronBerichte der deutschen chemischen Gesellschaft (A and B Series), 1939