A highly efficient synthesis of γ-halo allylic alcohols and propargylic alcohols with high optical purity. Practical method for synthesis of the prostaglandin ω-chain
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (18), 2033-2036
- https://doi.org/10.1016/s0040-4039(00)96038-6
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Prostaglandin synthesis. 10. An extremely short way to prostaglandinsJournal of the American Chemical Society, 1985
- Synthesis of leukotrienes and lipoxygenase productsAccounts of Chemical Research, 1985
- Reduction of .alpha.,.beta.-acetylenic ketones to (S)-propargyl alcohols of high enantiomeric purityThe Journal of Organic Chemistry, 1982
- Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?Journal of the American Chemical Society, 1981
- Reduction of .alpha.,.beta.-acetylenic ketones with B-3-pinanyl-9-borabicyclo[3.3.1]nonane. High asymmetric induction in aliphatic systemsJournal of the American Chemical Society, 1980
- Prostaglandins and congeners. 19. Vinylstannanes: useful organometallic reagents for the synthesis of prostaglandins and prostaglandin intermediatesThe Journal of Organic Chemistry, 1978
- Alkene synthesis via .beta.-functionalized organosilicon compoundsAccounts of Chemical Research, 1977
- Asymmetric reduction. Reduction of acetylenic ketones with chiral hydride agentJournal of the American Chemical Society, 1977
- A tissue-selective prostaglandin E2 analog with potent antifertility effectsCellular and Molecular Life Sciences, 1977
- Reactions of .alpha.,.beta.-epoxysilanes with organocuprate reagents. New stereospecific olefin synthesisThe Journal of Organic Chemistry, 1975