A new method for the conversion of aldehydes (RCH2CHO)to acetylenes (RC&.tbnd;CH) via 1-alkenylstannanes. Application to the synthesis of 9(O)-thia-Δ6-PGI1
- 31 December 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (44), 4607-4610
- https://doi.org/10.1016/s0040-4039(00)85666-x
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- A Novel Synthesis of the Sulfur Analog of ∆6-PGI1HETEROCYCLES, 1982
- A new alkyltin (IV)-mediated coupling reaction of aldehydes to olefinsTetrahedron Letters, 1981
- A new, highly efficient method for the conversion of alcohols to thiolesters and thiolsTetrahedron Letters, 1981
- SYNTHESIS OF THE SULFUR ANALOG OF Δ6-PGI1Chemistry Letters, 1980
- Prostaglandins and congeners. 19. Vinylstannanes: useful organometallic reagents for the synthesis of prostaglandins and prostaglandin intermediatesThe Journal of Organic Chemistry, 1978
- Reductive alkylation of aldehyde tosylhydrazones with organolithium reagentsTetrahedron Letters, 1977
- A stereoselective synthesis of (+-)-11-hydroxy-trans-8-dodecenoic acid lactone, a naturally occurring macrolide from Cephalosporium recifeiJournal of the American Chemical Society, 1976
- Nucleophilic ethynyl group equivalent and its use in conjugate addition to .alpha.,.beta.-enonesJournal of the American Chemical Society, 1974
- Vinyl Derivatives of Metals : XVIII. Preparation, characterization and isomerization of propenyl derivatives of silicon, germanium and tinJournal of Organometallic Chemistry, 1963