A highly selective synthesis of versatile (E)-1-phenylthio vinylstannanes
- 1 September 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (38) , 5047-5050
- https://doi.org/10.1016/s0040-4039(00)93424-5
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Transition-Metal-Mediated C-S Bond Cleavage ReactionsSynthesis, 1990
- Et3B induced radical addition of Ph3SnH to acetylenes and its application to cyclization reactionTetrahedron, 1989
- Stereospecific palladium-catalyzed coupling reactions of vinyl iodides with acetylenic tin reagentsJournal of the American Chemical Society, 1987
- Alkenylcopper Derivatives; 271. Synthesis of 1-Alkenyl Thioethers by Cleavage of Disulfides with 1-Alkenyl-copper ReagentsSynthesis, 1985
- Enol thioethers as enol substitutes. An alkylation sequenceJournal of the American Chemical Society, 1983
- Preparation of iodoallylic alcohols via hydrostannylation: spectroscopic proof of structuresTetrahedron Letters, 1982
- Reaction of organotin hydrides with acetylenic alcoholsThe Journal of Organic Chemistry, 1982
- A stereospecific synthesis of cis‐ and trans‐1‐alkenyl sulfides from 1‐alkynyl sulfides and a copper(I) hydride complex or lithium tetrahydridoaluminateRecueil des Travaux Chimiques des Pays-Bas, 1976
- A stereoselective synthesis of (+-)-11-hydroxy-trans-8-dodecenoic acid lactone, a naturally occurring macrolide from Cephalosporium recifeiJournal of the American Chemical Society, 1976
- Organozinnverbindungen, XVII. Hydrostannierung von α-Olefinen mit aluminiumorganischen KatalysatorenEuropean Journal of Organic Chemistry, 1967