An Efficient palladium-catalysed reaction of vinyl and aryl halides or triflates with terminal alkynes
- 1 October 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (40) , 6403-6406
- https://doi.org/10.1016/0040-4039(93)85056-3
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Total Stereocontrolled Synthesis of Lipoxin B4Synlett, 1993
- Palladium-Catalyzed Cross-Coupling Reactions in a Homogeneous Aqueous MediumSynlett, 1992
- An efficient palladium-catalyzed reaction of vinyl chlorides with terminal acetylenesTetrahedron Letters, 1991
- Cross-coupling of organosilanes with organic halides mediated by a palladium catalyst and tris(diethylamino)sulfonium difluorotrimethylsilicateThe Journal of Organic Chemistry, 1988
- Stereospecific palladium-catalyzed coupling reactions of vinyl iodides with acetylenic tin reagentsJournal of the American Chemical Society, 1987
- Nickel- or palladium-catalyzed cross coupling. 31. Palladium- or nickel-catalyzed reactions of alkenylmetals with unsaturated organic halides as a selective route to arylated alkenes and conjugated dienes: scope, limitations, and mechanismJournal of the American Chemical Society, 1987
- A general and stereocontrolled total synthesis of leukotriene B4 and analogsJournal of the American Chemical Society, 1984
- Stereoselective preparation of 1-chloro-(E,E)-1,3-dienes. Application to the synthesis of methyl eleostearate.Tetrahedron Letters, 1984
- New Synthesis of the Sex Pheromone of the Egyptian Cotton Leafworm, Spodoptera LittoralisSynthetic Communications, 1981
- Synthesis of aryl- and vinyl-substituted acetylene derivatives by the use of nickel and palladium complexesJournal of Organometallic Chemistry, 1975