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Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst
Journal of the Chemical Society Chemical Communications · 1979 · pp. 866–866
Abstract
The reaction of aryl halides with alk-l-enylboranes, readily obtainable via monohydroboration of acetylenes, provides a conveninet new method for stereoselective synthesis of arylated (E)-alkenes in high yields; these reactions are effectively catalysed by tetrakis(triphenylphosphine)palladium and bases such as sodium ethoxide.
Organoboron and organosilicon chemistryChemical Synthesis and ReactionsCatalytic Cross-Coupling ReactionsChemistryArylHalideStereoselectivityTriphenylphosphinePalladiumCatalysisSodium ethoxideOrganic chemistryCombinatorial chemistry
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