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Carbonylation of organic halides in the presence of terminal acetylenes; novel acetylenic ketone synthesis
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1981
Year
HalogenationChemical EngineeringCross-coupling ReactionEngineeringOrganic HalidesNovel OrganocatalystsOrganic ChemistryTerminal AcetylenesCatalysisVinylic HalidesChemistryStereoselective SynthesisAcetylenic Ketone SynthesisOrganometallic CatalysisAsymmetric CatalysisEnantioselective SynthesisCarbon Monoxide
Aryl, heterocyclic, and vinylic halides react with carbon monoxide and terminal acetylenes at 120 °C or below and 80 atm or below in the presence of triethyl-amine and a catalytic amount of a palladium (II) complex to form acetylenic ketones in 46·7–92·9% yield.