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Homogeneous palladium-catalysed arylation of activated alkenes with aryl chlorides
Authors:Alwyn Spencer
Affiliation:Central Research Laboratories, Ciba-Geigy AG, CH-4002 Basel Switzerland
Abstract:A study has been made of arylation of activated alkenes with aryl chlorides homogeneously catalysed by palladium acetate in the presence of triphenylphosphine or tri-p-tolylphosphine. Electron-withdrawing substituents in the aryl chloride favour the reaction. Only moderate yields could be obtained, and the maximum turnover number was 51, mainly because of precipitation of palladium metal. The probable mechanism of the reaction is discussed.
Keywords:Authors to whom correspondence should be addressed.
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