The palladium-catalysed arylation of activated alkenes with aroyl chlorides
HU Blaser, A Spencer
Index: Blaser, Hans-Ulrich; Spencer, Alwyn Journal of Organometallic Chemistry, 1982 , vol. 233, # 2 p. 267 - 274
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Citation Number: 131
Abstract
Abstract Aroyl chlorides react with activated alkenes in presence of a tertiary amine and a catalytic amount of palladium acetate to give arylated alkenes, specifically cinnamic acid derivatives and stilbenes. The reaction involves a highly efficient decarbonylation of the aroyl chloride. High yields can be obtained at low catalyst concentration by choice of an appropriate base. The reaction is not particularly sensitive to substituents in the aroyl ...
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