Terminal alkyne dicarbonylation can be readily effected under mild conditions by treating alkynes with carbon monoxide and alcohols or water at 25-80°C in the presence of Pdlp, KI and air, with unprecedented catalytic efficiency. Dicarbonylated products are mainly maleic esters or acids and their ring-chain tautomers. The latter are formed to a large extent at room temperature. Reaction pathways are discussed.

An efficient and selective palladium-catalysed oxidative dicarbonylation of alkynes to alkyl- or aryl-maleic esters

GABRIELE, Bartolo;
1994

Abstract

Terminal alkyne dicarbonylation can be readily effected under mild conditions by treating alkynes with carbon monoxide and alcohols or water at 25-80°C in the presence of Pdlp, KI and air, with unprecedented catalytic efficiency. Dicarbonylated products are mainly maleic esters or acids and their ring-chain tautomers. The latter are formed to a large extent at room temperature. Reaction pathways are discussed.
Carbonylation; Alkynes; Palladium
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/20.500.11770/146749
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