Issue 7, 1981

Carbonylation of organic halides in the presence of terminal acetylenes; novel acetylenic ketone synthesis

Abstract

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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 333-334

Carbonylation of organic halides in the presence of terminal acetylenes; novel acetylenic ketone synthesis

T. Kobayashi and M. Tanaka, J. Chem. Soc., Chem. Commun., 1981, 333 DOI: 10.1039/C39810000333

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