Issue 12, 1994

Stereoselective synthesis of β-lactones containing α-Z-alkoxycarbonylmethylene chains by palladium-catalysed oxidative carbonylation of tertiary α-hydroxyalkynes

Abstract

Tertiary α-hydroxyalkynes undergo oxidative carbonylation in alcohols in the presence of catalytic amounts of Pdl2–Kl to give β-lactones derived from alkoxycarbonylation at the terminal cabon of the alkyne and cis-carbonylation at the internal carbon, followed by carbonyl trapping by the tertiary hydroxy group.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 1429-1430

Stereoselective synthesis of β-lactones containing α-Z-alkoxycarbonylmethylene chains by palladium-catalysed oxidative carbonylation of tertiary α-hydroxyalkynes

B. Gabriele, M. Costa, G. Salerno and G. P. Chiusoli, J. Chem. Soc., Chem. Commun., 1994, 1429 DOI: 10.1039/C39940001429

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