Issue 18, 1983

Cyclisation of alkynecarboxylic acids: a route to an oxaspirolactone

Abstract

Pent-4-yonic acid, in various alcohols, was cyclised in the presence of yellow mercury(II) oxide to 4,5-dihydro-5-alkoxy-5-methylfuran-2(3H)-ones; 8-hydroxyoct-4-yonic acid was also cyclised in dimethylformamide to 1,6-dioxaspiro[4.5]decan-2-one in good yield.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 991-992

Cyclisation of alkynecarboxylic acids: a route to an oxaspirolactone

M. Yamamoto, M. Yoshitake and K. Yamada, J. Chem. Soc., Chem. Commun., 1983, 991 DOI: 10.1039/C39830000991

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