Issue 13, 1988

Furan-3(2H)-ones by tandem photo-oxidation–intramolecular Michael addition

Abstract

Photo-sensitized oxygenation of the furyl diketones (1) affords furan-3(2H)-ones (3) in satisfactory yields, presumably via the intermediate open-chain enetriones (2).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 850-851

Furan-3(2H)-ones by tandem photo-oxidation–intramolecular Michael addition

R. Antonioletti, F. Bonadies, T. Prencipe and A. Scettri, J. Chem. Soc., Chem. Commun., 1988, 850 DOI: 10.1039/C39880000850

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