Issue 20, 1980

Synthesis of 4,4-disubstituted cyclohexenones by the Baeyer–Villiger fragmentation of 1-methoxybicyclo[2.2.2]oct-5-enones

Abstract

The sodium acetate-buffered, peracetic acid oxidation of various 1-methoxybicyclo[2.2.2]oct-5-enones, prepared by hydrolysis of the adducts derived from dihydroanisole derivatives and α-chloroacrylonitrile, leads to 4-substituted cyclohex-2-en-1-one 4-acetic acid derivatives.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 956-957

Synthesis of 4,4-disubstituted cyclohexenones by the Baeyer–Villiger fragmentation of 1-methoxybicyclo[2.2.2]oct-5-enones

N. C. Madge and A. B. Holmes, J. Chem. Soc., Chem. Commun., 1980, 956 DOI: 10.1039/C39800000956

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