Journal of the Chemical Society. Perkin transactions I p. 747 - 749 (1983)
Update date:2022-07-30
Topics:
Amupitan, Joseph A.
Huq, Enamul
Mellor, Michael
Scovell, Edward G.
Sutherland, James K.
A series of C-2 substituted 3-methylcyclohex-2-enones has been prepared using the Hagemann ester route.A new synthesis of these compounds has been developed which involves the alkylation of the N,N-diethylaminoethyl ether of 1-hydroxy-5-methylcyclohexa-1,5-diene.The cyclohexenones have been converted into the corresponding α,β-epoxyketones using alkaline hydrogen peroxide.
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