Journal of the Chemical Society. Chemical communications p. 224 - 225 (1981)
Update date:2022-08-04
Topics:
Schultz, Arthur G.
Napier, James
The base-catalysed rearrangement of the 2-aryloxycyclohex-2-enone (3) to the enone (4a) is suggested to occur by an enolate-promoted 3,3-sigmatropic rearrangement of the enolate aryl ether (7).
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