Tetrahedron p. 4387 - 4410 (1997)
Update date:2022-08-05
Topics:
Mitchell, Anthony S.
Russell, Richard A.
The oxidation of substituted phenols with phenyliodonium diacetate in methanol was found to afford 2,4-cyclohexadienones, 2,5-cyclohexadienones or mixtures of isomers, depending on the substrate being oxidized. Annulation of these cyclohexadienones with the anion of 3-cyanophthalide afforded anthraquinones in high yields.
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