Abstract
Abstract The rearrangement of some β-phenoxyethyl alkyl(aryl) ketones to 4-hydroxyphenoxyethyl alkyl(aryl) ketones has been studied. The latter undergo rearrangement under oxidative conditions to flavilium salts such as 0-trimethylapigeninidin chloride or 0-tetramethylluteolinidui chloride. The mechanism of these changes has been discussed.
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