Abstract

The reaction of o-aminophenol with 4- and 4′-substituted chalcones and benzalacetones in methanol (with a tertiary amine as the catalyst), which leads to products of β addition of 2-aminophenoxazin-3-one to the C=C bond of an unsaturated ketone, was investigated. The activating role of the unsaturated ketone in the formation of a phenoxazine fragment was examined. The structures of the synthesized compounds were confirmed by IR, UV, PMR, and mass spectrometry.

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