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Abstract
Abstract Photooxygenation of 6-phenyl-5,7-dioxa-benz[a]anthracene in ethanol followed by recrystallization from ethanol resulted in the formation of a diethoxy compound by unusual addition of two ethoxyl groups to a C–C double bond. While, recrystallization of the photooxygenation product from methanol afforded a monoethoxy monomethoxy compound.
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