The Structure of the Pechmann Condensation Product of p-Orsellinic Acid with Ethyl Acetoacetate

Abstract
The product obtained by the Pechmanr condensation, followed by the decarboxylation, of p-orsellinic acid with ethyl acetoacetate has been established not to be such 4,5-dimethyl-7-hydroxycoumarin as previously reported, but to be 2,5-dimethyl-7-hydroxychromone.

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