Facile Synthesis of the Chalcones and Dihydrochalcones from Naringin, Neohesperidin and Hesperidin

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Abstract
The flavanone glycosides naringin, neohesperidin and hesperidin were converted chemically to the corresponding chalcones and dihydrochalcones; the one-step synthesis, performed at room temperature, required the presence of 25% KOH in the reaction mixture for the former and 10% KOH, a catalyst and molecular hydrogen at atmospheric pressure for the latter.

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