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Studies on heterocyclic compounds. VII. Syntheses of novel furo[2, 3-b]chromones
Authors:Sheng-Chu Kuo  Jiin-Sheng Wu  Li-Jiau Huang  Chun-Hsiung Wu  Shun-Chueh Huang  Teh-Chang Chou
Abstract:Furo2, 3-b]chromone ( 1a ) was conveniently prepared by the PPE-promoted cyclization of 5-(2′-carboxy-phenoxy)furan-2-carboxylic acid ( 8 ) which was made from methyl salicylate and ethyl 5-nitrofuran-2-carboxyl-ate. Furo2, 3-b]chromon-2-acrylic acid ( 13 ) was obtained by a similar cyclization. Direct acylation of 1a afforded 2-acetylfuro2, 3-b]chromone ( 10 ). Several derivatives of furo2, 3-b]chromone were found to display activity in the rat passive cutaneous anaphylaxis (PGA) test for antiallergic activity.
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