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Synthesis and biological evaluation of new benzo[f]furo[2,3‐h]‐and benzo[f]pyrano[2,3‐h]coumarin derivatives.
Authors:Maria Tsoukka  Konstantinos E. Litinas  Demetrios N. Nicolaides  Dimitra J. Hadjipavlou‐Litina
Affiliation:1. Laboratory of Organic Chemistry, Department of Chemistry, Aristotle University of Thessaloniki, Thessaloniki 54124 Greece;2. Laboratory of Organic Chemistry, Department of Chemistry, Aristotle University of Thessaloniki, Thessaloniki 54124, Greece
Abstract: chemical structure image Furocoumarins 3,5 and pyranocoumarin 7 were synthesized from the reaction of furonaphthalenediones 2,4 and pyranonaphthalenedione 6 respectively with carbethoxymethylene(triphenyl)phosphorane in refluxing DCM for 3‐6 hours or under microwave irradiation in toluene for a few minutes. Compounds 3,5,7 and their precursors were tested as anti‐inflammatory/antioxidant agents. They were found to compete significantly high DMSO for OH radicals, to scavenge O2? and to inhibit lipoxygenase to a high extent.
Keywords:
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