Nitrile oxides generated in situ by the oxidative dehydrogenation of aromatic aldoximes (1a-g) undergo 1,3-dipolar cycloaddition reaction with 3-(4-methoxyphenyl)propiolonitrile (2) to afford the new cycloadducts 3-aryl-5-(4- methoxyphenyl)-isoxazole-4-carbonitriles (3a-g) in moderate yield. The new synthesized cycloadducts were tested for their antifungal and antibacterial activity.
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