Abstract: | 5-(p-Acetylphenyl)-2-phenyloxazole ( I ) was condensed with aromatic aldehydes to furnish chalcones 2a-e . Cyclocondensation of 2a-e with hydrazine hydrate and with phenyl hydrazine led to the formation of pyrazoline derivatives 3a-e and 4a-e respectively. Similarly, 2a was interacted with hydroxylamine to give isoxazoline ( 5 ). On the other hand, condensation of 1 with phenyl hydrazine yielded hydrazone 6 which on treatment with Vilsmeier reagent (DMF/POCl3) gives 5-[p-(4-formyl-1-phenylpyrazol-3-yl)phenyl]-2-phenyloxazole ( 7 ). Also, a few derivatives of 7 have been prepared. Moreover, all compounds were screened for their antimicrobial activity against some strains of bacteria and fungi. |