A new series of ketoazomethines were synthesized by condensation of phenyl glyoxal (prepared by partial oxidation of acetophenone) with various p-substituted anilines viz. p-Cl, p-Br, p-NO2, p-(C2H5) 2N and p-CH3. These compounds were characterized by elemental analysis, IR and H1 NMR. The synthesized ketoazomethines were screened for their antifungal acsutivity against hazardous fungi namely Fusarium oxysporum, Alternaria ...
