Abstract
AbstractA regioselective synthesis of 3‐pyrazolyl‐4‐aryl substituted pyrrole derivatives from α‐aroylidineketene dithioacetals using a convenient and efficient protocol. The pyrrolylpyrazole molecules were expected to have good application in biological system consequently most of the compounds shows excellent antibacterial activity when compared with streptomycin drug. All the synthesized compounds were studied for their anticancer activity in which 5 b, 5 e, 5 g, 5 i have cytotoxic potential on cervical cancer cells at lower concentration.
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