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Egyptian Journal of Pharmaceutical Sciences. 1997; 38 (4-6): 271-280
in English | IMEMR | ID: emr-44547

ABSTRACT

In this study, new series of thiazolidinones 3a-e was synthesized by the cyclocondensation of the Schiff bases 2a-e with mercaptoacetic acid. The thiadiazole 5 was obtained by refluxing 4 with carbondisulfide. The antischistosomal activity was determined for the new representative compounds


Subject(s)
Thiadiazoles/pharmacology , Thiazoles/chemical synthesis , Schistosomicides/chemical synthesis
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