Fig. 1From: Antiplasmodial dihetarylthioethers target the coenzyme A synthesis pathway in Plasmodium falciparum erythrocytic stagesStructures and syntheses of 1,3,4-oxadiazole-containing dihetarylthioethers 3. Compounds 3a–m were commercially available. Reagents and conditions for 3n–q: i triethylamine, DMF or propan-2-ol, 90–120 °C. 3r and 3s were synthesized from 3n and 3o respectively by cleavage of the protecting group with trifluoroacetic acid in dichloromethaneBack to article page