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Different thiosemicarbazone derivatives react with dimethyl acetylene dicarboxylate (DMAD) and diethyl acetylene dicarboxylate (DEAD) by three different methods: a) in ethyl acetate solvent at ambient temperature, b) one-pot synthesis under microwave irradiation and solventfree conditions (three-component reaction between thiosemicarbazide, aldehyde/ ketone and DMAD or DEAD), c) a microwave-assisted synthesis under solvent-free conditions, to obtain five-membered S,N-heterocycles thiazolines in good to excellent yields.

Some pentafluoropyridine derivatives have been synthesized by the reaction of pentafluoropyridine with appropriate mono and bidentate nucleophile under ultrasonic irradiation. This new methodology provides good to excellent yields in short reaction times (25-120 min) at room temperature.

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