Тиетанильная защита в синтезе 5-арилокси (сульфонил) -3-бром-1,2,4-триазолов, nucleophilic substitution of the 5-bromine atom by phenoxy or phenylsulfanyl group, oxidation of the thietane

and subsequent nucleophilic substitution reaction of the latter with the bromine atom.

of the reaction products. The possible reaction products were determined by NMR spectroscopy, mass spectrometry

spectroscopy data. The compounds synthesized here had potentially high antiaggregatory activity.

spectroscopy. The synthesized compounds exhibited antidepressant activity.

were confirmed using IR and PMR spectroscopy. The synthesized compounds exhibited anti

were confirmed using IR and PMR spectroscopy. The synthesized compounds exhibited anti

. The structures of the synthesized compounds were confirmed by IR, PMR, and 13C and 15N NMR spectroscopy

. The structures of the synthesized compounds were confirmed by IR, PMR, and 13C NMR spectroscopy and GC-MS data

. The structures of the synthesized compounds were established by IR, PMR, and 13C NMR spectroscopy. In vitro