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   <subfield code="a">Electrophilic heterocyclization of 4,5-disubstituted 3-allylthio-4 H -1,2,4-triazoles by the action of halogens</subfield>
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   <subfield code="a">A study was carried out on the regioselectivity of the electrophilic heterocyclization of 4,5-disubstituted 3-allylthio-4H-1,2,4-triazoles by the action of bromine and iodine. Factors affecting the halogenation regioselectivity, namely, the nature of the electrophilic reagent and the presence of lithium perchlorate, were studied. A method was developed to obtain 5,6-dihydro-3H-[1,3]thiazolo[3,2-b]triazolium salts. The structure of these salts was confirmed by spectral methods and chemical transformations.</subfield>
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