The synthesis describes interaction of triazoles with carbonium ions, suggesting regioselectivity is influenced by substituents.
1-Adamant-1-yl-4-phenyl-1H-1,2,3-triazole and 2-adamant-1-yl-4,5-diphenyl-2H-1,2,3-triazole were synthesized by alkylation in strong proton acids as well as by 1,3-dipolar cycloaddition. It was shown that the regioselectivity of the interaction of NH-unsubstituted 1,2,3-triazoles with the carbonium ion has been determined by the presence and nature of the substituent at the endocyclic carbon atoms
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Mazhai et al. (2025) studied this question.
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