Abstract: We realized the highly selective synthesis of 1,4-disubstituted 1,2,3-triazoles starting from a terminal alkyne and arylazides, without the presence of metal catalyst, using the sequence hydroamination/1,3-dipolar cycloaddition reaction. The structure of synthesized products was determined by the usual spectroscopic
methods (IR, 1H NMR and 13C NMR). The 1,2,3-triazoles obtained were tested for their antimicrobial
properties. Most of them showed a significant antibacterial activity against Pseudomonas aeruginosa,
Citrobacter freundii, Escherichia coli, Staphylococcus aureus, and a fungicidal activity against Aspergillus flavus and Aspergillus ochraceus.
Keywords: alkyne, biological activity, 1,3-dipolar cycloaddition, hydroamination, 1,2,3-triazole
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