Abstract An efficient one-pot, convenient catalysis for the synthesis of 5-substituted-1H- tetrazoles is reported. The [3+ 2] cycloaddition involves various nitriles, sodium azide in refluxing DMF and AgNO 3 as catalyst to give corresponding 5-substituted-1H-tetrazoles in good to excellent yields. It is expected that the reaction proceeds via in situ formation of a silver azide species, which participates in coordination of nitrile moiety followed by ...