Author/Authors :
Libero، نويسنده , , Francieli M. and Xavier، نويسنده , , Maurيcio C.D. and Victoria، نويسنده , , Francine N. and Nascente، نويسنده , , Patrيcia S. and Savegnago، نويسنده , , Lucielli and Perin، نويسنده , , Gelson and Alves، نويسنده , , Diego، نويسنده ,
Abstract :
We describe herein the synthesis and antifungal activity of new 5-arylchalcogenoalkyl-1H-tetrazoles 4. Arylchalcogenoalkyl-1H-tetrazoles 4 have been synthesized in high yields by reaction of arylchalcogenolate anions with chloronitriles 2, and subsequent [2+3] cycloaddition of resulting arylchalcogenoalkylnitriles 3 with sodium azide by zinc catalysis in aqueous solution. The obtained compound 4a was screened for antifungal activity and presented inhibitory property against seven fungal strains. This protocol is an efficient method to produce new selenium–nitrogen compounds with antifungal activity.
Keywords :
1H-Tetrazoles , Antifungal , Organochalcogen compounds , Nitriles , cycloaddition