Click Synthesis of 1,2,3-Triazole Nucleosides Based on Functionalized Nicotinonitriles

Faculty Science Year: 2020
Type of Publication: ZU Hosted Pages:
Authors:
Journal: russian journal of organic chemistry Pleiades Publishing, Ltd Volume:
Keywords : Click Synthesis , 1,2,3-Triazole Nucleosides Based , Functionalized Nicotinonitriles    
Abstract:
facile synthesis of a new series of 1,2,3-triazolyl nucleosides via one-pot click reaction is described. Acetylenic nicotinonitriles synthesized previously by alkylation of 4,6-diaryl-2-oxonicotinonitriles with propargyl bromide were involved in cycloaddition with 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl azide in the presence of copper(I) to afford 1,2,3-triazole derivatives which were deprotected by treatment with aqueous triethylamine. The obtained 1,2,3-triazole nucleosides showed significant antimicrobial activities against some Gram-positive and Gram-negative bacteria and fungi.
   
     
 
       

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