Synthesis and Antifungal Activity of 4-Aroyl-5-aryl-1-(thymin-5ʹ-yl)triazoles
摘要
Abstract
A library of fifteen triazolyl nucleosides was synthesized by regioselective [3+2] cycloaddition reaction between azido nucleoside and various chalcones under thermal condition in the presence of catalyst tetrabutyl ammonium hydrogen sulfate. All synthesized compounds were evaluated antifungal activity against two phytopathogenic fungi Sclerotium rolfsii and Rhizoctonia solani. Most of the compounds demonstrated good to moderate activity against fungi.