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Design, synthesis and antifungal activity of novel indole derivatives linked with the 1,2,3-triazole moiety via the CuAAC click reaction

机译:通过CuAAC点击反应与1,2,3-三唑部分连接的新型吲哚衍生物的设计,合成和抗真菌活性

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摘要

A series of novel indole derivatives linked with the 1,2,3-triazole moiety was designed, synthesised by the CuCl2/Zn-catalysed Huisgen cycloaddition and characterised. The antifungal activity of all the prepared compounds against Colletotrichum capsici and cotton Physalospora pathogens was evaluated and the results indicated that these compounds showed inhibitory effect for fungi and the inhibition ratio of the best was up to 83.3%. The preliminary structure-activity relationship is also discussed in this paper.
机译:设计了一系列与1,2,3-三唑部分连接的新型吲哚衍生物,通过CuCl2 / Zn催化的Huisgen环加成反应合成并表征。评价了所制得的全部化合物对辣椒炭疽病和棉衣原体病原菌的抗真菌活性,结果表明这些化合物均对真菌具有抑制作用,最好的抑菌率为83.3%。本文还讨论了初步的构效关系。

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