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ZrCl4-catalyzed C-O bond to C-N bond formation: synthesis of 1,2,3-triazoles and their biological evaluation

机译:ZrCl4催化的C-O键与C-N键的形成:1,2,3-三唑的合成及其生物学评价

摘要

A simple and efficient protocol was developed for the synthesis of aryl azides directly from aryl carbinols using ZrCl4as a Lewis acid catalyst. The azides were converted to novel triazoles under click reaction conditions, which were evaluated for their antimicrobial activity against various strains.
机译:开发了一种简单有效的方案,可使用ZrCl4作为路易斯酸催化剂直接从芳基甲醇合成芳基叠氮化物。在点击反应条件下,将叠氮化物转化为新型三唑,评估其对各种菌株的抗菌活性。

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