1,2,3-三唑类抗真菌化合物的设计与合成

Erick Cuevas Yañez
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引用次数: 2

摘要

1,2,3-三氮唑是一种很容易由CuAAC反应制备的抗真菌化合物,是一种类似于唑类药物的潜在来源。因此,研究小组通过叠氮或炔前体中的取代基合成了多种具有调节抗真菌活性的1,2,3-三唑。简要回顾了有关这一主题的最新进展,重点介绍了开发新的和更具选择性的抗真菌化合物的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design and Synthesis of Antifungal Compounds from 1,2,3-Triazoles through the Click Chemistry Approach
1,2,3-triazoles are easily prepared from CuAAC reaction and represent a potential source of antifungal compounds analogous to azole drugs. Accordingly, research groups have synthesized diverse 1,2,3-triazoles with modulated antifungal activity through the substituents in azide or alkyne precursors. A brief review of the state of the art about this topic is presented, focusing the increasing importance of developing new and more selective antifungal compounds.
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