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Efficient synthesis via azide-alkyne Huisgen [3+2] cycloaddition reaction and antifungal activity studies of novel triazoloquinolines

机译:叠氮化物-炔烃Huisgen [3 + 2]环加成反应的高效合成和新型三唑并喹啉类的抗真菌活性研究

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摘要

New functionalized 1,2,3-triazoloquinolines were achieved by intramolecular azide-alkyne Huisgen [3+2] cycloaddition. These derivatives were synthesized via the key Baylis-Hillman adduct under mild, neutral conditions in short duration and consistently good yield. The structures of final compounds were characterized by spectral analysis. Antifungal activities of these analogues against Trichophyton mentagrophytes, Candida albicans, and Aspergillus niger were also assayed.
机译:通过分子内叠氮化物-炔烃Huisgen [3 + 2]环加成反应获得了新的功能化的1,2,3-三唑并喹啉。这些衍生物是通过关键的Baylis-Hillman加合物在温和的中性条件下以较短的持续时间和始终如一的良好收率合成的。最终化合物的结构通过光谱分析表征。还测定了这些类似物对毛癣菌,白色念珠菌和黑曲霉的抗真菌活性。

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