新型3,4,5-三芳基异恶唑衍生物的高效合成及其抗真菌活性研究

Rajesha Shetty , Syed Shafi , Yuvaraja Kuberan
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引用次数: 1

摘要

以4-溴- 3,5 -二芳基异恶唑为原料,在微波条件下与硼酸进行Suzuki反应,合成了新的3,4,5-三芳基异恶唑衍生物。新合成的化合物通过1H NMR、13C NMR、LC-MS对其结构进行了表征,并对其抗黄曲霉(NCIM No. 524)、尖孢镰镰菌(NCIM No. 1072)和白色念珠菌(NCIM No. 3102)的活性进行了筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficient synthesis of novel 3,4,5-triarylisoxazole derivatives and its antifungal activity studies

Novel 3,4,5-triarylisoxazole derivatives were synthesised by Suzuki reaction of 4-bromo-3, 5-diaryl isoxazoles with various boronic acid under microwave condition. The structures of the newly synthesised compounds are characterised by 1H NMR, 13C NMR, LC-MS and screened for their antifungal activity against Aspergillus flavus (NCIM No. 524), Fusarium oxysporum (NCIM No. 1072) and Candida albicans (NCIM No. 3102).

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