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首页> 外文期刊>Organic Chemistry International >Microwave-Assisted Synthesis of Some 1,3,4-Oxadiazole Derivatives and Evaluation of Their Antibacterial and Antifungal Activity
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Microwave-Assisted Synthesis of Some 1,3,4-Oxadiazole Derivatives and Evaluation of Their Antibacterial and Antifungal Activity

机译:微波合成某些1,3,4-恶二唑衍生物及其抗菌和抗真菌活性的评价

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摘要

A series of substituted 1,3,4-oxadiazole derivatives(3a–f)and(6a–f)have been synthesized from diphenylacetic acid hydrazide under microwave irradiation in various reaction conditions. The structures of the synthesized compounds were assigned on the basis of elemental analysis, IR, and1H NMR. These targeted compounds have been tested for their antibacterial and antifungal activities compared to ampicillin and griseofulvin as standard drug. Compounds3a, 3e, 3f, 6c, 6d, 6e, and6dexhibited the maximum antibacterial activities while3b, 3c, 3d, 3e, 6a, 6d, and6eexhibited the maximum antifungal activities.
机译:在微波辐射下,在各种反应条件下,由二苯乙酸酰肼合成了一系列取代的1,3,4-恶二唑衍生物(3a–f)和(6a–f)。合成的化合物的结构是根据元素分析,IR和1 H NMR进行分配的。与氨苄西林和灰黄霉素作为标准药物相比,已经测试了这些靶向化合物的抗菌和抗真菌活性。化合物3a,3e,3f,6c,6d,6e和6具有最大的抗菌活性,而3b,3c,3d,3e,6a,6d和6e具有最大的抗菌活性。

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