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Synthesis of Thiadiazole and Azetidinone Derivatives Derived from Triazoles

机译:三唑衍生的噻二唑和氮杂萘酮衍生物的合成

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摘要

A series of novel thiadiazole and azetidinone derivatives of triazole nucleus were synthesized by the sequence of reactions with conventional and microwave techniques. The microwave technique is very useful with excellent yield at less reaction time compare to other conventional methods. The microwave synthesis of titled compound have been successfully performed in these conditions using environmentally friendly method with high atom economy. These compounds identified and characterized by physical and spectral (IR, NMR) techniques. All the synthesized compounds have been evaluated for their antibacterial and antifungal activity against bacteria Staphylococus aureus and Bacillus subtilis and fungi Fusarium oxisporum and Aspergillus niger when compared with standard drugs.
机译:通过与常规和微波技术的反应序列合成了三唑核的一系列新型噻唑和三唑胺衍生物。 微波技术在与其他常规方法的反应时间较少的反应时间下非常有用。 使用具有高原子经济的环保方法,在这些条件下成功进行了标题化合物的微波合成。 通过物理和光谱(IR,NMR)技术鉴定和表征这些化合物。 已经评估了所有合成的化合物,用于对细菌葡萄球菌和枯草芽孢杆菌和枯草芽孢杆菌和真菌镰刀菌和真菌镰刀菌和真菌患者的抗真菌活性。

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