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Green synthesis of pyrazolo[4,3-d]isoxazol derivatives and their antimicrobial, antimalarial and antituberculosis evaluation

机译:吡唑啉的绿色合成[4,3-D]异恶唑衍生物及其抗微生物,抗疟疾和抗亚伯氏分析

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摘要

This article deals with the synthesis of new pyrazolo[4,3-d]isoxazol derivatives by utilizing 3,4-disubstituted isoxazol-5(4H)-ones and thiosemicarbazide catalyzed by triethylamine in PEG-400 under MWI at 300 W as well as under thermal heating at 90 degrees C. All the synthesized compounds have been characterized by various spectroscopic techniques such as H-1 and C-13 NMR, IR, ESI-MS and elemental analysis. All the synthesized compounds have been screened for antimicrobial, antimalarial and antituberculosis activities.
机译:本文通过利用3,4-二取代的异恶唑-5(4H) - 在MWI下的PEG-400下的三乙胺和300W的PEG-400中的三乙胺催化合成新的吡唑[4,3-D]异恶唑衍生物的合成。 在90℃的热加热下,所有合成的化合物的特征在于各种光谱技术,例如H-1和C-13 NMR,IR,ESI-MS和元素分析。 所有合成的化合物都被筛选用于抗微生物,抗疟疾和抗亚霉菌活动。

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