首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis and Antibacterial Activity of New 2,5-Diaryl-3-styryl- 4H,2,3,3a,5,6,6a-hexahydropyrrolo[3,4-d]isoxazole-4,6-diones
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Synthesis and Antibacterial Activity of New 2,5-Diaryl-3-styryl- 4H,2,3,3a,5,6,6a-hexahydropyrrolo[3,4-d]isoxazole-4,6-diones

机译:新型2,5-二芳基-3-苯乙烯基-4H,2,3,3a,5,6,6a-六氢吡咯并[3,4-d]异恶唑-4,6-二酮的合成及抑菌活性

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摘要

The synthesis of some biologically interesting pyrrolo-isoxazolidine derivatives has been accomplished by the 1,3-dipolar cycloaddition reaction of substituted open chain conjugated azomethine N-oxides 1 with substituted N-aryl maleimides 2 leading to the formation of new stereoisomeric 2,5-diaryl-3-styryl- 4H,2,3,3a,5,6,6a-hexahydropyrrolo[3,4-d]isoxazole-4,6-dione derivatives 3 in excellent yields. These stereoisomers have been characterized as cis-3A and trans-3B on the basis of their ~1H-NMR spectral measurements. The synthesized compounds have been screened for their antibacterial activities and have been found to be active against the bacteria Escherichia coli and Pseudomonas aeruginosa up to a significant extent.
机译:某些生物学上有趣的吡咯并异恶唑烷衍生物的合成已通过取代的开链共轭偶氮甲磺酸N-氧化物1与取代的N-芳基马来酰亚胺2的1,3-偶极环加成反应完成,从而导致形成新的立体异构体2,5-二芳基-3-苯乙烯基-4H,2,3,3a,5,6,6a-六氢吡咯并[3,4-d]异恶唑-4,6-二酮衍生物3。这些立体异构体已根据其〜1 H-NMR光谱测量表征为cis-3A和trans-3B。已经对合成的化合物的抗菌活性进行了筛选,并发现它们在很大程度上对大肠杆菌和铜绿假单胞菌具有活性。

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