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Microwave Assisted Synthesis of Some New Heterocyclic Spiro-Derivatives with Potential Antimicrobial and Antioxidant Activity

机译:微波辅助合成某些具有潜在抗微生物和抗氧化活性的杂环螺衍生物

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摘要

Homophthalic anhydride reacts with different aromatic amines to produce N-substituted homophthalimides. Bromination of the latter produces 4,4-dibromo-homophthalimide derivatives that can be used as precursors for spiro-derivatives. The dibromo derivatives react with different binucleophilic reagents to produce several spiro-isoquinoline derivatives. Reaction of the dibromo derivatives with malononitrile produces dicyanomethylene derivatives which react with different binucleophiles to produce new spiro-derivatives. Structures of the newly synthesized compounds are proved using spectroscopic methods such as IR, 1H-NMR and 13C-NMR. The newly synthesized compounds were tested for their antimicrobial and antioxidant activities, showing weak or no antimicrobial activity. On the other hand select compounds showed promising antioxidant activities.
机译:高邻苯二甲酸酐与不同的芳族胺反应生成N-取代的高邻苯二甲酰亚胺。后者的溴化反应可生成4,4-二溴-邻苯二甲酰亚胺衍生物,可用作螺旋衍生物的前体。二溴衍生物与不同的双亲核试剂反应生成几种螺-异喹啉衍生物。二溴衍生物与丙二腈的反应产生二氰基亚甲基衍生物,其与不同的双亲核试剂反应以产生新的螺环衍生物。用红外光谱, 1 H-NMR和 13 C-NMR等分光光度法证明了新合成化合物的结构。测试了新合成的化合物的抗微生物和抗氧化活性,显示弱或无抗微生物活性。另一方面,选择的化合物显示出有希望的抗氧化剂活性。

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