首页> 外文期刊>Research on Chemical Intermediates >Study of three-component reaction of alpha-ketoesters and active methylenes with OH-acids to synthesize new 2-amino-4H-pyran derivatives and evaluation of their antibacterial and antioxidant activities
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Study of three-component reaction of alpha-ketoesters and active methylenes with OH-acids to synthesize new 2-amino-4H-pyran derivatives and evaluation of their antibacterial and antioxidant activities

机译:用OH-酸的α-酮间酯和活性甲基三组分反应的研究合成新的2-氨基-4H-吡喃衍生物和抗菌和抗氧化活性的评价

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摘要

Synthesis of new derivatives of 2-amino-4H-pyrans is reported via three-component reaction of alpha-ketoesters, active methylenes, and OH-acids in the presence of catalytic amount of piperidine at room temperature with high to excellent yields. The structure of synthesized compounds was characterized by FTIR, H-1, C-13 NMR spectroscopy, and mass spectrometry. Simplicity of procedure, mild reaction conditions, short reaction time, and easy separation of the products make this an interesting alternative to other reported approaches. Also, their antibacterial and antioxidant activities were evaluated against Staphylococcus aureus and Bacillus subtilis as Gram-positive bacteria and Escherichia coli and Pseudomonas aeruginosa as Gram-negative bacteria, as well as the radical scavenger DPPH. Among these compounds, 4l including CO2Et substituent and 6-methyl-2H-pyran-2-one moiety showed the highest antioxidant and antibacterial activities. Graphic abstract
机译:通过α-酮间酯,活性甲基和OH-酸的三分组分反应在室温下在室温下催化量的哌啶的三分组分反应来报告2-氨基-4H-吡喃的新衍生物的合成。 合成化合物的结构的特征在于FTIR,H-1,C-13 NMR光谱和质谱。 手术的简单性,温和的反应条件,短反应时间短,并且易于分离产品使得这是对其他报告的方法的有趣替代品。 此外,它们对葡萄球菌和枯草芽孢杆菌和枯草芽孢杆菌和粒子菌和大肠杆菌和铜绿假单胞菌和铜绿假单胞菌以及自由基清除剂DPPH的抗菌和抗氧化剂活性评估了它们的抗菌和枯草芽孢杆菌。 在这些化合物中,包括CO2ET取代基和6-甲基-2H-吡喃-2-一部分的4L显示出最高的抗氧化剂和抗菌活性。 图形摘要

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