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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Synthesis, characterization and biological studies of some novel 3-fluorosalicylaldehyde based amine derivatives
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Synthesis, characterization and biological studies of some novel 3-fluorosalicylaldehyde based amine derivatives

机译:一些新型的3-氟水杨醛基胺衍生物的合成,表征和生物学研究

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摘要

(Chemical Equation Presented) A series of biologically important substituted 3-fluorosalicylaldehyde derivatives (1a-h) with various primary amines were synthesized by using ionic liquid (1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide) as an efficient catalyst. A new series of Schiff base derivatives (1a-h) were synthesized and characterized by IR, NMR (~1H, ~(13)C, ~1H-~1H COSY and HSQC), mass spectra and elemental analysis. Further crystal structure of compound 1a was evaluated by single crystal X-ray diffraction techniques. All the synthesized compounds were screened for in vitro antimicrobial activity against a panel of selected bacterial and fungal strains using Streptomycin and Amphotericin B as standards. Most of the synthesized compounds demonstrated moderate effects on both antibacterial and antifungal activities at minimum inhibitory concentrations (MIC's).
机译:(提出的化学方程式)通过使用离子液体(1-丁基-3-甲基咪唑双(三氟甲基磺酰基)酰亚胺)作为有效催化剂合成了一系列具有多种伯胺的重要的生物重要的3-氟水杨醛醛衍生物(1a-h)。合成了一系列新的席夫碱衍生物(1a-h),并通过IR,NMR(〜1H,〜(13)C,〜1H-〜1H COZY和HSQC),质谱和元素分析对其进行了表征。化合物1a的进一步晶体结构通过单晶X射线衍射技术评估。使用链霉素和两性霉素B作为标准,针对所有选择的细菌和真菌菌株筛选所有合成的化合物的体外抗菌活性。大多数合成的化合物在最小抑菌浓度(MIC's)下均表现出对抗菌和抗真菌活性的中等作用。

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