首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Synthesis, characterization, computational calculation and biological studies of some 2,6-diaryl-1-(prop-2-yn-1-yl)piperidin-4-one oxime derivatives
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Synthesis, characterization, computational calculation and biological studies of some 2,6-diaryl-1-(prop-2-yn-1-yl)piperidin-4-one oxime derivatives

机译:某些2,6-二芳基-1-(丙-2-炔-1-基)哌啶-4-酮肟衍生物的合成,表征,计算计算和生物学研究

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A new series of 2,6-diaryl-1-(prop-2-yn-1-yl)piperidin-4-one oximes (17-24) were designed and synthesized from 2,6-diarylpiperidin-4-one oximes (9-16) with propargyl bromide. Unambiguous structural elucidation has been carried out by investigating IR, NMR (H-1, C-13, H-1-H-1 COSY and HSQC), mass spectral techniques and theoretical (DFT) calculations. Further, crystal structure of compound 17 was evaluated by single crystal X-ray diffraction analysis. Single crystal X-ray structural analysis of compound 17 evidenced that the configuration about C=N double bond is syn to C-5 carbon (E-form). The existence of chair conformation was further confirmed by theoretical DFT calculation. All the synthesized compounds were screened for in vitro antimicrobial activity against a panel of selected bacterial and fungal strains using Ciprofloxacin and Ketoconazole as standards. The minimum inhibition concentration (MIC) results revealed that most of the 2,6-diaryl-1-(prop-2-yn-1-yl)piperidin-4-one oximes (17, 19, 20 and 23) exhibited better activity against the selected bacterial and fungal strains. (C) 2014 Elsevier B.V. All rights reserved.
机译:设计并合成了一系列新的2,6-二芳基-1-(丙-2-炔-1-基)哌啶-4-酮肟(17-24),并由2,6-二芳基哌啶-4-酮肟( 9-16)与炔丙基溴。通过研究IR,NMR(H-1,C-13,H-1-H-1 COZY和HSQC),质谱技术和理论计算(DFT)进行了明确的结构解析。此外,通过单晶X射线衍射分析评价化合物17的晶体结构。化合物17的单晶X射线结构分析表明,关于C = N双键的构型与C-5碳同构(E型)。通过理论DFT计算进一步证实了椅子构象的存在。以环丙沙星和酮康唑为标准,对所有合成的化合物针对一组选定的细菌和真菌菌株进行体外抗菌活性筛选。最小抑菌浓度(MIC)结果表明,大多数2,6-二芳基-1-(丙-2-炔-1-基)哌啶-4-酮肟(17、19、20和23)表现出更好的活性针对所选的细菌和真菌菌株。 (C)2014 Elsevier B.V.保留所有权利。

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