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A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones

机译:用于取代(异)喹诺酮类选择性加氢的强力铁催化剂

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摘要

By applying N-doped carbon modified iron-based catalysts, the controlled hydrogenation of N-heteroarenes, especially (iso)quinolones, is achieved. Crucial for activity is the catalyst preparation by pyrolysis of a carbon-impregnated composite, obtained from iron(ii) acetate and N-aryliminopyridines. As demonstrated by TEM, XRD, XPS and Raman spectroscopy, the synthesized material is composed of Fe(0), Fe3C and FeNx in a N-doped carbon matrix. The decent catalytic activity of this robust and easily recyclable Fe-material allowed for the selective hydrogenation of various (iso)quinoline derivatives, even in the presence of reducible functional groups, such as nitriles, halogens, esters and amides. For a proof-of-concept, this nanostructured catalyst was implemented in the multistep synthesis of natural products and pharmaceutical lead compounds as well as modification of photoluminescent materials. As such this methodology constitutes the first heterogeneous iron-catalyzed hydrogenation of substituted (iso)quinolones with synthetic importance.
机译:通过使用N掺杂的碳改性的铁基催化剂,实现了N-杂芳烃,特别是(异)喹诺酮的受控氢化。活性至关重要的是通过热解碳浸渍的复合材料制备催化剂,该复合材料是从乙酸铁(ii)和N-芳基吡啶得到的。如通过TEM,XRD,XPS和拉曼光谱所证明的,合成的材料由N掺杂碳基体中的Fe(0),Fe3C和FeNx组成。这种坚固且易于回收的铁材料具有良好的催化活性,即使在存在可还原的官能团(例如腈,卤素,酯和酰胺)的情况下,也可以选择性氢化各种(异)喹啉衍生物。为了进行概念验证,这种纳米结构催化剂用于天然产物和药物铅化合物的多步合成以及光致发光材料的改性。因此,该方法构成了具有合成重要性的取代的(异)喹诺酮类的第一个多相铁催化的氢化反应。

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