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首页> 外文期刊>Journal of Coordination Chemistry >Palladium(II) 9,10-phenanthrenequinone N-substituted thiosemicarbazone/semicarbazone complexes as efficient catalysts for N-arylation of imidazole
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Palladium(II) 9,10-phenanthrenequinone N-substituted thiosemicarbazone/semicarbazone complexes as efficient catalysts for N-arylation of imidazole

机译:9,10-菲醌钯(II)N-取代的硫代半碳//半碳zone配合物是咪唑N-芳基化的有效催化剂

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摘要

A series of palladium complexes, [PdCl(L1-4)] (1-4) (L-1= 9,10-phenanthrenequinone thiosemicarbazone, L-2 = 9,10-phenanthrenequinone methylthiosemicarbazone, L-3 = 9,10-phenanthrenequinone phenylthiosemicarbazone, and L-4 = 9,10-phenanthrenequinone semicarbazone), have been synthesized and characterized by elemental analyses, UV-vis, FT-IR, H-1 and C-13 NMR, and ESI-Mass spectroscopic methods. The catalytic efficiency of the synthesized complexes was examined against N-arylation of imidazole. The system works well with the electron-rich, -neutral, and -deficient aryl halides to afford the products in good to excellent yields. Sterically congested aryl halides and heteroaryl halides have also been used as substrates to provide N-arylated heterocycles. In addition, this methodology can be applicable to other substrates with N-containing heterocycles.
机译:一系列钯配合物[PdCl(L1-4)](1-4)(L-1 = 9,10-菲醌硫代半碳酸钠,L-2 = 9,10-菲醌甲基硫代半碳酰胺,L-3 = 9,10-已通过元素分析,UV-vis,FT-IR,H-1和C-13 NMR以及ESI-Mass光谱法合成并表征了菲醌苯硫半缩酮和L-4 = 9,10菲醌半缩酮。检查了合成配合物对咪唑的N-芳基化反应的催化效率。该系统与富电子,-中性和-不足的芳基卤化物配合良好,从而以良好或优异的收率提供了产物。立体拥挤的芳基卤化物和杂芳基卤化物也已经用作提供N-芳基化杂环的底物。另外,该方法可适用于具有含氮杂环的其他底物。

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