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首页> 外文期刊>Journal of Organometallic Chemistry >Facile synthesis of 5-substituted-1H-tetrazoles and 1-substituted-1H- tetrazoles catalyzed by recyclable 4′-phenyl-2,2′:6′,2″- terpyridine copper(II) complex immobilized onto activated multi-walled carbon nanotubes
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Facile synthesis of 5-substituted-1H-tetrazoles and 1-substituted-1H- tetrazoles catalyzed by recyclable 4′-phenyl-2,2′:6′,2″- terpyridine copper(II) complex immobilized onto activated multi-walled carbon nanotubes

机译:固定在活性多壁碳上的可回收4'-苯基-2,2':6',2''-三联吡啶铜(II)络合物催化的5-取代-1H-四唑和1-取代-1H-四唑的合成纳米管

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摘要

5-Substituted-1H-tetrazoles can conveniently be synthesized from the corresponding nitriles by reaction with NaN_3 using the efficient and recyclable heterogeneous catalyst prepared by immobilization of copper(II) complex of 4′-phenyl-2,2′:6′,2″-terpyridine on activated multi-walled carbon nanotubes [AMWCNTs-O-Cu(II)-PhTPY]. Excellent results were obtained in each case affording the corresponding tetrazole adducts in good to excellent yields. In general, aromatic nitriles with electron-donating group could be accomplished as well as that with electron-withdrawing groups. By leaving out nitrile from the reaction and adding CH(OEt)_3 and amines bearing various substituents, 1-substituted-1H-tetrazoles formed in water in high yields. The reported protocols have the advantages of rapid assembly of a host of heterocyclic systems in high yields with the added advantage of recycling and reuse of the catalyst.
机译:通过使用固定化4'-苯基-2,2':6',2的铜(II)配合物制备的高效可循环使用的非均相催化剂,可以通过与NaN_3反应从相应的腈方便地合成5-取代的1H-四唑活化多壁碳纳米管[AMWCNTs-O-Cu(II)-PhTPY]上的''-叔吡啶。在每种情况下均获得优异的结果,从而以良好至优异的产率提供了相应的四唑加合物。通常,具有给电子基团的芳族腈和具有吸电子基团的芳族腈都可以实现。通过从反应中除去腈并添加CH(OEt)_3和带有各种取代基的胺,可以在水中高产率地形成1-取代-1H-四唑。所报道的方案具有以高收率快速组装大量杂环系统的优点,并具有回收和再利用催化剂的额外优点。

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