使用分子碘作为合成苯并咪唑衍生物的唯一氧化剂,已经实现了分子内芳基CH氨基化反应。通过将芳基胺与相应的腈或芳基碘加成或偶联,可以轻松制备所需的底物。在以碳酸钾(K 2 CO 3)为碱的情况下,这些底物的碘介导的氧化环化作用可提供中等至良好收率的相应产物。此处介绍的无过渡金属协议对空气不敏感,操作简单。这种通用且环保的合成方法学广泛适用于各种N芳基取代的am和吡啶2胺,可直接接触1 H来自相应前体的-苯并[ d ]咪唑和吡啶并[1,2- a ]苯并咪唑衍生物。
Facile Synthesis of Amidines via the Intermolecular Reductive Coupling of Nitriles with Nitro Compounds Induced by Samarium(ii) Iodide
作者:Longhu Zhou、Yongmin Zhang
DOI:10.1039/a803011a
日期:——
The intermolecular reductive coupling of nitriles with nitro compounds induced by SmI2 was studied; amidine derivatives are prepared in good yields under neutral and mild conditions.
Low-Valent Titanium Induced Reductive Coupling of Nitriles with Nitro Compounds
作者:Longhu Zhou、Yongmin Zhang
DOI:10.1080/00397919808004430
日期:1998.9
Abstract The intermolecular and intramolecular reductivecoupling of a cyano group with a nitro group induced by a low-valenttitanium reagent prepared from TiCl4/Sm was studied. Amidines and 2-aminoquinolines derivatives are preparied in good yields under mild conditions respectively.