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Iodine-mediated C–N and N–N bond formation: a facile one-pot synthetic approach to 1,2,3-triazoles under metal-free and azide-free conditions

机译:碘介导的C–N和N–N键的形成:一种在无金属和无叠氮条件下简便地一锅合成1,2,3-三唑的方法

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A novel strategy towards the synthesis of 1,4-disubstituted 1,2,3-triazoles via C–N and N–N bond formation has been demonstrated under transition metal-free and azide-free conditions. These 1,2,3-triazoles were obtained in a regioselective manner from commercially available anilines, aryl alkenes/aryl alkynes and N -tosylhydrazines using I _(2) under O _(2) atmosphere. Broad substrate scope, milder reaction conditions, good to moderate yields and clean protocol are the notable features of the method. Moreover, this protocol is amenable for the generation of a library of medicinally important key building blocks.
机译:在无过渡金属和无叠氮化物的条件下,已经证明了通过C–N和N–N键的形成合成1,4-二取代1,2,3-三唑的一种新策略。这些1,2,3-三唑以区域选择性的方式在I_(2)气氛下使用I_(2)从市售苯胺,芳基烯烃/芳基炔烃和N-甲苯磺酰基肼获得。该方法的显着特点是底物范围广,反应条件温和,收率中等至中等,操作规程纯正。此外,该协议适用于生成医学上重要的重要构建模块库。

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