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首页> 外文期刊>Organic & biomolecular chemistry >Copper-catalyzed Goldberg-type C-N coupling in deep eutectic solvents (DESs) and water under aerobic conditions
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Copper-catalyzed Goldberg-type C-N coupling in deep eutectic solvents (DESs) and water under aerobic conditions

机译:在有氧条件下深过共晶溶剂(DESS)和水中的铜催化的金牌C-N偶联

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摘要

An efficient and selective N-functionalization of amides is first reported via a Cul-catalyzed Goldberg-type C-N coupling reaction between aryl iodides and primary/secondary amides run either in Deep Eutectic Solvents (DESs) or water as sustainable reaction media, under mild and bench-type reaction conditions (absence of protecting atmosphere). Higher activities were observed in an aqueous medium, though the employment of DESs expanded and improved the scope of the reaction to include also aliphatic amides. Additional valuable features of the reported protocol include: (ⅰ) the possibility to scale up the reaction without any erosion of the yield/reaction time; (ⅱ) the recyclability of both the catalyst and the eutectic solvent up to 4 consecutive runs; and (ⅲ) the feasibility of the proposed catalytic system for the synthesis of biologically active molecules.
机译:首先通过芳基碘化物和初级/二次酰胺之间的CUL催化的Goldberg型CN偶联反应在深海共晶溶剂(DESS)或水中作为可持续反应介质,在轻度和温度下台式反应条件(不存在保护气氛)。在水性介质中观察到更高的活性,尽管DES的就业扩展并改善了反应的范围,但包括脂族酰胺。报告的协议的额外有价值的特征包括:(Ⅰ)可以扩大反应的可能性而不会产生任何侵蚀产量/反应时间; (Ⅱ)催化剂和共晶溶剂的可再循环性最高可连续4次; (Ⅲ)催化系统合成生物活性分子的可行性。

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  • 来源
    《Organic & biomolecular chemistry》 |2021年第8期|1773-1779|共7页
  • 作者单位

    Laboratorio de Compuestos Organometalicos y Catdlisis (Unidad Asociada al CS1C) Departamento de Quimica Orgdnica e Inorgdnica (IUQOEM) Centro de Innovation en Quimica Avanzada (ORFEO-CINQA) Facultad de Quimica Universidad de Oviedo E-33071 Oviedo Spain Dipartimento di Farmacia-Scienze del Farmaco Universita di Ban 'Aldo Moro Consorzio C.I.N.M.P.I.S. Via E. Orabona 4 1-70125 Bari Italy;

    Laboratorio de Compuestos Organometalicos y Catdlisis (Unidad Asociada al CS1C) Departamento de Quimica Orgdnica e Inorgdnica (IUQOEM) Centro de Innovation en Quimica Avanzada (ORFEO-CINQA) Facultad de Quimica Universidad de Oviedo E-33071 Oviedo Spain;

    Dipartimento di Chimica Universita di Bari 'Aldo Moro' Via E. Orabona 4 1-70125 Bari Italy;

    Dipartimento di Farmacia-Scienze del Farmaco Universita di Ban 'Aldo Moro' Consorzio C.I.N.M.P.I.S. Via E. Orabona 4 1-70125 Bari Italy;

    Laboratorio de Compuestos Organometalicos y Catdlisis (Unidad Asociada al CS1C) Departamento de Quimica Orgdnica e Inorgdnica (IUQOEM) Centro de Innovation en Quimica Avanzada (ORFEO-CINQA) Facultad de Quimica Universidad de Oviedo E-33071 Oviedo Spain;

    EntreChem SL Vivero Ciencias de la Salud Santo Domingo de Guzman E-33011 Oviedo Spain;

    Laboratorio de Compuestos Organometalicos y Catdlisis (Unidad Asociada al CS1C) Departamento de Quimica Orgdnica e Inorgdnica (IUQOEM) Centro de Innovation en Quimica Avanzada (ORFEO-CINQA) Facultad de Quimica Universidad de Oviedo E-33071 Oviedo Spain;

    Dipartimento di Farmacia-Scienze del Farmaco Universita di Ban 'Aldo Moro' Consorzio C.I.N.M.P.I.S. Via E. Orabona 4 1-70125 Bari Italy;

    Dipartimento di Farmacia-Scienze del Farmaco Universita di Ban 'Aldo Moro' Consorzio C.I.N.M.P.I.S. Via E. Orabona 4 1-70125 Bari Italy;

    Laboratorio de Compuestos Organometalicos y Catdlisis (Unidad Asociada al CS1C) Departamento de Quimica Orgdnica e Inorgdnica (IUQOEM) Centro de Innovation en Quimica Avanzada (ORFEO-CINQA) Facultad de Quimica Universidad de Oviedo E-33071 Oviedo Spain;

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