首页> 外文会议>Symposium on Organometallic Chemistry >Synthesis of Substituted 2,2'-Bipyridines by Cobalt-Catalyzed Cycloaddition Reactions of Nitriles and 1,6-Diynes with Exclusive Regioselectivity
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Synthesis of Substituted 2,2'-Bipyridines by Cobalt-Catalyzed Cycloaddition Reactions of Nitriles and 1,6-Diynes with Exclusive Regioselectivity

机译:用腈钴催化的环加成反应合成腈和1,6-迪杨的钴催化的循环加油反应

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2,2'-bipyridines are of great importance as the substructure of biologically active compounds and particularly as a ligand capable of attaching to various metal atoms and,therefore,development of their synthesis is desired.We have recently developed a facile formation of substituted pyridines by [2 + 2 + 2] cycloaddition reaction of alpha,omega-diynes and nitriles by using a 1,2-bis(diphenylphosphino)ethane (dppe)/CoCl,-6H2O/Zn catalyst,where unactivated nitiles such as acetonitrile and benzonitrile reacted smoothly under mild reaction conditions.
机译:2,2'-Bi0 yridines作为生物活性化合物的亚结构,特别是作为能够连接到各种金属原子的配体,因此期望它们的合成的发展。我们最近开发了替代吡啶的容易形成通过使用1,2-双(二苯基膦基)乙烷(DPPE)/ COCl,-6H2O / Zn催化剂,α,Omega-Diyγ和腈的环加成反应,其中甲烷(DPPE)/ COCl,-6H2O / Zn催化剂,其中未激活的纽瓦尔,如乙腈和苯腈在轻度反应条件下平滑地反应。

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