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首页> 外文期刊>Tetrahedron >Facile isocyanide-based one-pot three-component regioselective synthesis of highly substituted pyridin-2(1H)-one derivatives at ambient temperature
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Facile isocyanide-based one-pot three-component regioselective synthesis of highly substituted pyridin-2(1H)-one derivatives at ambient temperature

机译:易取代的基于氰化物的一锅三组分区域选择性合成,在环境温度下高度取代的吡啶-2(1H)-一衍生物

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摘要

A novel one-pot three-component regioselective synthesis of highly substituted pyridin-2-one derivatives starting from simple and readily available starting materials is described. The reactive zwitterionic intermediate generated by the addition of an isocyanide to dimethyl acetylenedicarboxylate (DMAD) was trapped with N-arylidene-2-cyanoacetohydrazides to afford the title compounds in moderate to good yields at room temperature without using any catalyst and other additives.
机译:描述了一种从简单易得的起始原料开始的高度取代的吡啶-2-酮衍生物的新颖的一锅三组分区域选择性合成。通过在N-亚芳基-2-氰基乙酰肼中捕获N-亚芳基-2-氰基乙酰肼,将通过向乙炔基二羧酸二甲酯(DMAD)中添加异氰酸酯而生成的反应性两性离子中间体,在不使用任何催化剂和其他添加剂的情况下,以中等至良好的收率得到标题化合物。

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