首页> 外文期刊>The Journal of Organic Chemistry >Tandem C-O and C-N Bonds Formation Through O-Arylation and [3,3]-Rearrangement by Diaryliodonium Salts: Synthesis of N-Aryl Benzo[1,2,3]triazin-4(1H)-one Derivatives
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Tandem C-O and C-N Bonds Formation Through O-Arylation and [3,3]-Rearrangement by Diaryliodonium Salts: Synthesis of N-Aryl Benzo[1,2,3]triazin-4(1H)-one Derivatives

机译:二芳基碘鎓盐通过O-化和[3,3]-重排形成串联C-O和C-N键:N-芳基苯并[1,2,3] triazin-4(1H)-一种衍生物的合成

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摘要

Metal-free O-arylation and [3, 3]-rearrangement have been shown as an efficient strategy to construct new C-O and C-N bonds in one-pot reactions. The method was used to prepare N-aryl benzo[1,2,3]triazin-4(1H)-one derivatives in good yields from N-hydroxy benzo[1,2,3]triazin-4(3H)-one and diaryliodonium salts. The reaction was tolerated a variety of sensitive functional groups such as iodine, nitro, ester, and aldehyde groups. A rational mechanism was proposed based on the experimental results, and the reaction was easily up to gram scale.
机译:无金属的O-芳基化和[3,3]重排已显示为在单反应罐中构建新的C-O和C-N键的有效策略。该方法用于从N-羟基苯并[1,2,3]三嗪-4(3H)-1和N-羟基苯并[1,2,3]三嗪-4(3H)-1制备高收率的N-芳基苯并[1,2,3] triazin-4(1H)-1衍生物。二芳基碘鎓盐。该反应可耐受各种敏感的官能团,例如碘,硝基,酯和醛基。根据实验结果提出了合理的机理,反应容易达到克级。

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