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首页> 外文期刊>Tetrahedron >Mechanistic study on iodine-catalyzed aromatic bromination of aryl ethers by N-Bromosuccinimide
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Mechanistic study on iodine-catalyzed aromatic bromination of aryl ethers by N-Bromosuccinimide

机译:碘催化芳基芳族芳族溴化溴化芳基芳基溴化溴化乙烯的机械研究

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摘要

AbstractAlthough iodine-catalyzed reaction has rapid advances in recent years, examples on iodine-catalyzed bromination are rare and the mechanism of these reactions remains unclear. Herein, we reported an I2-catalyzed aromatic bromination of aryl ethers by NBS and presented the details of the mechanistic study including kinetic study and the study of kinetic isotope effects. The study revealed that the reaction was actually catalyzed by IBr formed in the induction period, and the rate-determining step was the HBr-elimination of the Wheland intermediate assisted by IBr.Graphical abstractDisplay Omitted]]>
机译:<![CDATA [ 抽象 尽管近年来碘催化反应具有快速进展,但碘催化溴化溴化的实例是罕见的和机制这些反应仍然不清楚。在此,我们报道了一种I 2 通过NBS的芳基醚催化芳族溴化溴,并提出了包括动力学研究的机制研究的细节和动力学同位素效应的研究。该研究表明,通过在诱导期间形成的IBR实际上催化反应,速率确定步骤是IBR助康沃兰中间体的HBra-消除。 图形抽象 显示省略 ]]>

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