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Palladium(Ⅲ)-Catalyzed Fluorination of Arylboronic Acid Derivatives

机译:钯(Ⅲ)催化芳基硼酸衍生物的氟化

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摘要

A practical, palladium-catalyzed synthesis of aryl fluorides from arylboronic acid derivatives is presented. The reaction is operationally simple and amenable to multigram-scale synthesis. Evaluation of the reaction mechanism suggests a single-electron-transfer pathway, involving a Pd(Ⅲ) intermediate that has been isolated and characterized.
机译:提出了由芳基硼酸衍生物实际,钯催化的芳基氟化物的合成。该反应操作简单并且适合于多克级合成。对反应机理的评估表明,该单电子转移途径涉及已分离和表征的Pd(Ⅲ)中间体。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2013年第38期|14012-14015|共4页
  • 作者单位

    Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, United States;

    Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, United States;

    Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, United States;

    Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, United States;

    Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 03:12:51

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