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Mechanism of Cu-Catalyzed Aryl Boronic Acid Halodeboronation Using Electrophilic Halogen: Development of a Base-Catalyzed lododeboronation for Radiolabeling Applications

机译:用电泳卤素的Cu催化芳基硼酸卤代酸卤钨的机理:碱催化洛氏卵德萎缩用于放射性标记应用的影响

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摘要

An investigation into the mechanism of Cu-catalyzed aryl boronic acid halodeboronation using electrophilic halogen reagents is reported. Evidence is provided to show that this takes place via a boronate-driven ipso-substitution pathway and that Cu is not required for these processes to operate: general Lewis base catalysis is operational. This in turn allows the rational development of a general, simple, and effective base-catalyzed halodeboronation that is amenable to the preparation of I-125-labeled products for SPECT applications.
机译:据报道了使用亲电卤素试剂的Cu催化芳基硼酸卤霉硼酸盐机理的研究。 提供证据表明,这是通过硼酸盐驱动的IPSO替代途径进行,并且这些过程操作不需要CU:通用刘易斯催化是运作的。 这反过来允许理性的碱基催化卤代硼酸的理性开发,其适用于制备用于SPECT应用的I-125标记的产品。

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  • 来源
    《Organic letters》 |2019年第7期|共5页
  • 作者单位

    Univ St Andrews Sch Chem EaStCHEM St Andrews KY16 9ST Fife Scotland;

    Univ Glasgow Sch Chem WestCHEM Joseph Black Bldg Univ Ave Glasgow G12 8QQ Lanark Scotland;

    Univ Strathclyde Dept Pure &

    Appl Chem WestCHEM 295 Cathedral St Glasgow G1 1XL Lanark Scotland;

    Univ Glasgow Sch Chem WestCHEM Joseph Black Bldg Univ Ave Glasgow G12 8QQ Lanark Scotland;

    Univ St Andrews Sch Chem EaStCHEM St Andrews KY16 9ST Fife Scotland;

    Greater Glasgow &

    Clyde NHS Trust West Scotland PET Ctr Glasgow G12 0YN Lanark Scotland;

    Univ Glasgow Sch Chem WestCHEM Joseph Black Bldg Univ Ave Glasgow G12 8QQ Lanark Scotland;

    Univ St Andrews Sch Chem EaStCHEM St Andrews KY16 9ST Fife Scotland;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

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