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A General Solution for Unstable Boronic Acids: Slow-Release Cross-Coupling from Air-Stable MIDA Boronates

机译:不稳定硼酸的一般解决方案:空气稳定的MIDA硼酸盐的缓释交叉偶联

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摘要

Boronic acids can serve as excellent building blocks for the synthesis of a wide range of natural products, Pharmaceuticals, and materials. However, some of the potentially most useful boronic acids, including 2-heterocyclic, vinyl, and cyclopropyl derivatives, are inherently unstable, which can significantly limit their benchtop storage and/or efficient cross-coupling. Many important surrogates have been developed, including trifiuoroborate salts, trialkoxy or trihydroxyborate salts, diethanolamine adducts, sterically bulky boronic esters, and boroxines.
机译:硼酸可以作为合成各种天然产物,药物和材料的出色构建基块。但是,某些潜在最有用的硼酸(包括2-杂环,乙烯基和环丙基衍生物)固有地不稳定,这会极大地限制其台式存储和/或有效的交叉耦合。已经开发出许多重要的替代物,包括三氟硼酸酯盐,三烷氧基或三羟基硼酸酯盐,二乙醇胺加合物,空间体积大的硼酸酯和环硼氧烷。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2009年第20期|6961-6963|共3页
  • 作者单位

    Roger Adams Lab, Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801;

    Roger Adams Lab, Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801;

    Roger Adams Lab, Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801;

  • 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
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