首页> 外文期刊>Journal of the American Chemical Society >Direct Boronation of Allyl Alcohols with Diboronic Acid Using Palladium Pincer-Complex Catalysis.A Remarkably Facile Allylic Displacement of the Hydroxy Group under Mild Reaction Conditions
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Direct Boronation of Allyl Alcohols with Diboronic Acid Using Palladium Pincer-Complex Catalysis.A Remarkably Facile Allylic Displacement of the Hydroxy Group under Mild Reaction Conditions

机译:钯钳复合催化直接用二硼酸对烯丙醇进行硼化反应。轻度反应条件下羟基的烯丙基取代反应非常容易

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摘要

Allyl alcohols are one of the most readily available substrates in palladium-catalyzed allylic displacement reactions.Unfortunately,the hydroxy group is one of the most reluctant leaving groups in substitution reactions,and therefore,application of harsh reaction conditions and employment of Lewis acids or other additives are required in these processes.However,employment of these reaction conditions and reagents precludes the efficient synthesis of unstable allyl metal derivatives,such as allyl boronates,in high isolated yields.
机译:烯丙醇是钯催化的烯丙基取代反应中最容易获得的底物之一。不幸的是,羟基是取代反应中最不愿离开的基团之一,因此,在苛刻的反应条件下使用路易斯酸或其他酸在这些过程中需要添加添加剂。但是,由于采用这些反应条件和试剂,以高的分离产率无法有效地合成不稳定的烯丙基金属衍生物,例如硼酸烯丙酯。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2006年第14期|p.4588-4589|共2页
  • 作者单位

    Department of Organic Chemistry,Stockholm University,SE-106 91 Stockholm,Sweden;

    Department of Organic Chemistry,Stockholm University,SE-106 91 Stockholm,Sweden;

    Department of Organic Chemistry,Stockholm University,SE-106 91 Stockholm,Sweden;

    Department of Organic Chemistry,Stockholm University,SE-106 91 Stockholm,Sweden;

  • 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 化学;
  • 关键词

  • 入库时间 2022-08-18 03:22:37

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