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An Efficient Process for Pd-Catalyzed C-N Cross-Coupling Reactions of Aryl Iodides: Insight Into Controlling Factors

机译:Pd催化芳基碘化物的C-N交叉偶联反应的有效过程:对控制因素的认识

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摘要

In Pd-catalyzed C-C cross-coupling reactions aryl iodides have generally been better substrates than the corresponding aryl bromides or chlorides. However, this has not been the case for Pd-catalyzed C-N bond-forming processes, in which aryl iodides have traditionally been the least successful substrates of these three aryl halides. Recent advances in this field have allowed for reactions of aryl chlorides to reach the same efficiencies as aryl bromides, but relatively little progress has been made in increasing the proficiency of Pd-catalyzed C-N cross-coupling processes using aryl iodides.
机译:在钯催化的C-C交叉偶联反应中,芳基碘化物通常是比相应的芳基溴化物或氯化物更好的底物。但是,Pd催化的C-N键形成过程并非如此,传统上,芳基碘化物是这三种芳基卤化物中最不成功的底物。该领域的最新进展已使芳基氯化物的反应达到与芳基溴化物相同的效率,但是在提高使用芳基碘化物的Pd催化的C-N交叉偶联效率方面取得的进展相对较少。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2009年第16期|5766-5768|共3页
  • 作者单位

    Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139;

    Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139;

    Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139;

  • 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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