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首页> 外文期刊>Journal of the American Chemical Society >Nickel-Catalyzed Asymmetric Reductive Cross-Coupling between Heteroaryl Iodides and α-Chloronitriles
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Nickel-Catalyzed Asymmetric Reductive Cross-Coupling between Heteroaryl Iodides and α-Chloronitriles

机译:杂芳基碘化物和α-氯腈之间镍催化的不对称还原性交叉偶联

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摘要

A Ni-catalyzed asymmetric reductive cross-coupling of heteroaryl iodides and α-chloronitriles has been developed. This method furnishes enantioenriched α,α-disubstituted nitriles from simple organohalide building blocks. The reaction tolerates a variety of heterocyclic coupling partners, including pyridines, pyrimidines, quino-lines, thiophenes, and piperidines. The reaction proceeds under mild conditions at room temperature and precludes the need to pregenerate organometallic nucleophiles.
机译:已开发出Ni催化的杂芳基碘化物和α-氯腈的不对称还原交叉偶联。此方法可从简单的有机卤化物结构单元中提供对映体富集的α,α-二取代的腈。该反应可耐受多种杂环偶联伙伴,包括吡啶,嘧啶,喹啉,噻吩和哌啶。该反应在室温下在温和的条件下进行,因此不需要预先生成有机金属亲核试剂。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2015年第33期|10480-10483|共4页
  • 作者单位

    The Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States;

    The Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, 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
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