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首页> 外文期刊>Journal of the American Chemical Society >P~Ⅲ/P~Ⅴ=O-Catalyzed Intermolecular N-N Bond Formation: Cross-Selective Reductive Coupling of Nitroarenes and Anilines
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P~Ⅲ/P~Ⅴ=O-Catalyzed Intermolecular N-N Bond Formation: Cross-Selective Reductive Coupling of Nitroarenes and Anilines

机译:P〜Ⅲ/ p〜= o催化分子间N-N键形成:硝基拉酮和苯胺的交叉选择性还原偶联

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摘要

An organophosphorus-catalyzed method for the synthesis of unsymmetrical hydrazines by cross-selective intermolecular N-N reductive coupling is reported. This method employs a small ring phosphacycle (phosphetane) catalyst together with hydrosilane as the terminal reductant to drive reductive coupling of nitroarenes and anilines with good chemoselectivity and functional group tolerance. Mechanistic investigations support an autotandem catalytic reaction cascade in which the organophosphorus catalyst drives two sequential and mechanistically distinct reduction events via P~Ⅲ/P~Ⅴ=O cycling in order to furnish the target N-N bond.
机译:报道了通过交叉选择性分子间N-N还原偶联来合成非对称肼的有机磷催化方法。 该方法采用小环磷酸盐(磷酸乙烷)催化剂与氢硅烷一起作为末端还原剂,以驱动硝基甲烷和苯胺的还原偶联,具有良好的化学选择性和官能团耐受性。 机械研究支持自同磷催化反应级联,其中有机磷催化剂通过P〜Ⅲ/ p〜= =循环驱动两个顺序和机械上不同的减少事件,以便提供靶N-N键。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2021年第36期|14464-14469|共6页
  • 作者单位

    Department of Chemistry Massachusetts Institute of Technology Cambridge Massachusetts 02139 United States;

    Department of Process Research and Development Merck & Co. Inc. West Point Pennsylvania 19486 United States;

    Department of Chemistry Massachusetts Institute of Technology Cambridge Massachusetts 02139 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);
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  • 正文语种 eng
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