A novel and efficient synthe'/> Alkali-Induced Ring-Opening of 2-Amidodihydrofuran and Manganese-Catalyzed Aerobic Dehydrogenation Annulation: Access?to Functionalized Oxazole
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Alkali-Induced Ring-Opening of 2-Amidodihydrofuran and Manganese-Catalyzed Aerobic Dehydrogenation Annulation: Access?to Functionalized Oxazole

机译:碱诱导的2- amidodihydrofuran和锰催化的有氧脱氢环测量的开环:进入?到官能化的恶唑

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src="http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/joceah/2017/joceah.2017.82.issue-9/acs.joc.7b00112/20170501/images/medium/jo-2017-00112d_0011.gif">A novel and efficient synthesis of functionalized oxazoles from 2-amidodihydrofurans has been achieved by alkali-induced intramolecular C–O bond cleavage and formation using air as a green oxidant. Moreover, these functionalized oxazoles could be readily transformed into the corresponding oxazole-substituted pyrazoles and 2H-azirines.
机译:src =“http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/joceah/2017/joceah.2017.82.issue-9/acs.joc.7b00112/2017050501/images/medium / jo-2017-00112d_0011.gif“>通过碱诱导的分子内C-O键粘合和使用空气作为绿色氧化剂,通过碱诱导的分子内C-O键粘合和形成来实现从2-脒二呋喃呋喃的新颖和有效合成官能化的恶唑。 此外,这些官能化的恶唑可以容易地转化到相应的氧唑取代的吡唑和2℃-H / I> -Adirines中。

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  • 来源
    《The Journal of Organic Chemistry》 |2017年第9期|共9页
  • 作者单位

    State Key Laboratory for Oxo Synthesis and Selective Oxidation Lanzhou Institute of Chemical Physics Chinese Academy of Sciences Lanzhou 730000 P. R. China;

    State Key Laboratory for Oxo Synthesis and Selective Oxidation Lanzhou Institute of Chemical Physics Chinese Academy of Sciences Lanzhou 730000 P. R. China;

    State Key Laboratory for Oxo Synthesis and Selective Oxidation Lanzhou Institute of Chemical Physics Chinese Academy of Sciences Lanzhou 730000 P. R. China;

    State Key Laboratory for Oxo Synthesis and Selective Oxidation Lanzhou Institute of Chemical Physics Chinese Academy of Sciences Lanzhou 730000 P. R. China;

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  • 正文语种 eng
  • 中图分类 有机化学;
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