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TEMPO-catalyzed synthesis of 5-substituted isoxazoles from propargylic ketones and TMSN3

机译:从丙基酮和TMSN3中催化5-取代异恶唑的合成

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摘要

A novel and efficient TEMPO-catalyzed synthesis of 5-substituted isoxazoles from propargylic ketones and TMSN3 via a radical mechanism process is described. This methodology provides an easy access to a variety of useful 5-substituted isoxazoles from simple and readily available propargylic ketones and TMSN3 in good to excellent yields. A plausible reaction mechanism for this process is proposed.
机译:描述了一种新的和高效的速度催化于来自丙基酮和TMSN3的5-取代异恶唑的合成通过自由基机构方法。 该方法提供了从简单且易于使用的丙基酮和TMSN3的各种有用的5-取代的异恶唑以及优异的产量。 提出了该过程的可粘合反应机制。

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  • 来源
    《RSC Advances》 |2016年第64期|共6页
  • 作者单位

    Guangxi Normal Univ Sch Chem &

    Pharmaceut Sci State Key Lab Chem &

    Mol Engn Med Resources Guilin 541004 Peoples R China;

    Guangxi Normal Univ Sch Chem &

    Pharmaceut Sci State Key Lab Chem &

    Mol Engn Med Resources Guilin 541004 Peoples R China;

    Jishou Univ Coll Chem &

    Chem Engn Jishou 416000 Peoples R China;

    Guangxi Normal Univ Sch Chem &

    Pharmaceut Sci State Key Lab Chem &

    Mol Engn Med Resources Guilin 541004 Peoples R China;

    Guangxi Normal Univ Sch Chem &

    Pharmaceut Sci State Key Lab Chem &

    Mol Engn Med Resources Guilin 541004 Peoples R China;

    Guangxi Normal Univ Sch Chem &

    Pharmaceut Sci State Key Lab Chem &

    Mol Engn Med Resources Guilin 541004 Peoples R China;

    Guangxi Normal Univ Sch Chem &

    Pharmaceut Sci State Key Lab Chem &

    Mol Engn Med Resources Guilin 541004 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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