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首页> 外文期刊>New Journal of Chemistry >Facile oxidative cyclization to access C2-quaternary 2-hydroxy-indolin-3-ones: synthetic studies towards matemone
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Facile oxidative cyclization to access C2-quaternary 2-hydroxy-indolin-3-ones: synthetic studies towards matemone

机译:容易氧化环化以获得C2-季 - 羟基 - 吲哚-3-吲哚-3-吲哚 - 吲哚 - 3- in-ins:对Matemone的合成研究

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摘要

A concise and facile approach for the construction of 2-hydroxy-2-substituted indol-3-ones was developed through an oxidative cyclization of 2-aminophenyl-1,3-dione. Using CAN and TEMPO as oxidants, C2-quaternary 2-hydroxy-indolin-3-ones were efficiently installed in moderate to excellent yields (up to 99%). Moreover, this developed protocol was further applied to synthetic studies towards natural product matemone by starting from readily available 2-amino-4-bromobenzoic acid, and the precursor for matemone was efficiently installed.
机译:通过2-氨基苯基-1,3-二酮的氧化环化,通过2-氨基苯基-1,3-二酮构建建造2-羟基-2取代的Indol-3-施工的简洁和容易的方法。 使用CAN和TEMPO作为氧化剂,C2-季铵2-羟基 - 吲哚林-3- 3-吲哚-3-吲哚-3-吲哚-3- inte indegry and ut offerse(高达99%)。 此外,通过从易于使用的2-氨基-4-溴苯甲酸开始,该开发方案进一步应用于天然产物Matemone的合成研究,并且有效地安装了Matemone的前体。

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  • 来源
    《New Journal of Chemistry》 |2017年第20期|共4页
  • 作者单位

    Cent S Univ Coll Chem &

    Chem Engn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Coll Chem &

    Chem Engn Changsha 410083 Hunan Peoples R China;

    Guangxi Teachers Educ Univ Coll Chem &

    Mat Sci Nanning 530001 Guangxi Peoples R China;

    Cent S Univ Coll Chem &

    Chem Engn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Coll Chem &

    Chem Engn Changsha 410083 Hunan Peoples R China;

    Cent S Univ Coll Chem &

    Chem Engn Changsha 410083 Hunan 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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