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首页> 外文期刊>Organic Chemistry Frontiers >Copper-catalyzed radical 1,2-cyclization of indoles with arylsulfonyl hydrazides: access to 2-thiolated 3H-pyrrolo[1,2-a]indoles
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Copper-catalyzed radical 1,2-cyclization of indoles with arylsulfonyl hydrazides: access to 2-thiolated 3H-pyrrolo[1,2-a]indoles

机译:铜催化的基团1,2-环化吲哚芳基肼肼:进入2-硫化的3H- Pyrrolo [1,2-A]吲哚

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摘要

A copper-catalyzed cascade radical 1,2-cyclization of indoles with arylsulfonyl hydrazides was developed, affording a series of 2-thiolated 3H-pyrrolo[1,2-a]indoles in moderate to excellent yields. This transformation proceeded with sequential radical addition to a triple bond and a cyclization procedure, where arylsulfonyl hydrazides served as thioarylation reagents.
机译:开发了一种铜催化的级联1,2-环化吲哚芳基磺基肼的吲哚,得到一系列2-硫化的3H-吡咯[1,2-A]吲哚,中等至优异的产率。 该转化以三键和环化方法进行顺序自由基,其中芳基磺酰基肼用作硫化物试剂。

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  • 来源
    《Organic Chemistry Frontiers》 |2017年第11期|共3页
  • 作者单位

    School of Petrochemical Engineering Jiangsu Key Laboratory of Advanced Catalytic Materials &

    Technology and Institute for Natural and Synthetic Organic Chemistry Changzhou University Changzhou 213164 P. R. China;

    School of Petrochemical Engineering Jiangsu Key Laboratory of Advanced Catalytic Materials &

    Technology and Institute for Natural and Synthetic Organic Chemistry Changzhou University Changzhou 213164 P. R. China;

    School of Petrochemical Engineering Jiangsu Key Laboratory of Advanced Catalytic Materials &

    Technology and Institute for Natural and Synthetic Organic Chemistry Changzhou University Changzhou 213164 P. R. China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
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