首页> 外文期刊>Chemical Communications >Ln[N(SiMe_3)_2]_3-catalyzed cycloaddition of terminal alkynes to azides leading to 1,5-disubstituted 1,2,3-triazoles: new mechanistic features
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Ln[N(SiMe_3)_2]_3-catalyzed cycloaddition of terminal alkynes to azides leading to 1,5-disubstituted 1,2,3-triazoles: new mechanistic features

机译:Ln [N(SiMe_3)_2] _3-催化末端炔烃与叠氮化物的环加成反应,生成1,5-二取代1,2,3-三唑:新的机理

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摘要

The first example of rare earth metal-catalyzed cycloaddition of terminal alkynes to azides resulting in the formation of 1,5-disubstituted 1,2,3-triazoles is described. Preliminary studies revealed that the present cycloaddition shows unprecedented mechanistic features involving a tandem anionic cascade cyclization and anti-addition across the C≡C triple bond.
机译:描述了稀土金属催化的末端炔烃向叠氮化物的环加成反应的第一个例子,该反应导致形成1,5-二取代的1,2,3-三唑。初步研究表明,目前的环加成反应显示出前所未有的机理,包括串联阴离子级联环化反应和跨C≡C三键的反加成反应。

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  • 来源
    《Chemical Communications》 |2013年第49期|5589-5591|共3页
  • 作者单位

    Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China;

    Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, People's Republic of China,State Key Laboratory of Organometallic Chemistry, Shanghai 200032, People's Republic of China;

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  • 入库时间 2022-08-17 13:18:27

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