首页> 外文期刊>Chemical Communications >Asymmetric construction of trifluoromethylated pyrrolidines via Cu(I)-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with 4,4,4-trifluorocrotonates
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Asymmetric construction of trifluoromethylated pyrrolidines via Cu(I)-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with 4,4,4-trifluorocrotonates

机译:三氟甲基化吡咯烷的不对称结构,通过铜(I)催化偶氮甲亚胺的1,3-偶极环加成反应与4,4,4-三氟巴豆酸酯

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摘要

Trifluoromethylated pyrrolidines have been synthesized via catalytic asymmetric 1,3-dipolar cycloaddition with excellent stereoselectivity for the first time. Epimerization of the endo-pyrrolidines obtained from cis-4,4,4-trifluorocrotonate into the exo-pyrrolidines was also revealed.
机译:三氟甲基化的吡咯烷化合物是通过催化不对称的1,3-偶极环加成反应首次合成的,具有优异的立体选择性。还揭示了从顺式4,4,4-三氟巴豆酸酯获得的内吡咯烷的异构体向外吡咯烷中的异构化。

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  • 来源
    《Chemical Communications》 |2011年第39期|p.11110-11112|共3页
  • 作者单位

    College of Chemistry and Molecular Sciences, Wuhan University,Wuhan 430072, China;

    College of Chemistry and Molecular Sciences, Wuhan University,Wuhan 430072, China;

    College of Chemistry and Molecular Sciences, Wuhan University,Wuhan 430072, China;

    College of Chemistry and Molecular Sciences, Wuhan University,Wuhan 430072, China;

    College of Chemistry and Molecular Sciences, Wuhan University,Wuhan 430072, China,Shanghai Institute of Organic Chemistry, 354 Fenglin Road,Shanghai 200032, China;

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