首页> 外文期刊>Organic Chemistry Frontiers >A AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of alpha,beta-unsaturated 7-azaindoline amides and azomethine ylides
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A AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of alpha,beta-unsaturated 7-azaindoline amides and azomethine ylides

机译:前一种/奎宁衍生的氨基磷复合物作为α,β-不饱和7-唑胺酰胺和氮杂甲胺酰胺的α,β-不饱和7-唑胺酰胺的有效催化剂

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摘要

A quinine-derived aminophosphine/ Ag(I) complex was firstly demonstrated to be an efficient catalyst for the highly stereoselective 1,3-dipolar cycloaddition of azomethine ylides with challenging a, beta-unsaturated amide substrates. A wide range of densely functionalized pyrrolidine derivatives containing four contiguous stereogenic centers could be smoothly obtained with excellent diastereo-and enantioselectivities.
机译:首先将奎宁衍生的氨基膦/ Ag(I)复合物作为一种高效的催化剂,用于高度立体选择1,3-偶极环加入的氮杂甲酸钠叶片,具有挑战A,β-不饱和酰胺基材。 含有四种连续立体中心的各种官能化的吡咯烷衍生物可以用优异的非对映异度和对映对激活性平滑地获得。

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  • 来源
    《Organic Chemistry Frontiers》 |2019年第11期|共6页
  • 作者单位

    Chinese Acad Sci Chengdu Inst Organ Chem Natl Engn Res Ctr Chiral Drugs Chengdu 610041 Sichuan Peoples R China;

    Chengdu Univ Inst Adv Study Chengdu 610106 Sichuan Peoples R China;

    Chengdu Univ Inst Adv Study Chengdu 610106 Sichuan Peoples R China;

    Chinese Acad Sci Chengdu Inst Organ Chem Natl Engn Res Ctr Chiral Drugs Chengdu 610041 Sichuan Peoples R China;

    Chinese Acad Sci Chengdu Inst Organ Chem Natl Engn Res Ctr Chiral Drugs Chengdu 610041 Sichuan Peoples R China;

    Chinese Acad Sci Chengdu Inst Organ Chem Natl Engn Res Ctr Chiral Drugs Chengdu 610041 Sichuan Peoples R China;

    Chinese Acad Sci Chengdu Inst Organ Chem Natl Engn Res Ctr Chiral Drugs Chengdu 610041 Sichuan Peoples 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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