首页> 外文期刊>The Journal of Organic Chemistry >Diastereomeric Aziridine Carbinol Catalyzed Enantioselective Arylation Reaction: Toward the Asymmetric Synthesis of Both Enantiomers of Chiral 3?Aryl Phthalide
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Diastereomeric Aziridine Carbinol Catalyzed Enantioselective Arylation Reaction: Toward the Asymmetric Synthesis of Both Enantiomers of Chiral 3?Aryl Phthalide

机译:非对映异构的氮丙啶吡啶甲醇催化的对映选择性的丙烯酸化反应:向手性3?芳基邻苯二酚的两个对映体的不对称合成。

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摘要

The diastereomeric aziridine carbinols are applied, respectively, as efficient chiral ligand in the catalysis of asymmetric arylation and sequential arylation-lactonization cascade. The two diastereomers, which are facilely synthesized from the same chiral source, function as pseudo enantiomers in arylation of aromatic aldehydes providing the different enantiomers of the diarylmethanols with almost the same excellent enantioselectivities. The arylation method is also carried out in tandem with lactonization process to afford a concise synthetic approach to both enantiomers of optically active 3-aryl phthalide.
机译:非对映体氮丙啶甲醇分别用作催化不对称芳基化和顺序芳基化-内酯化级联反应的有效手性配体。这两种非对映异构体是从相同的手性来源中容易合成的,在芳香醛的芳基化反应中用作拟对映异构体,为二芳基甲醇的不同对映异构体提供几乎相同的优异对映选择性。芳基化方法也与内酯化过程一起进行,以为光学活性3-芳基邻苯二甲酸酯的两种对映体提供简明的合成方法。

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