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Chiral Synthesis of McGeachin-Type Bisaminals

机译:手性合成McGeachin-型Bisaminals

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摘要

Bridged [3.3.1]-bisaminal structures, namely 6,12-epiminodibenzo[bf][1,5]diazocines, are herein named McGeachin-type bisaminals. The TsOH-catalyzed chiral synthesis of McGeachin-type bisaminals is first developed by condensation of two molecules of 2-(methylamino)benzaldehyde and one molecule of chiral amines. Two chiral diastereomers are generated simultaneously and are isolated by column chromatography in a total yield of up to 99%. The absolute structure of one stereoisomer was determined by X-ray crystallography.
机译:桥接[3.3.1] - 水分结构,即6,12-Epiminodibenzo [BF]重氮化,本文称为McGeachin-型Bisaminals。 首先通过2-(甲基氨基)苯甲醛和一种手性胺的分子缩合,首先开发TSOH催化的手性合成麦克顿型Bisaminals。 同时产生两种手性非对映异构体,并通过柱色谱分离,其总收率高达99%。 通过X射线晶体学确定一个立体异构体的绝对结构。

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  • 来源
    《The Journal of Organic Chemistry》 |2020年第5期|共8页
  • 作者单位

    Beijing Univ Chem Technol Dept Organ Chem Coll Chem State Key Lab Chem Resource Engn Beijing 100029 Peoples R China;

    Beijing Univ Chem Technol Dept Organ Chem Coll Chem State Key Lab Chem Resource Engn Beijing 100029 Peoples R China;

    Guilin Univ Technol Coll Chem &

    Bioengn Guangxi Key Lab Electrochem &

    Magnetochem Funct M Guilin 541004 Guangxi Peoples R China;

    Beijing Univ Chem Technol Dept Organ Chem Coll Chem State Key Lab Chem Resource Engn Beijing 100029 Peoples R China;

    Beijing Univ Chem Technol Dept Organ Chem Coll Chem State Key Lab Chem Resource Engn Beijing 100029 Peoples R China;

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  • 正文语种 eng
  • 中图分类 有机化学;
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