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首页> 外文期刊>ACS catalysis >Catalytic Desymmetrization of meso-Aziridines with Benzofuran-2(3H)-Ones Employing a Simple In Situ-Generated Magnesium Catalyst
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Catalytic Desymmetrization of meso-Aziridines with Benzofuran-2(3H)-Ones Employing a Simple In Situ-Generated Magnesium Catalyst

机译:使用简单的原位生成镁催化剂的苯并呋喃-2(3H)-催化介孔氮杂环丙烷的不对称化

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摘要

The first example of catalytic desymmetrization of meso-aziridines with benzofuran-2(3H) -ones is realized by employing a magnesium catalyst utilizing BINOL as a simple and commercially available chiral ligand. Both of the enantiomers of the ring-opening product could be easily accessed by employing (R)- or (S)-BINOL as chiral ligand, respectively. A variety of enantioenriched 3,3disubstituted benzofuran-2(3H)-ones containing multiple linear continuous stereocenters were obtained with moderate to good yields, diastereo- and enantioselectivities.
机译:用苯并呋喃-2(3H)-催化内消旋氮丙啶脱甲基化的第一个例子是通过使用利用BINOL作为简单且可商购的手性配体的镁催化剂来实现的。通过分别使用(R)-或(S)-BINOL作为手性配体,可以容易地获得开环产物的两种对映体。获得了具有多个线性连续的立体中心的多种对映体富集的3,3二取代的苯并呋喃-2(3H)-,具有中等至良好的产率,非对映体和对映体选择性。

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