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首页> 外文期刊>Chemistry Letters >Synthesis of P-Stereogenic Phosphinates via an Axis-to-Center Chirality Transfer by the Reaction of Phosphonates Having a Binaphthyloxy Group with Grignard Reagents
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Synthesis of P-Stereogenic Phosphinates via an Axis-to-Center Chirality Transfer by the Reaction of Phosphonates Having a Binaphthyloxy Group with Grignard Reagents

机译:通过用格氏试剂的膦酸膦酸盐反应来合成通过轴向中心的螯合剂通过磷酸膦酸盐的反应来转移

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摘要

The reactions of phosphonates having a binaphthyloxy group with Grignard reagents gave the corresponding P-stereogenic phosphinates in good to high yields with high diastereoselectivity. In this reaction, an axis-to-center chirality transfer from a binaphthyl group to the resulting phosphorus atom took place stereospecifically. Both diastereomers with opposite configurations could be obtained by changing the combination of carbon-containing functional groups on the phosphorus atom and the Grignard reagents.
机译:具有GRIGNARD试剂的膦酸膦酸膦酸膦酸酯的反应使相应的P-立体膦酸含量良好地具有高屈服度的高产率。 在该反应中,从二萘基到所得磷原子的轴向中心肾上腺素发生,发生立体化。 通过改变磷原子和格氏试剂上的含碳官能团的组合可以获得具有相反构型的非对映异构体。

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