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首页> 外文期刊>Organic letters >Facile Development of Chiral Alkenylboranes from Chiral Diynes for Asymmetric Hydrogenation of Silyl Enol Ethers
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Facile Development of Chiral Alkenylboranes from Chiral Diynes for Asymmetric Hydrogenation of Silyl Enol Ethers

机译:从手性二炔中手性烯基硼烷的不对称氢化硅烯醇醚的轻松开发

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摘要

A facile development of chiral alkenylboranes by the hydroboration of chiral diynes with Piers borane was successfully achieved for the first time. With the combination of the in situ generated chiral alkenylboranes and tri-tert-butylphosphine as frustrated Lewis pair catalysts, the metal-free asymmetric hydrogenation of silyl enol ethers was realized to furnish a wide range of optically active secondary alcohols in high yields and up to 99% ee.
机译:首次成功地通过手性二炔与Piers硼烷的硼氢化反应轻松开发了手性烯基硼烷。通过原位生成的手性链烯基硼烷和三叔丁基膦作为受阻的路易斯对催化剂的组合,实现了甲硅烷基烯醇醚的无金属不对称加氢,从而以高收率提供了多种旋光性仲醇。 99%ee。

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