首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Stereoselective synthesis of optically active pyridyl alcohols via asymmetric transfer hydrogenation of pyridyl ketones
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Stereoselective synthesis of optically active pyridyl alcohols via asymmetric transfer hydrogenation of pyridyl ketones

机译:通过吡啶酮的不对称转移氢化立体选择性合成旋光吡啶醇

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摘要

A chiral Ru(II) complex, RuCl[(S,S)-N-(p-toluenesulfonyl)-1,2-diphenyl-ehtylenediamine](p-cyamene), serves as an efficient catalyst for asymmetric transfer hydrogenation of 2-acetylpyridine with a substrate to catalyst molar ratio of 200-1000 with HCOOH as a hydrogen source to give (S)-1-(2-pyridyl)ethanol in an almost quantitative yield and wiht 95% ee.
机译:手性Ru(II)络合物RuCl [(S,S)-N-(对甲苯磺酰基)-1,2-二苯基-乙二胺](对并苯二甲酰基)可作为2-不对称转移加氢的有效催化剂以HCOOH为氢源的底物与催化剂的摩尔比为200-1000的乙酰吡啶,以几乎定量的产率和95%ee得到(S)-1-(2-吡啶基)乙醇。

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