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首页> 外文期刊>Chirality: The pharmacological, biological, and chemical consequences of molecular asymmetry >Chiral Amino Amides for the Ruthenium(II)-Catalyzed Asymmetric Transfer Hydrogenation Reaction of Ketones in Water
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Chiral Amino Amides for the Ruthenium(II)-Catalyzed Asymmetric Transfer Hydrogenation Reaction of Ketones in Water

机译:手性氨基酰胺用于钌(II)催化的酮在水中的不对称转移加氢反应

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摘要

The chiral amino amide 3 was derived from L-proline and used for the [RuCl2(p-cymene)](2)-catalyzed asymmetric transfer hydrogenation of prochiral ketones performed in water. Moderate to good chemical selectivities (up to 95% yield) mid enantioselectivities (up to 90% ee) were obtained in the presence of 2 mol % of TBAB (n-Bu4NBr) as the phase transfer catalyst.
机译:手性氨基酰胺3衍生自L-脯氨酸,用于[RuCl2(p-cymene)](2)催化的前手性酮在水中的不对称转移氢化。在存在2mol%的TBAB(n-Bu4NBr)作为相转移催化剂的情况下,获得了中等至良好的化学选择性(最高95%的收率),中等对映选择性(最高90%ee)。

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