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首页> 外文期刊>Advanced synthesis & catalysis >Asymmetric Hydrogenation of beta-Secondary Amino Ketones Catalyzed by a Ruthenocenyl Phosphino-oxazoline-ruthenium Complex (RuPHOX-Ru): the Synthesis of gamma-Secondary Amino Alcohols
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Asymmetric Hydrogenation of beta-Secondary Amino Ketones Catalyzed by a Ruthenocenyl Phosphino-oxazoline-ruthenium Complex (RuPHOX-Ru): the Synthesis of gamma-Secondary Amino Alcohols

机译:钌烯基膦-恶唑啉-钌络合物(RuPHOX-Ru)催化β-仲氨基酮的不对称加氢反应:γ-仲氨基醇的合成

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摘要

A ruthenocenyl phosphino-oxazoline-ruthenium complex (RuPHOX-Ru) was applied successfully to the asymmetric hydrogenation of beta-secondary amino ketones, directly affording the corresponding chiral gamma-secondary amino alcohols in up to 99% yield and with 99% ee. Reaction with beta-(benzylamino)-1-phenylpropan-1-one could be performed on a gram-scale with a relatively low catalyst loading (up to 2000 S/C). The resulting hydrogenated product could be used for the synthesis of synthetically useful compounds.
机译:钌烯基膦基-恶唑啉-钌络合物(RuPHOX-Ru)已成功应用于β-仲氨基酮的不对称氢化反应,直接以高达99%的收率和99%ee的产率提供了相应的手性γ-仲氨基醇。与β-(苄基氨基)-1-苯基丙烷-1-酮的反应可以以克为单位进行,催化剂负载相对较低(最高2000 S / C)。所得的氢化产物可用于合成有用的化合物。

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