首页> 外文期刊>Bulletin of the Korean Chemical Society >Enantioselective Hydrogenation of (E)-and (Z)-Isomeric Ethyl 3-Acetamidobutenoates with Rh-Bisphosphine Complexes:Effects of Substrate Geometry and Solvents on Reaction Rates and Catalyst Reusability
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Enantioselective Hydrogenation of (E)-and (Z)-Isomeric Ethyl 3-Acetamidobutenoates with Rh-Bisphosphine Complexes:Effects of Substrate Geometry and Solvents on Reaction Rates and Catalyst Reusability

机译:Rh-双膦配合物对(E)-和(Z)-异美3-乙基乙酰胺基丁烯酸酯的对映选择性加氢:底物几何形状和溶剂对反应速率和催化剂可重用性的影响

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摘要

Enantiopure beta-amino acids are crucial structural features of numerous biologically active natural products as well as important building blocks for the synthesis of beta-peptides and beta-lactam antibiotics.Numbers of stoichiometric chiral auxilaries and catalytic methods have been developed to make chiral beta-amino acids.
机译:对映纯β-氨基酸是许多具有生物活性的天然产物的关键结构特征,也是合成β-肽和β-内酰胺类抗生素的重要基石。已经开发了许多化学计量的手性助剂和催化方法来制备手性β-氨基酸。

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