首页> 外文期刊>Advanced synthesis & catalysis >Axial Chirality Control by 2,4-Pentanediol for the Alternative Synthesis of C_3*-TunePhos Chiral Diphosphine Ligands and Their Applications in Highly Enantioselective Ruthenium-Catalyzed Hydrogenation of β-Keto Esters
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Axial Chirality Control by 2,4-Pentanediol for the Alternative Synthesis of C_3*-TunePhos Chiral Diphosphine Ligands and Their Applications in Highly Enantioselective Ruthenium-Catalyzed Hydrogenation of β-Keto Esters

机译:2,4-戊二醇的轴向手性控制对C_3 * -TunePhos手性二膦配体的交替合成及其在高对映选择性钌催化的β-酮基酯加氢中的应用

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摘要

A highly efficient strategy for the synthesis of a series of C3*-TunePhos chiral diphosphine ligands was well established with several remarkable features. The synthetic utility of these ligands was explored for the ruthenium-catalyzed asymmetric hydrogenation of β-keto esters. Up to 99% ee values were achieved for the enantioselective synthesis of β-hydroxy acid derivatives, which are very important chiral building blocks for the synthesis of a variety of natural products and biologically active molecules.
机译:具有多种显着特征的合成一系列C3 * -TunePhos手性二膦配体的高效策略已得到良好确立。探索了这些配体的合成效用,用于钌催化的β-酮酯的不对称氢化。 β-羟酸衍生物的对映选择性合成获得了高达99%的ee值,这是合成多种天然产物和生物活性分子的非常重要的手性构建基。

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