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首页> 外文期刊>RSC Advances >Catalytic enantioselective Henry reaction of α-keto esters, 2-acylpyridines and 2-acylpyridine N-oxides
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Catalytic enantioselective Henry reaction of α-keto esters, 2-acylpyridines and 2-acylpyridine N-oxides

机译:α-酮酸酯,2-酰基吡啶和2-酰基吡啶N-氧化物的催化对映选择性亨利反应

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摘要

A pre-prepared Ni–PyBisulidine complex has been developed for the catalytic asymmetric Henry reaction of α-keto esters, 2-acylpyridines and 2-acylpyridine N -oxides. The corresponding β-nitro-α-hydroxy esters were obtained in good to excellent yields (up to 99%) with a high enantiomeric excess (ee) (up to 94%) with a catalyst loading of 1–2 mol%. The desired products of 2-acylpyridines and 2-acylpyridine N -oxides, which were simple methyl ketones, were obtained in medium to excellent yields (up to 94%) with medium to good ee (up to 86%) by using 2 mol% of catalyst.
机译:已经开发了一种预先制备的Ni-PyBisulidine配合物,用于α-酮酸酯,2-酰基吡啶和2-酰基吡啶N-氧化物的催化不对称亨利反应。相应的β-硝基-α-羟基酯以良好至优异的收率(高达99%),高对映体过量(ee)(高达94%)和催化剂负载量为1-2%(摩尔)获得。通过使用2 mol%的中等至良好的ee(高达86%),以中等至优异的收率(高达94%)和中等至良好的ee(高达86%)获得了所需的2-酰基吡啶和2-酰基吡啶N-氧化物(简单的甲基酮)。催化剂。

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