首页> 外文期刊>Catalysis Letters >Asymmetric Transfer Hydrogenation of Aromatic Ketones Catalyzed by New Chiral C2-Symmetric Bis(sulfonyl) tetraaza Ligands Complexed with [Ru(η~6-p-cymene)Cl2]2 in Water
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Asymmetric Transfer Hydrogenation of Aromatic Ketones Catalyzed by New Chiral C2-Symmetric Bis(sulfonyl) tetraaza Ligands Complexed with [Ru(η~6-p-cymene)Cl2]2 in Water

机译:新型手性C2-对称双(磺酰基)四氮杂配体与[Ru(η〜6-p-cymene)Cl2] 2络合催化芳族酮的不对称加氢

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摘要

In this report, a new series of C2-symmetric bis(sulfonyl) tetraaza ligands were synthesized from (1S,2S)-1,2-diarylethylenediamine analogues and tested in the asymmetric transfer hydrogenation (ATH) of aromatic ketones by complexing with [Ru(η~6-p-cymene)Cl2]2 employing sodium formate as hydrogen source in neat water. A moderate to excellent conversion (~99.8 %) and overall satisfying enantioselectivity (~92.8 %) were obtained with varied electronic and steric effects of the substituents on ligands and substrates.
机译:在此报告中,从(1S,2S)-1,2-二芳基乙二胺类似物合成了一系列新的C2对称双(磺酰基)四氮杂配体,并通过与[Ru]络合在芳香酮的不对称转移氢化(ATH)中进行了测试在纯净水中使用甲酸钠作为氢源的(η〜6-对-cymene)Cl2] 2。在取代基对配体和底物的各种电子和空间效应的影响下,获得了中度至优异的转化率(〜99.8%)和总体令人满意的对映选择性(〜92.8%)。

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