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Water-Promoted Heterogeneous Asymmetric Hydrogenation of Quinolines over Ordered Macroporous Poly(ionic liquid) Catalyst

机译:在有序大孔聚(离子液体)催化剂上喹啉的水促进的异质不对称氢化

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摘要

The development of air stable solid chiral catalysts for asymmetric hydrogenation is very attractive for the large-scale production of chiral compounds. Herein, we reported the synthesis of an ordered macroporous poly(ionic liquid) catalyst integrated with VDPEN-RuOTf as air stable chiral catalyst for asymmetric hydrogenation of quinoline derivatives. Under ambient conditions, the solid catalyst afforded 97% conversion with 90% ee in the asymmetric hydrogenation of 2-methylquinoline in water. It was found that the activity and enantioselectivity of poly(ionic liquid) catalyst decreases with surface hydrophobicity increasing, suggesting the important role of surface hydrophilicity in obtaining high activity and enantioselectivity in water. Control experiment suggests that water promotes the anti-air stability of the poly(ionic liquid) catalyst. The combination of poly(ionic liquid) catalyst and water may provide a new approach for designing heterogeneous chiral catalyst with anti-air stability.
机译:对于不对称氢化的空气稳定固体手性催化剂的开发对于对手性化合物的大规模产生非常有吸引力。在此,我们报道了与VDPEN-Ruotf相结合的有序大孔聚(离子液体)催化剂的合成,作为喹啉衍生物的不对称氢化的空气稳定的手性催化剂。在环境条件下,固体催化剂在水中2-甲基喹啉的不对称氢化中得到97%的转化率。发现聚(离子液体)催化剂的活性和对辅助性与表面疏水性增加降低,表明表面亲水性在水中获得高活性和对映选择性的重要作用。对照实验表明水促进了聚(离子液体)催化剂的抗空气稳定性。聚(离子液体)催化剂和水的组合可以提供一种具有抗空气稳定性的非均相手性催化剂的新方法。

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