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Neutral iridium catalysts with chiral phosphine-carboxy ligands for asymmetric hydrogenation of unsaturated carboxylic acids

机译:具有手性膦-羧基配体的中性铱催化剂用于不饱和羧酸的不对称加氢

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摘要

We developed neutral iridium catalysts with chiral spiro phosphine-carboxy ligands (SpiroCAP) for asymmetric hydrogenation of unsaturated carboxylic acids. Different from the cationic Crabtree-type catalysts, the iridium catalysts with chiral spiro phosphine-carboxy ligands are neutral and do not require the use of a tetrakis[3,5-bis(trifluoromethyl)phenyl]borate (BArF?) counterion, which is necessary for stabilizing cationic Crabtree-type catalysts. Another advantage of the neutral iridium catalysts is that they have high stability and have a long lifetime in air. The new iridium catalysts with chiral spiro phosphine-carboxy ligands exhibit unprecedented high enantioselectivity (up to 99.4% ee) in the asymmetric hydrogenations of various unsaturated carboxylic acids, particularly for 3-alkyl-3-methylenepropionic acids, which are challenging substrates for other chiral catalysts.
机译:我们开发了具有手性螺膦-羧基配体(SpiroCAP)的中性铱催化剂,用于不饱和羧酸的不对称加氢。与阳离子Crabtree型催化剂不同,具有手性螺膦-羧基配体的铱催化剂是中性的,不需要使用四[3,5-双(三氟甲基)苯基]硼酸酯(BAr F )抗衡离子,这对于稳定阳离子Crabtree型催化剂是必需的。中性铱催化剂的另一个优点是它们具有高稳定性并在空气中具有长寿命。具有手性螺膦-羧基配体的新型铱催化剂在各种不饱和羧酸,特别是3-烷基-3-亚甲基丙酸的不对称加氢中表现出前所未有的高对映选择性(高达99.4%ee),这对其他手性底物而言是具有挑战性的催化剂。

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