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Transition Metal Nanoparticles on Nano-Level-Controlled Carbon Supports:Efficient Preparative Method of Optically Pure Binaphthyl Derivatives

机译:纳米水平控制碳载体上的过渡金属纳米颗粒:光学纯硼酸二氯基衍生物的高效制备方法

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Enantiomerically pure 1,1'-bi-2-naphthyls such as 1,1'-bi-2-naphthol (BINOL),2,2'-diainino-1,1'-binaphthyl (DABN) and their derivatives (1) are known to be highly useful chiral auxiliaries in the field of asymmetric synthesis.1 The introduction of appropriate substituents at the 3,3'- and/or 6,6'-positions of the original binaphthyl framework (1') is the common method for tuning up their performances.In comparison with such classical modification,recent researches have shown that the chiral catalysts derived from 5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2-naphthyls (Hg-binaphthyls:2) sometimes exhibited higher asymmetric induction than the parent 1,1'-bi-2-naphthyls in many asymmetric reactions.
机译:对映体纯1,1'-Bi-2-萘基,如1,1'-Bi-2-萘酚(Binol),2,2'-二氨基-1,1'-二苯甲基(DABN)及其衍生物(1)已知在非对称合成领域是高度有用的手性助剂.1原始Binaphthyl框架(1')的3,3'-和/或6,6'-位置的适当取代基是常用方法为了调整他们的表演。与这种经典修改的比较,最近的研究表明,衍生自5,5',6,6',7,7',8,8'-octaHydro-1,1'-的手性催化剂Bi-2-萘基(Hg-Binaphthyl:2)有时比许多不对称反应中的母体1,1'-Bi-2-萘基更高的不对称诱导。

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