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Manganese complex-catalyzed oxidation and oxidative kinetic resolution of secondary alcohols by hydrogen peroxide

机译:过氧化氢锰络合物催化仲醇的氧化和氧化动力学拆分

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摘要

The highly efficient catalytic oxidation and oxidative kinetic resolution (OKR) of secondary alcohols has been achieved using a synthetic manganese catalyst with low loading and hydrogen peroxide as an environmentally benign oxidant in the presence of a small amount of sulfuric acid as an additive. The product yields were high (up to 93%) for alcohol oxidation and the enantioselectivity was excellent (>90% ee) for the OKR of secondary alcohols. Mechanistic studies revealed that alcohol oxidation occurs via hydrogen atom (H-atom) abstraction from an α-CH bond of the alcohol substrate and a two-electron process by an electrophilic Mn–oxo species. Density functional theory calculations revealed the difference in reaction energy barriers for H-atom abstraction from the α-CH bonds of R- and S-enantiomers by a chiral high-valent manganese–oxo complex, supporting the experimental result from the OKR of secondary alcohols.
机译:在少量硫酸作为添加剂的情况下,使用低载量的合成锰催化剂和过氧化氢作为对环境有益的氧化剂,可以实现仲醇的高效催化氧化和氧化动力学拆分(OKR)。醇氧化的产物收率高(高达93%),仲醇的OKR的对映选择性极好(> 90%ee)。机理研究表明,醇氧化是通过从醇底物的α-CH键中提取氢原子(H原子)和亲电Mn-oxo物种进行的两个电子过程而发生的。密度泛函理论计算揭示了手性高价锰-氧配合物从R-和S-对映体的α-CH键夺取H原子的反应能垒的差异,支持了仲醇OKR的实验结果。

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