外消旋化
动力学分辨率
化学
邻接
催化作用
组合化学
对映选择合成
有机化学
分辨率(逻辑)
对映体药物
有机催化
生物催化
化学合成
立体异构
反应条件
作者
Yingqian Jiang,Zhining Li,Shihan Luan,Jiaxuan Li,Chenming Huang,Meiqi Zhao,Xiaodong Wang,Jingxue Zhu,Sizhe Yu,Song You,Bin Y. Qin
标识
DOI:10.1021/acscatal.6c06040
摘要
Abstract Cyclic α-halo ketones and vicinal halohydrins serve as essential synthetic intermediates or structural motifs for a variety of pharmaceuticals. Ketoreductase-catalyzed dynamic reductive kinetic resolution (DYRKR) of cyclic α-halo ketones is an attractive strategy for the synthesis of chiral cyclic vicinal halohydrins. However, we found that the spontaneous racemization of the α-halo groups of 3-bromo-chroman-4-ones and 2-bromo-1-tetralones was less efficient than the ketoreductase-catalyzed reduction of the more reactive enantiomers, resulting in a low conversion and poor (dia)stereoselectivity. To address this challenge, two classes of racemization catalysts were identified: prolinol-derived organocatalysts and racemase-based biocatalysts, both of which could accelerate the racemization of cyclic α-halo ketones. Consequently, combining these catalysts with ketoreductases improved both the conversion and product (dia)stereoselectivity of the DYRKR. Based on the discovery of racemization catalysts, this work provides an efficient strategy for biocatalytic dynamic kinetic resolution and an operationally simple route for the synthesis of chiral cyclic vicinal halohydrins.
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