外消旋化
动力学分辨率
对映体
化学
共价键
对映选择合成
动态共价化学
组合化学
催化作用
基质(水族馆)
手性(物理)
有机化学
超分子化学
分子
海洋学
手征对称破缺
物理
量子力学
夸克
地质学
Nambu–Jona Lasinio模型
作者
Yan Zhang,Yang Zhang,Olof Ramström
标识
DOI:10.1080/01614940.2019.1664031
摘要
Implemented with the highly efficient concept of Dynamic Kinetic Resolution (DKR), dynamic covalent chemistry can be a useful strategy for the synthesis of enantioenriched compounds. This gives rise to dynamic covalent kinetic resolution (DCKR), a subset of DKR that over the last decades has emerged as increasingly fruitful, with many applications in asymmetric synthesis and catalysis. All DKR protocols are composed of two important parts: substrate racemization and asymmetric transformation, which can lead to yields of >50% with good enantiomeric excesses (ee) of the products. In DCKR systems, by utilizing reversible covalent reactions as the racemization strategy, the substrate enantiomers can be easily interconverted without the presence of any racemase or transition metal catalyst. Enzymes or other chiral catalysts can then be adopted for the resolution step, leading to products with high enantiopurities. This tutorial review focuses on the development of DCKR systems, based on different reversible reactions, and their applications in asymmetric synthesis.
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