四配位
阿托品
轴手性
手性(物理)
对映体
动力学分辨率
硼
对映选择合成
立体化学
化学
基质(水族馆)
催化作用
材料科学
计算化学
物理
有机化学
手征对称性
计算机科学
平面的
地质学
计算机图形学(图像)
海洋学
量子力学
Nambu–Jona Lasinio模型
夸克
作者
Kai Yang,Yanfei Mao,Zhihan Zhang,Jie Xu,Hao Wang,He Yong,Peiyuan Yu,Qiuling Song
标识
DOI:10.1038/s41467-023-40164-6
摘要
Catalytic dynamic kinetic asymmetric transformation (DyKAT) provides a powerful tool to access chiral stereoisomers from racemic substrates. Such transformation has been widely employed on the construction of central chirality, however, the application in axial chirality remains underexplored because its equilibrium of substrate enantiomers is limited to five-membered metalacyclic intermediate. Here we report a tetracoordinate boron-directed dynamic kinetic asymmetric cross-coupling of racemic, configurationally stable 3-bromo-2,1-azaborines with boronic acid derivatives. A series of challenging C-B axially chiral compounds were prepared with generally good to excellent enantioselectivities. Moreover, this transformation can also be extended to prepare atropisomers bearing adjacent C-B and C-C diaxes with excellent diastereo- and enantio-control. The key to the success relies on the rational design of a reversible tetracoordinate boron intermediate, which is supported by theoretical calculations that dramatically reduces the rotational barrier of the original C-B axis and achieves the goal of DyKAT.
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