首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Stereoselective Metal-Catalyzed C-C Bond Coupling Reactions by Stereoconvergence, Dynamic Kinetic Asymmetric Transformation, or Dynamic Kinetic Resolution
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Stereoselective Metal-Catalyzed C-C Bond Coupling Reactions by Stereoconvergence, Dynamic Kinetic Asymmetric Transformation, or Dynamic Kinetic Resolution

机译:通过立体收敛,动态动力学不对称转变或动态动力学拆分的立体选择性金属催化的C-C键偶联反应

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摘要

The development of stereoselective metal-catalyzed cross-coupling reactions over the past 30 years has revolutionized the way in which C-C, C-N, and C-X bonds are formed in an enantiomerically pure form. In particular asymmetric reactions that transform racemic substrates into enantioenriched products in high, ideally quantitative, yields are particularly appealing. Consequently, many deracemization processes have been developed, implying conceptually diverse strategies such as dynamic kinetic asymmetric transformation (DYKAT), dynamic kinetic resolution (DKR), and stereoconvergence. In this review the most recent achievements in dynamic metal-catalyzed cross couplings of racemic substrates are collected and discussed according to the nature of the deracemization step.
机译:在过去30年中,立体选择性金属催化的交叉偶联反应的发展彻底改变了以对映体纯形式形成C-C,C-N和C-X键的方式。特别是将外消旋底物以理想的定量高收率转化为对映体富集产物的不对称反应特别吸引人。因此,已经开发了许多除轨过程,这暗示了概念上多样化的策略,例如动态动力学非对称变换(DYKAT),动态动力学分辨率(DKR)和立体收敛。在这篇综述中,根据消旋步骤的性质,收集并讨论了外消旋底物在动态金属催化的交叉偶联中的最新成果。

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