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:立体循环术,动态动力学不对称转化或动态动力学分辨率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已经彻底改变了C-C,C-N和C-X键的方式以对映体纯的形式形成。 特别是将外消旋基质转化为对雌激酶的产物高,理想地定量,产量特别吸引力的不对称反应。 因此,已经开发了许多破坏过程,暗示了概念上不同的策略,例如动态动态的不对称转换(Dykat),动态动态分辨率(DKR)和立体循环术。 在本篇综述中,收集和讨论了外消旋基材的动态金属催化交叉偶联的最新成果,并根据剥离步骤的性质进行讨论。

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