Department of Chemistry, School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Angew Chem Int Ed Engl. 2013 Jun 24;52(26):6590-604. doi: 10.1002/anie.201210066. Epub 2013 May 29.
Catalytic asymmetric carbon-carbon bond-forming reactions provide one of the most efficient ways to synthesize optically active compounds, and, accordingly, many chiral catalysts for these reactions have been developed in the past two decades. However, the efficiency of the catalysts in terms of turnover number (TON) is often lower than that of some other reactions, such as asymmetric hydrogenation, and this has been one of the obstacles for industrial applications. Although there are some difficulties in increasing the efficiency, the issues might be solved by using continuous flow in the presence of chiral heterogeneous catalysts. Indeed, continuous-flow systems have several advantages over conventional batch systems. Here we summarize the recent progress in asymmetric C-C bond-forming reactions under continuous-flow conditions with chiral heterogeneous catalysts.
催化不对称碳-碳键形成反应为合成光学活性化合物提供了最有效的方法之一,因此,在过去的二十年中,已经开发出许多用于这些反应的手性催化剂。然而,催化剂的效率(TON)通常低于其他一些反应,例如不对称氢化,这一直是工业应用的障碍之一。尽管提高效率存在一些困难,但通过在手性多相催化剂存在下使用连续流,这些问题可能会得到解决。事实上,连续流系统相对于传统的间歇系统具有几个优点。在这里,我们总结了在手性多相催化剂存在下连续流条件下不对称 C-C 键形成反应的最新进展。