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铑催化的苯并二氢吡喃不对称氢芳基化反应中的动力学拆分和动态动力学拆分

Kinetic Resolution and Dynamic Kinetic Resolution of Chromene by Rhodium-Catalyzed Asymmetric Hydroarylation.

作者信息

Yang Qingjing, Wang Yanbo, Luo Shihui, Wang Jun Joelle

机构信息

Department of Chemistry, Southern University of Science and Technology, Shenzhen, Guangdong, 518055, China.

出版信息

Angew Chem Int Ed Engl. 2019 Apr 8;58(16):5343-5347. doi: 10.1002/anie.201900721. Epub 2019 Mar 18.

Abstract

A highly efficient kinetic resolution and dynamic kinetic resolution of chromene is reported for the first time and they procced by a rhodium-catalyzed asymmetric hydroarylation pathway. This new approach offers versatile access to various chiral 2,3-diaryl-chromanes containing vicinal stereogenic centers, as well as the recovered chiral flavenes, in high yields with excellent ee values (s factor up to 532). Particularly noteworthy is that this strategy can be further extended to the establishment of a dynamic version of the kinetic resolution of chromene acetals and allows complete access to chiral isoflavanes and α-aryl hydrocoumarins.

摘要

首次报道了一种高效的色烯动力学拆分和动态动力学拆分方法,该方法通过铑催化的不对称氢芳基化途径进行。这种新方法为以高收率和优异的对映体过量值(s因子高达532)获得各种含有相邻手性中心的手性2,3-二芳基色满以及回收的手性黄酮提供了多种途径。特别值得注意的是,该策略可以进一步扩展到建立色烯缩醛动力学拆分的动态版本,并能够完全获得手性异黄酮和α-芳基氢香豆素。

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