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手性路易斯碱衍生的受阻路易斯酸碱对用于酮和烯酮的不对称氢化反应

Asymmetric Hydrogenation of Ketones and Enones with Chiral Lewis Base Derived Frustrated Lewis Pairs.

作者信息

Gao Bochao, Feng Xiangqing, Meng Wei, Du Haifeng

机构信息

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.

School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Angew Chem Int Ed Engl. 2020 Mar 9;59(11):4498-4504. doi: 10.1002/anie.201914568. Epub 2020 Jan 27.

Abstract

The concept of frustrated Lewis pairs (FLPs) has been widely applied in various research areas, and metal-free hydrogenation undoubtedly belongs to the most significant and successful ones. In the past decade, great efforts have been devoted to the synthesis of chiral boron Lewis acids. In a sharp contrast, chiral Lewis base derived FLPs have rarely been disclosed for the asymmetric hydrogenation. In this work, a novel type of chiral FLP was developed by simple combination of chiral oxazoline Lewis bases with achiral boron Lewis acids, thus providing a promising new direction for the development of chiral FLPs in the future. These chiral FLPs proved to be highly effective for the asymmetric hydrogenation of ketones, enones, and chromones, giving the corresponding products in high yields with up to 95 % ee. Mechanistic studies suggest that the hydrogen transfer to simple ketones likely proceeds in a concerted manner.

摘要

受阻路易斯酸碱对(FLPs)的概念已在各个研究领域中得到广泛应用,无金属氢化无疑是其中最重要且最成功的领域之一。在过去十年中,人们致力于手性硼路易斯酸的合成。与之形成鲜明对比的是,用于不对称氢化的手性路易斯碱衍生的FLPs却鲜有报道。在这项工作中,通过将手性恶唑啉路易斯碱与非手性硼路易斯酸简单组合,开发出了一种新型手性FLP,从而为未来手性FLPs的发展提供了一个有前景的新方向。这些手性FLPs被证明对酮、烯酮和色酮的不对称氢化非常有效,能以高达95%的对映体过量(ee)高产率得到相应产物。机理研究表明,氢向简单酮的转移可能以协同方式进行。

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