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手性 N-杂环卡宾配体在不对称过渡金属催化中的优势。

Privileged chiral N-heterocyclic carbene ligands for asymmetric transition-metal catalysis.

机构信息

Westfälische Wilhelms-Universität Münster, Organisch-Chemisches Institut, Corrensstrasse 40, 48149 Münster, Germany.

出版信息

Chem Soc Rev. 2017 Aug 14;46(16):4845-4854. doi: 10.1039/c7cs00200a.

Abstract

Chiral ligands play a central role in enantioselective transition-metal catalysis. The success of achiral N-heterocyclic carbenes (NHCs) as stable electron-rich neutral ligands in homogeneous catalysis led to the development of a manifold of chiral NHCs as stereodirecting ancillary ligands for various enantioselective transformations. Due to the modular design of NHCs and the ease of access to their azolium salt precursors, tailor-made NHCs are readily available. Many chiral NHC scaffolds have been synthesised and tested in catalysis. Herein, we highlight only those NHC structures which have enabled high degrees of enantioselectivity in transition-metal catalysis. Following a brief introduction to the field of chiral NHCs, this tutorial review introduces different categories of chiral NHCs and provides a guide to the structural fine-tuning of ligand requirements and stereochemical models.

摘要

手性配体在对映选择性过渡金属催化中起着核心作用。非手性 N-杂环卡宾 (NHC) 作为均相催化中稳定的富电子中性配体的成功,导致了多种手性 NHC 的发展,作为各种对映选择性转化的立体定向辅助配体。由于 NHC 的模块化设计和易于获得其氮杂环丁烷盐前体,定制的 NHC 很容易获得。许多手性 NHC 支架已被合成并在催化中进行了测试。在此,我们仅强调那些在手性过渡金属催化中实现高对映选择性的 NHC 结构。在手性 NHC 领域的简要介绍之后,本教程综述介绍了不同类别的手性 NHC,并提供了对配体要求和立体化学模型结构微调的指导。

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