Direct coupling of inert C–H bonds in NHC organocatalysis

IF 4.6 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Chemistry Frontiers Pub Date : 2023-09-12 DOI:10.1039/D3QO01129A
Hongling Wang, Fen Su, Yanyan Wang, Xingxing Wu and Yonggui Robin Chi
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Abstract

Direct coupling of inert C–H bonds by N-heterocyclic carbenes (NHCs) represents a fascinating area of research in organocatalysis. Recently, several notable studies have disclosed the potential of NHCs to directly functionalize latent C–H bonds of diverse simple molecules (e.g., ethers, amines, and arenes). These methodologies offer straightforward and efficient routes for C–C bond-forming transformations by diminishing the need for prefunctionalization manipulations of inert C–H bonds, allowing for the synthesis of a broad range of high value-added functional ketone molecules. Consequently, this highlight aims to present the latest advancements in NHC organocatalysis, specifically focusing on direct coupling functionalization of inert C–H bonds involving the electron or proton transfer process (ET/PT pathways) and hydrogen atom transfer pathway (HAT pathway).

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NHC有机催化中惰性C–H键的直接偶联
N-杂环卡宾(NHCs)直接偶联惰性C–H键是有机催化研究的一个有趣领域。最近,几项著名的研究揭示了NHCs直接功能化各种简单分子(如醚、胺和芳烃)的潜在C–H键的潜力。这些方法通过减少对惰性C–H键的预官能化操作的需要,为C–C键的形成转化提供了直接有效的途径,从而可以合成广泛的高附加值功能酮分子。因此,本亮点旨在介绍NHC有机催化的最新进展,特别是涉及电子或质子转移过程(ET/PT途径)和氢原子转移途径(HAT途径)的惰性C–H键的直接偶联功能化。
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来源期刊
Organic Chemistry Frontiers
Organic Chemistry Frontiers CHEMISTRY, ORGANIC-
CiteScore
7.90
自引率
11.10%
发文量
686
审稿时长
1 months
期刊介绍: Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.
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