Transition Metal-Catalyzed Remote C–H Bond Functionalization of Cyclic Amines

IF 2 Q2 CHEMISTRY, ORGANIC
SynOpen Pub Date : 2022-08-24 DOI:10.1055/a-1929-9789
Weijie Chen, Xiaoyu Yang, Xiaobei Cao
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引用次数: 1

Abstract

C–H bond functionalization is one of the most effective strategies for the rapid synthesis of cyclic amines containing substituents in the ring, which are core structures of many bioactive molecules. It is, however, much more challenging to perform this strategy on remote C–H bonds compared to α-C–H bonds of cyclic amines. This graphical review aims to provide a concise overview on transition metal-catalyzed methods for the remote C–H bond functionalization of cyclic amines. Examples are categorized and demonstrated according to mechanistic pathways that initiate the reaction of cyclic amine substrates. Selected substrate scope and detailed reaction mechanisms are given when necessary.
过渡金属催化环胺的远端C-H键功能化
碳-氢键功能化是快速合成含取代基环胺的最有效方法之一,而环胺是许多生物活性分子的核心结构。然而,与环胺的α-C-H键相比,在远端C-H键上执行该策略更具挑战性。本文简要介绍了过渡金属催化环胺远端C-H键功能化的方法。根据启动环胺底物反应的机制途径对实例进行分类和论证。必要时给出了选定的底物范围和详细的反应机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
SynOpen
SynOpen CHEMISTRY, ORGANIC-
CiteScore
2.30
自引率
4.00%
发文量
35
审稿时长
6 weeks
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