化学
反应性(心理学)
路易斯酸
重氮化合物
芳基
电子转移
氮气
有机化学
接受者
高分子化学
组合化学
催化作用
烷基
病理
物理
医学
替代医学
凝聚态物理
作者
Evi R. M. Habraken,Andrew R. Jupp,J. Chris Slootweg
出处
期刊:Synlett
[Thieme Medical Publishers (Germany)]
日期:2019-02-08
卷期号:30 (08): 875-884
被引量:19
标识
DOI:10.1055/s-0037-1612109
摘要
Aryldiazonium salts are widely used in many organic transformations with displacement of N2 or through addition to the terminal nitrogen. Such aryldiazonium salts can be viewed as N-based Lewis acids that can react with Lewis bases to synthesize a wide variety of azo compounds. Additionally, diazonium salts are known to undergo single-electron transfer and release N2, forming an aryl radical, which results in different reactivity. Herein, we provide a concise overview of the reactivity of aryldiazonium salts undergoing classical donor-acceptor reactivity or single-electron transfer.
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