Aryl radical-mediated N-heterocyclic carbene catalysis

• Published in: Nature communications Vol. 12; no. 1; p. 3848
• Main Authors: Matsuki, Yuki, Ohnishi, Nagisa, Kakeno, Yuki, Takemoto, Shunsuke, Ishii, Takuya, Nagao, Kazunori, Ohmiya, Hirohisa
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 22.06.2021; Nature Publishing Group; Nature Portfolio
• Subjects: 140/131; 140/58; 639/638/403/933; 639/638/77/885; 639/638/77/889; Acylation; Aldehydes; Amides; Aromatic compounds; Catalysis; Chemical reactions; Chemical synthesis; Electron transfer; Halides; Humanities and Social Sciences; Iodides; Metals; multidisciplinary; Oxidants; Oxidizing agents; Radicals; Reagents; Reducing agents; Science; Science (multidisciplinary); Single electrons; Styrenes; Transition metals
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-021-24144-2

There have been significant advancements in radical reactions using organocatalysts in modern organic synthesis. Recently, NHC-catalyzed radical reactions initiated by single electron transfer processes have been actively studied. However, the reported examples have been limited to catalysis mediated by alkyl radicals. In this article, the NHC organocatalysis mediated by aryl radicals has been achieved. The enolate form of the Breslow intermediate derived from an aldehyde and thiazolium-type NHC in the presence of a base undergoes single electron transfer to an aryl iodide, providing an aryl radical. The catalytically generated aryl radical could be exploited as an arylating reagent for radical relay-type arylacylation of styrenes and as a hydrogen atom abstraction reagent for α-amino C(sp 3 )–H acylation of secondary amides. Use of aryl halides as coupling precursors typically occurs through transition metal catalysis and/or photoredox chemistry, which requires some combination of light, metals, and oxidants or reductants. Here, the authors show a method to generate aryl radicals from halides using only an NHC organocatalyst.