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C(sp3)–H Bond Acylation with N-Acyl Imides under Photoredox/ Nickel Dual Catalysis
Synlett ( IF 2 ) Pub Date : 2020-10-08 , DOI: 10.1055/s-0040-1707301
Abderrahmane Amgoune 1, 2 , Taline Kerackian 1 , Antonio Reina 1 , Tetiana Krachko 1 , Hugo Boddaert 1 , Didier Bouyssi 1 , Nuno Monteiro 1
Affiliation  

A novel Ni/photoredox-catalyzed acylation of aliphatic substrates, including simple alkanes and dialkyl ethers, has been developed. The method combines C–N bond activation of amides with a radical relay mechanism involving hydrogen-atom transfer. The protocol is operationally simple, employs bench-stable N-acyl imides as acyl-transfer reagents, and permits facile access to alkyl ketones under very mild conditions.

中文翻译:

在光氧化还原/镍双催化下与 N-酰基酰亚胺的 C(sp3)-H 键酰化

已经开发了一种新型的 Ni/光氧化还原催化的脂肪族底物酰化,包括简单的烷烃和二烷基醚。该方法将酰胺的 C-N 键活化与涉及氢原子转移的自由基中继机制相结合。该协议操作简单,采用长期稳定的 N-酰基酰亚胺作为酰基转移试剂,并允许在非常温和的条件下轻松获得烷基酮。
更新日期:2020-10-08
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