化学
胺化
组合化学
芳基
亲核细胞
催化作用
生化工程
范围(计算机科学)
胺气处理
电化学
有机化学
电极
工程类
物理化学
计算机科学
程序设计语言
烷基
作者
Yu Kawamata,Julien C. Vantourout,David P. Hickey,Peng Bai,Longrui Chen,Qinglong Hou,Wenhua Qiao,Koushik Barman,Martin A. Edwards,Alberto F. Garrido‐Castro,Justine N. deGruyter,Hugh Nakamura,Kyle W. Knouse,Chuanguang Qin,Khalyd J. Clay,Deng‐Hui Bao,Chao Li,Jeremy T. Starr,Carmen N. García-Irizarry,Neal W. Sach
摘要
C-N cross-coupling is one of the most valuable and widespread transformations in organic synthesis. Largely dominated by Pd- and Cu-based catalytic systems, it has proven to be a staple transformation for those in both academia and industry. The current study presents the development and mechanistic understanding of an electrochemically driven, Ni-catalyzed method for achieving this reaction of high strategic importance. Through a series of electrochemical, computational, kinetic, and empirical experiments, the key mechanistic features of this reaction have been unraveled, leading to a second generation set of conditions that is applicable to a broad range of aryl halides and amine nucleophiles including complex examples on oligopeptides, medicinally relevant heterocycles, natural products, and sugars. Full disclosure of the current limitations and procedures for both batch and flow scale-ups (100 g) are also described.
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