烷基化
催化作用
镍
小学(天文学)
化学
基质(水族馆)
范围(计算机科学)
组合化学
功能群
布朗斯特德-洛瑞酸碱理论
基础(拓扑)
歧管(流体力学)
电化学
有机化学
计算机科学
物理化学
物理
机械工程
数学分析
海洋学
聚合物
数学
电极
天文
工程类
程序设计语言
地质学
作者
Ramesh C. Samanta,Julia Struwe,Lutz Ackermann
标识
DOI:10.1002/anie.202004958
摘要
Abstract Direct alkylations of carboxylic acid derivatives are challenging and particularly nickel catalysis commonly requires high reaction temperatures and strong bases, translating into limited substrate scope. Herein, nickel‐catalyzed C−H alkylations of unactivated 8‐aminoquinoline amides have been realized under exceedingly mild conditions, namely at room temperature, with a mild base and a user‐friendly electrochemical setup. This electrocatalyzed C−H alkylation displays high functional group tolerance and is applicable to both the primary and secondary alkylation. Based on detailed mechanistic studies, a nickel(II/III/I) catalytic manifold has been proposed.
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