Visible-Light-Induced Radical Cascade Cross-Coupling via C(sp3)-H Activation and C-N/N-O Cleavage: Feasible Access to Methylenebisamide Derivatives

被引:6
|
作者
Lei, Jinglan [1 ,2 ]
Li, Min [2 ]
Zhang, Qingqing [1 ]
Liu, Shuyang [1 ]
Li, Haifang [3 ]
Shi, Lei [1 ]
Jiang, Wen-Feng [2 ]
Duan, Chunying [1 ]
Jin, Yunhe [1 ]
机构
[1] Dalian Univ Technol, Zhang Dayu Sch Chem, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Dalian Univ Technol, Sch Chem Engn, Expt Ctr Chem, Dalian 116024, Peoples R China
[3] Tsinghua Univ, Dept Chem, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
ACID; BISAMIDES; BONDS;
D O I
10.1021/acs.orglett.3c00646
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Here we report facile and manipulable access to methylenebisamide derivatives via visible-light-driven radical cascade processes incorporating C(sp3)-H activation and C-N/ N-O cleavage. Mechanistic studies reveal that a traditional Ir-catalyzed photoredox pathway and a novel copper-induced complex-photolysis pathway are both involved, contributing to activating the inert N-methoxyamides and rendering the valuable bisamides. This approach exhibits many advantages, including mild reaction conditions, broad scope and functional group tolerance, and competitive step economy. Given the mechanistic plenitude and operational simplicity, we believe this package deal paves a promising way for the synthesis of valuable nitrogen-containing molecules.
引用
收藏
页码:2300 / 2305
页数:6
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