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<i>N</i>,<i>N</i>,<i>N</i>’,<i>N</i>’-Tetramethylethylenediamine-Enabled Photoredox-Catalyzed C–H Methylation of <i>N</i>-Heteroarenes

Fang Liu, Zhipeng Ye, Yuan‐Zhuo Hu, Jie Gao, Lan Zheng, Kai Chen, Hao‐Yue Xiang, Xiaoqing Chen, Hua Yang

2021The Journal of Organic Chemistry29 citationsDOI

Abstract

Aiming at the valuable methylation process, readily available and inexpensive N,N,N′,N′-tetramethylethylenediamine (TMEDA) was first identified as a new methyl source in photoredox-catalyzed transformation in this work. By virtue of this simple methylating reagent, a facile and practical protocol for the direct C–H methylation of N-heteroarenes was developed, featuring mild reaction conditions, broad substrate scope, and scalability. Mechanistic studies disclosed that a sequential photoredox, base-assisted proton shift, fragmentation, and tautomerization process was essentially involved.

Topics & Concepts

TetramethylethylenediamineMethylationChemistryCatalysisMedicinal chemistryOrganic chemistryBiochemistryGeneCatalytic C–H Functionalization MethodsRadical Photochemical ReactionsSulfur-Based Synthesis Techniques
<i>N</i>,<i>N</i>,<i>N</i>’,<i>N</i>’-Tetramethylethylenediamine-Enabled Photoredox-Catalyzed C–H Methylation of <i>N</i>-Heteroarenes | Litcius