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N,N,N',N'-Tetramethylethylenediamine-Enabled Photoredox-Catalyzed C-H Methylation of N-Heteroarenes.
Liu, Fang; Ye, Zhi-Peng; Hu, Yuan-Zhuo; Gao, Jie; Zheng, Lan; Chen, Kai; Xiang, Hao-Yue; Chen, Xiao-Qing; Yang, Hua.
Afiliación
  • Liu F; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Ye ZP; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Hu YZ; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Gao J; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Zheng L; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Chen K; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Xiang HY; Key Laboratory of Chemical Oncogenomics, Peking University Shenzhen Graduate School, Shenzhen 518055, P. R. China.
  • Chen XQ; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
  • Yang H; College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, P. R. China.
J Org Chem ; 86(17): 11905-11914, 2021 09 03.
Article en En | MEDLINE | ID: mdl-34344150
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protones / Etilenodiaminas Tipo de estudio: Guideline Idioma: En Revista: J Org Chem Año: 2021 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protones / Etilenodiaminas Tipo de estudio: Guideline Idioma: En Revista: J Org Chem Año: 2021 Tipo del documento: Article Pais de publicación: Estados Unidos