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N-Methylation of Amines with Methanol in the Presence of Carbonate Salt Catalyzed by a Metal-Ligand Bifunctional Ruthenium Catalyst [(p-cymene)Ru(2,2'-bpyO)(H2O)].
Liu, Peng; Tung, Nguyen Thanh; Xu, Xiangchao; Yang, Jiazhi; Li, Feng.
  • Liu P; School of Chemical Engineering, Nanjing University of Science & Technology, Nanjing 210094, People's Republic of China.
  • Tung NT; School of Chemical Engineering, Nanjing University of Science & Technology, Nanjing 210094, People's Republic of China.
  • Xu X; School of Chemical Engineering, Nanjing University of Science & Technology, Nanjing 210094, People's Republic of China.
  • Yang J; School of Chemical Engineering, Nanjing University of Science & Technology, Nanjing 210094, People's Republic of China.
  • Li F; School of Chemical Engineering, Nanjing University of Science & Technology, Nanjing 210094, People's Republic of China.
J Org Chem ; 86(3): 2621-2631, 2021 Feb 05.
Article en En | MEDLINE | ID: mdl-33502847
ABSTRACT
A ruthenium complex [(p-cymene)Ru(2,2'-bpyO)(H2O)] was found to be a general and efficient catalyst for the N-methylation of amines with methanol in the presence of carbonate salt. Moreover, a series of sensitive substituents, such as nitro, ester, cyano, and vinyl groups, were tolerated under present conditions. It was confirmed that OH units in the ligand are crucial for the catalytic activity. Notably, this research exhibited the potential of metal-ligand bifunctional ruthenium catalysts for the hydrogen autotransfer process.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2021 Tipo del documento: Article