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Redox Reactions of Organic Molecules Using Rotating Magnetic Field and Metal Rods.
Liu, Haodong; Han, Xuliang; Feng, Xiaomei; Zhang, Lizhi; Sun, Fenggang; Jia, Fuchao; Zhao, Zengdian; Liu, Hui; Li, Xinjin.
Afiliación
  • Liu H; School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong 255000, China.
  • Han X; School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong 255000, China.
  • Feng X; School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong 255000, China.
  • Zhang L; School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong 255000, China.
  • Sun F; School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong 255000, China.
  • Jia F; School of Physics and Optoelelctronic Engineering, Shandong University of Technology, Zibo, Shandong 255000, China.
  • Zhao Z; School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong 255000, China.
  • Liu H; School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong 255000, China.
  • Li X; School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong 255000, China.
J Am Chem Soc ; 146(26): 18143-18150, 2024 Jul 03.
Article en En | MEDLINE | ID: mdl-38916056
ABSTRACT
In recent years, redox reactions have harnessed light or mechanical energy to enable the formation of chemical bonds. We postulated a complementary approach that electromagnetic induction could promote the redox reaction of organic molecules using a rotating magnetic field and metal rods. Here, we report that electromotive force activates the redox-active trifluoromethylating reagents. This magnetoredox system can be applied to the trifluoromethylation of heteroarenes with high regioselectivity and hydrotrifluoromethylation of alkenes without the need for catalysts and organic additives.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2024 Tipo del documento: Article País de afiliación: China