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Functionalization of C-H Bonds by Photoredox Catalysis.
Qin, Qixue; Jiang, Heng; Hu, Zhentao; Ren, Daan; Yu, Shouyun.
Afiliação
  • Qin Q; State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
  • Jiang H; State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
  • Hu Z; State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
  • Ren D; State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
  • Yu S; State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
Chem Rec ; 17(8): 754-774, 2017 08.
Article em En | MEDLINE | ID: mdl-28074599
ABSTRACT
Visible-light photoredox catalysis has been successfully used in the functionalization of inert C-H bonds including C(sp2 )-H bonds of arenes and C(sp3 )-H bonds of aliphatic compounds over the past decade. These transformations are typically promoted by the process of single-electron-transfer (SET) between substrates and photo-excited photocatalyst upon visible light irradiation (household bulbs or LEDs). Compared with other synthetic strategies, such as the transition-metal catalysis and traditional radical reactions, visible-light photoredox approach has distinct advantages in terms of operational simplicity and practicability. Versatile direct functionalization of inert C(sp2 )-H and C(sp3 )-H bonds including alkylation, trifluoromethylation, arylation and amidation, has been achieved using this practical strategy.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Chem Rec Assunto da revista: QUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Chem Rec Assunto da revista: QUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China