4.6 Review

Functionalization of C-H Bonds by Photoredox Catalysis

Journal

CHEMICAL RECORD
Volume 17, Issue 8, Pages 754-774

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/tcr.201600125

Keywords

visible light; photoredox; C-H functionalization; radical; photochemistry

Funding

  1. National Natural Science Foundation of China [21472084, 21672098]

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Visible-light photoredox catalysis has been successfully used in the functionalization of inert C-H bonds including C(sp(2))-H bonds of arenes and C(sp(3))-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(sp(2))-H and C(sp(3))-H bonds including alkylation, trifluoromethylation, arylation and amidation, has been achieved using this practical strategy.

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