Volume 41, Issue 5 pp. 544-547
Emerging Topic

Nucleophilic Radicals as Hydrogen Atom Abstractors in C(sp3)-H Functionalization Reactions

Tao Li

Tao Li

State Key Laboratory of Physical Chemistry of Solid Surfaces, Key Laboratory of Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005 China

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Jian Li

Jian Li

State Key Laboratory of Physical Chemistry of Solid Surfaces, Key Laboratory of Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005 China

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Haohua Huo

Corresponding Author

Haohua Huo

State Key Laboratory of Physical Chemistry of Solid Surfaces, Key Laboratory of Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005 China

E-mail: [email protected]Search for more papers by this author
First published: 04 November 2022
Citations: 3

Comprehensive Summary

Hydrogen atom transfer (HAT) is an elementary mechanistic step in organic synthesis. The photoredox-catalyzed HAT has transformed organic synthesis by enabling the activation and subsequent cross-coupling of traditionally inert yet ubiquitous C(sp3)-H bonds. While diverse electrophilic radical species have proven to be exceptionally effective HAT catalysts for selective functionalization of hydridic and electron-neutral C(sp3)-H, general methods using nucleophilic radicals as hydrogen atom abstractors in C(sp3)-H functionalization remain relatively underdeveloped. Herein, we highlight two creative and strategic advances in addressing this long-standing challenge, and emphasize reaction achievements, mechanistic insights, potential, and future challenges. image

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