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Visible‐Light‐Mediated Functionalization of Aryl Diazonium Salts
Author(s) -
Zhang Xin,
Mei Yaoyao,
Li Yangyang,
Hu Jingang,
Huang Dayun,
Bi Yicheng
Publication year - 2021
Publication title -
asian journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.846
H-Index - 44
eISSN - 2193-5815
pISSN - 2193-5807
DOI - 10.1002/ajoc.202000636
Subject(s) - chemistry , aryl , reagent , isocyanide , surface modification , catalysis , combinatorial chemistry , coupling reaction , molecule , organic chemistry , metal , photochemistry , alkyl
Abstract Aryl diazonium salts are important molecules in organic chemistry. This review discusses advances of their application in light‐mediated reactions summarized in five categories according to the bond formations: (1) C−C formation from alkenes, alkynes, arenes, isocyanide, CO, arylboronic acid, or Grignard reagent. (2–5) C−B, C−N, C−S, and C−P formations. Reactions such as radical addition, elimination, metal‐catalyzed coupling, C−H activation, cyclizations, and rearrangements will be discussed herein.

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