Visible‐Light‐Mediated Functionalization of Aryl Diazonium Salts | Zendy

Zhang Xin | Zendy; Mei Yaoyao | Zendy; Li Yangyang | Zendy; Hu Jingang | Zendy; Huang Dayun | Zendy; Bi Yicheng | Zendy

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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

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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