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Chinese Journal of Organic Chemistry >

2022 , Vol. 42 >Issue 12: 4099 - 4110

DOI: https://doi.org/10.6023/cjoc202207019

REVIEWS

Progress of N-Amino Pyridinium Salts as Nitrogen Radical Precursors in Visible Light Induced C—N Bond Formation Reactions

  • Shaohui Yang ,
  • Jingcheng Song ,
  • Daoqing Dong ,
  • Hao Yang ,
  • Mengyu Zhou ,
  • Huishu Zhang ,
  • Zuli Wang
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  • College of Chemistry and Pharmaceutical Sciences, Qingdao Agricultural University, Qingdao, Shandong 266109
†These authors contributed equally to this work.
*E-mail:

Received date: 2022-07-08

  Revised date: 2022-08-26

  Online published: 2022-10-10

Supported by

National Natural Science Foundation of China(21772107)

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Abstract

Because of the redox properties of pyridine salt, it is found that N-amino pyridine salt plays an important role in free radical chemistry. N-Amino pyridinium salts easily undergo single electron reduction and N—N bond fragmentation to deliver N radicals. In this review, the advances of N-amino pyridinium salt serves as a powerful nitrogen radical precursor in visible light induced reactions for C—N bond formation are summarized in the last three years. According to the reaction substrates, the review is divided into three parts: react with arenes, react with olefins, and react with alkanes.

Key words： pyridinium salts; radical; visible light; green organic synthesis

Cite this article

Shaohui Yang , Jingcheng Song , Daoqing Dong , Hao Yang , Mengyu Zhou , Huishu Zhang , Zuli Wang . Progress of N-Amino Pyridinium Salts as Nitrogen Radical Precursors in Visible Light Induced C—N Bond Formation Reactions[J]. Chinese Journal of Organic Chemistry, 2022 , 42(12) : 4099 -4110 . DOI: 10.6023/cjoc202207019

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