JOURNAL ARTICLE

Advances in C−N Bond Formation via N‐Centered Radicals from N‐Aminopyridinium Reagents.

  • Published In: European Journal of Organic Chemistry, 2025, v. 28, n. 6. P. 1 1 of 3

  • Database: Academic Search Ultimate 2 of 3

  • Authored By: Sajjad, Farrukh; Lu, Cheng; Chen, Tie‐Gen 3 of 3

Abstract

Nitrogen‐centered radicals (NCRs) have gained significant attention due to their high reactivity, which facilitates many useful and challenging transformations, particularly in the formation of C−N bonds. In this regard, N‐aminopridinium reagents are easily accessible substrates that readily generate N‐centered radicals, which can be trapped by arenes, olefins, alkynes and even alkanes under visible light irradiation. In recent years, amination strategies involving N‐aminopyridinium salts have grown remarkably and attracted considerable interest within the synthetic community. This review comprehensively includes all the significant advances in C−N bond construction via N‐centered radicals derived from N‐aminopyridinium substrates. [ABSTRACT FROM AUTHOR]

Additional Information

  • Source:European Journal of Organic Chemistry. 2025/02, Vol. 28, Issue 6, p1
  • Document Type:Literature Review
  • Subject Area:Chemistry
  • Publication Date:2025
  • ISSN:1434-193X
  • DOI:10.1002/ejoc.202401220
  • Accession Number:183898697
  • Copyright Statement:Copyright of European Journal of Organic Chemistry is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

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