Diazonium Salts as Nitrogen-Based Lewis Acids

Open Access
Authors
Publication date 05-2019
Journal Synlett
Volume | Issue number 30 | 8
Pages (from-to) 875-884
Number of pages 10
Organisations
  • Faculty of Science (FNWI) - Van 't Hoff Institute for Molecular Sciences (HIMS)
Abstract
Aryldiazonium salts are widely used in many organic transformations with displacement of N2 or through addition to the terminal nitrogen. Such aryldiazonium salts can be viewed as N-based Lewis acids that can react with Lewis bases to synthesize a wide variety of azo compounds. Additionally, diazonium salts are known to undergo single-electron transfer and release N2, forming an aryl radical, which results in different reactivity. Herein, we provide a concise overview of the reactivity of aryldiazonium salts undergoing classical donor-acceptor reactivity or single-electron transfer.
Document type Article
Language English
Published at https://doi.org/10.1055/s-0037-1612109
Downloads
Diazonium Salts (Final published version)
Permalink to this page
Back