4.2 Article

Azides - Diazonium Ions - Triazenes: Versatile Nitrogen-rich Functional Groups

Journal

AUSTRALIAN JOURNAL OF CHEMISTRY
Volume 67, Issue 3, Pages 328-336

Publisher

CSIRO PUBLISHING
DOI: 10.1071/CH13533

Keywords

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Funding

  1. German Science foundation [BR 1750, KSOP, CFN, TR88, SFB 380, SFB 624]
  2. Helmholtz Society
  3. Fonds der Chemischen Industrie

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For more than 100 years, nitrogen-rich compounds such as azides, diazonium ions, and triazenes have proved to be extremely valuable. Because these functional groups can be easily introduced into various substrates, they are frequently used nowadays. More importantly, they can be converted into a great number of other functional groups. The scope of this article is thus to summarize possible synthetic routes for the formation of these functional groups as well as to highlight some of the most prominent applications of these exciting moieties in chemical biology and combinatorial chemistry. Many of the most famous name reactions such as the Staudinger reduction, Staudinger ligation, Sandmeyer reaction, Wallach reaction, Mitsunobu reaction, Huisgen reaction, Balz-Schiemann reaction, Meerwein arylation, Pschorr reaction or Gomberg-Bachmann reaction are covered.

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