Mini-Reviews in Medicinal Chemistry

Author(s): Neelottama Kushwaha* and C.S. Sharma

DOI: 10.2174/1389557520666200729160720

DownloadDownload PDF Flyer Cite As
The Chemistry of Triazine Isomers: Structures, Reactions, Synthesis and Applications

Page: [2104 - 2122] Pages: 19

  • * (Excluding Mailing and Handling)

Abstract

Triazine is the six-membered heterocyclic ring containing three nitrogens, which replace the carbon-hydrogen unit in the benzene ring. Based on nitrogen position present in the ring system, it is categorized in three isomeric forms, i.e., 1, 2, 3-triazine (vicinal triazine), 1, 2, 4-triazine (asymmetrical triazine or isotriazine) and 1, 3, 5-triazine (symmetrical or s-triazine or cyanidine). Triazines have a weakly basic property. Their isomers have much weaker resonance energy than benzene structure, so nucleophilic substitution reactions are more preferred than electrophilic substitution reactions. Triazine isomers and their derivatives are known to play important roles possessing various activities in medicinal and agricultural fields such as anti-cancer, antiviral, fungicidal, insecticidal, bactericidal, herbicidal, antimalarial and antimicrobial agents.

Keywords: Heterocyclic, triazines, chemical reactivity, triazine synthesis, potent, biological activity.