Next Article in Journal
Screening Analyses of Pinosylvin Stilbenes, Resin Acids and Lignans in Norwegian Conifers
Previous Article in Journal
Reactions of 9-Alkyl-3-aminocarbazoles with Ethyl-3-oxo-butanoate and Identification of the Products Obtained
Article Menu

Export Article

Open AccessArticle
Molecules 2006, 11(1), 81-102; doi:10.3390/11010081

Synthesis of 2,4,6-Tri-substituted-1,3,5-Triazines

CQFM, Departamento de Engenharia Química, Instituto Superior Técnico, 1049-001 Lisboa, Portugal
REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica, Portugal
Author to whom correspondence should be addressed.
Received: 21 June 2005 / Revised: 8 September 2005 / Accepted: 8 September 2005 / Published: 31 January 2006
View Full-Text   |   Download PDF [158 KB, uploaded 18 June 2014]   |  


Several specific synthetic protocols were developed for the preparation from cyanuric chloride of a range of symmetric and non-symmetric di- and tri-substituted 1,3,5-triazines containing alkyl, aromatic, hindered, chiral and achiral hydroxyalkyl, ester and imidazole groups via sequential nucleophilic substitution of the C-Cl bond by C-O, C-N and C-S bonds.
Keywords: Cyanuric chloride; s-triazine; 1; 3; 5-triazine; melamine derivatives. Cyanuric chloride; s-triazine; 1; 3; 5-triazine; melamine derivatives.
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

Scifeed alert for new publications

Never miss any articles matching your research from any publisher
  • Get alerts for new papers matching your research
  • Find out the new papers from selected authors
  • Updated daily for 49'000+ journals and 6000+ publishers
  • Define your Scifeed now

SciFeed Share & Cite This Article

MDPI and ACS Style

Afonso, C.A.M.; Lourenco, N.M.T.; Rosatella, A.A. Synthesis of 2,4,6-Tri-substituted-1,3,5-Triazines. Molecules 2006, 11, 81-102.

Show more citation formats Show less citations formats

Related Articles

Article Metrics

Article Access Statistics



[Return to top]

Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert
Back to Top