Stable organogels derived from triazines functionalized with chiral alpha-amino acid derivatives

Raffella Maffezzoni, Matteo Zanda

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Triazines functionalized with three stereogenic alpha-amino-acidic appendages having at least one amide or hydroxamate function give highly stable organogels in haloalkanes and aromatic solvents, and their gelating ability depends on both structural and stereochemical properties. (C) 2008 Elsevier Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)5129-5132
Number of pages4
JournalTetrahedron Letters
Volume49
Issue number35
Early online date27 Jun 2008
DOIs
Publication statusPublished - 25 Aug 2008

Keywords

  • organogel
  • triazine
  • melamine
  • alpha-amino acids
  • hydroxamic acids
  • molecular-mass gelators
  • organic liquids
  • gelation
  • gels
  • template
  • length
  • water

Cite this

Stable organogels derived from triazines functionalized with chiral alpha-amino acid derivatives. / Maffezzoni, Raffella; Zanda, Matteo.

In: Tetrahedron Letters, Vol. 49, No. 35, 25.08.2008, p. 5129-5132.

Research output: Contribution to journalArticle

Maffezzoni, Raffella ; Zanda, Matteo. / Stable organogels derived from triazines functionalized with chiral alpha-amino acid derivatives. In: Tetrahedron Letters. 2008 ; Vol. 49, No. 35. pp. 5129-5132.
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