Heterocyclic amines for the construction of peptoid oligomers bearing multi-dentate ligands

Galia Maayan, Barney Yoo, Kent Kirshenbaum

Research output: Contribution to journalArticle

Abstract

Peptoids are oligomers of N-substituted glycine that can be readily assembled using haloacetic acids and primary amines as synthons. Here, we report the synthesis and characterization of three new heterocyclic amines, 2-(2,2′:6′,2″-terpyridine-4′-yloxy)ethylamine, 2-(1,10-phenanthroline-5-yloxy)ethylamine and 8-hydroxy-2-quinolinemethylamine, and their incorporation into a series of different peptoid oligomer sequences. Since the heterocycles are all known to coordinate metal ions, the peptidomimetic products are designed to bind metal species with the potential for applications in catalysis and materials science.

Original languageEnglish (US)
Pages (from-to)335-338
Number of pages4
JournalTetrahedron Letters
Volume49
Issue number2
DOIs
StatePublished - Jan 7 2008

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Peptoids
Bearings (structural)
Oligomers
N-substituted Glycines
Amines
Metals
Ligands
Peptidomimetics
Materials science
Catalysis
Metal ions
Ions
Acids
ethylamine

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Heterocyclic amines for the construction of peptoid oligomers bearing multi-dentate ligands. / Maayan, Galia; Yoo, Barney; Kirshenbaum, Kent.

In: Tetrahedron Letters, Vol. 49, No. 2, 07.01.2008, p. 335-338.

Research output: Contribution to journalArticle

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