The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes

Org Biomol Chem. 2004 Sep 21;2(18):2664-70. doi: 10.1039/B409259G. Epub 2004 Aug 24.

Abstract

A number of chiral unsymmetrically N-substituted 1,4,7-triazacyclononane ligands have been prepared by modular methods. The key step in the synthesis centres on the macrocyclisation of three tertiary amide precursors under standard Richman-Atkins conditions which allows for subsequent N-functionalisation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Crystallography, X-Ray
  • Heterocyclic Compounds / chemical synthesis*
  • Heterocyclic Compounds / chemistry
  • Ligands
  • Molecular Structure
  • Oxidation-Reduction

Substances

  • Heterocyclic Compounds
  • Ligands
  • 1,4,7-triazacyclononane