Deproto-metallation and computed CH acidity of 2-aryl-1,2,3-triazoles

Org Biomol Chem. 2012 Jul 7;10(25):4878-85. doi: 10.1039/c2ob25554e. Epub 2012 May 21.

Abstract

2-Aryl-1,2,3-triazoles were synthesized by cyclization of the corresponding glyoxal arylosazones, generated from commercial arylhydrazines. The deproto-metallation of 2-phenyl-1,2,3-triazole was attempted using different 2,2,6,6-tetramethylpiperidino-based mixed lithium-metal (Zn, Cd, Cu, Co, Fe) combinations, giving results in the case of Zn, Cd, and Cu. The lithium-zinc combination was next selected to apply the deprotonation-iodination sequence to all the 2-aryl-1,2,3-triazoles synthesized. The results were analyzed with the help of the CH acidities of the substrates, determined in THF solution using the DFT B3LYP method.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acids / chemistry
  • Metals / chemistry*
  • Models, Molecular
  • Molecular Structure
  • Triazoles / chemical synthesis*

Substances

  • Acids
  • Metals
  • Triazoles