Login / Signup

Copper-catalyzed multiple oxidation and cycloaddition of aryl-alkyl ketones (alcohols) for the synthesis of 4-acyl- and 4-diketo-1,2,3-triazoles.

Liangfeng HuangLei ZhengZhong-Zhen ZhouYunfeng Chen
Published in: Chemical communications (Cambridge, England) (2022)
A Cu/TEMPO-catalyzed tandem multiple oxidative dehydrogenation and cycloaddition has been developed, which affords 4-acyl-1,2,3-triazoles and 4-diketo-1,2,3-triazoles from readily-available aryl-alkyl ketones (or alcohols) and different organic azides. Moreover, the reaction used environmentally friendly dimethyl carbonate (DMC) as the solvent and air as the oxidant, and H 2 O was the only by-product, so it provides a green and practical synthetic method for 1,2,3-triazoles.
Keyphrases
  • ionic liquid
  • room temperature
  • fatty acid
  • hydrogen peroxide
  • nitric oxide
  • electron transfer
  • aqueous solution