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Synthesis of Imidazopyridines via Copper-Catalyzed, Formal Aza-[3 + 2] Cycloaddition Reaction of Pyridine Derivatives with α-Diazo Oxime Ethers.

Sangjune ParkHyunseok KimJeong-Yu SonKyusik UmSooho LeeYonghyeon BaekBoram SeoPhil Ho Lee
Published in: The Journal of organic chemistry (2017)
The Cu-catalyzed, formal aza-[3 + 2] cycloaddition reaction of pyridine derivatives with α-diazo oxime ethers in trifluoroethanol was used to synthesize imidazopyridines via the release of molecular nitrogen and elimination of alcohol. These methods enabled modular synthesis of a wide range of N-heterobicyclic compounds such as imidazopyridazines, imidazopyrimidines, and imidazopyrazines with an α-imino Cu-carbenoid generated from the α-diazo oxime ethers and copper.
Keyphrases
  • structure activity relationship
  • aqueous solution
  • metal organic framework
  • oxide nanoparticles