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Synthesis of imidazo[1,2- a ]benzoazepines by alkyne-carbonyl-metathesis.

Maryam SobhaniRúben Manuel Figueira de AbreuAlexander VillingerPeter EhlersPeter Langer
Published in: Organic & biomolecular chemistry (2022)
Imidazo[1,2- a ]benzoazepines were prepared by Brønsted acid-mediated intramolecular alkyne-carbonyl metathesis (ACM). The starting materials, imidazole and benzimidazole derivatives, were prepared by N -alkylation, formylation and Sonogashira cross-coupling reaction. The final intramolecular ACM delivered the final products in good to excellent yields and with a wide tolerance towards functional groups.
Keyphrases
  • energy transfer
  • molecular docking
  • structure activity relationship
  • quantum dots