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Lewis Acid-Catalyzed Diastereoselective Synthesis of Multisubstituted N-Acylaziridine-2-carboxamides from 2 H-Azirines via Joullié-Ugi Three-Component Reaction.

Anikó AngyalAndrás DemjénEdit WéberAnita K KovácsJános WölflingLászló G PuskásIván Kanizsai
Published in: The Journal of organic chemistry (2018)
A ZnCl2-catalyzed diastereoselective Joullié-Ugi three-component reaction from 2 H-azirines, isocyanides, and carboxylic acids was established. The protocol allows the preparation of highly and diversely functionalized N-acylaziridine-2-carboxamide derivatives in up to 82% isolated yields. Moreover, the applicability of N-acylaziridines is demonstrated through a variety of transformations.
Keyphrases
  • room temperature
  • molecularly imprinted
  • randomized controlled trial
  • electron transfer
  • ionic liquid
  • high resolution
  • mass spectrometry
  • structure activity relationship