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Iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light.

Arona FallMihaela MagdeiMariia SavchukSylvain OudeyerHélène BeucherJean-François Brière
Published in: Chemical communications (Cambridge, England) (2024)
Herein, we disclose an eco-efficient redox-neutral iron-catalyzed decarboxylative radical addition to chiral azomethine imines upon visible light (427 nm) giving cyclic hydrazine derivatives with dr ranging from 82 : 18 to >96 : 4. This earth-abundant metal promoted sequence proceeds efficiently under ligand-free conditions based on a LMCT process and opens a route to new chiral heterocycles.
Keyphrases
  • visible light
  • capillary electrophoresis
  • ionic liquid
  • room temperature
  • mass spectrometry
  • photodynamic therapy
  • structure activity relationship
  • electron transfer