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Visible-Light-Induced Regioselective C(sp3)-H Acyloxylation of Aryl-2H-azirines with (Diacetoxy)iodobenzene.

Aramita DeSougata SantraAlakananda HajraGrigory V ZyryanovAdinath Majee
Published in: The Journal of organic chemistry (2019)
A visible-light-promoted regioselective coupling of C(sp3)-H of aryl-2H-azirine and (diacetoxy)iodobenzene has been reported. Rose Bengal as an organophotoredox catalyst has been used in this reaction. The reaction proceeds under aerobic condition at room temperature. A variety of aryl-2H-azirines gives the corresponding acyloxylated azirines under this reaction conditions. The reaction goes through a radical pathway. The protocol is also applicable on gram-scale synthesis.
Keyphrases
  • visible light
  • room temperature
  • ionic liquid
  • electron transfer
  • high glucose
  • gram negative
  • oxidative stress
  • reduced graphene oxide