Login / Signup

Near-Infrared-Light-Induced Iron(I) Dimer-Enabled Radical Cascade Reactions of Fluoroalkyl Bromides for the Synthesis of Ring-Fused Quinazolinones.

Xiao-Di SuQiang LiuJin-Tang ChengZhi-Xiang WangXiang-Yu Chen
Published in: Organic letters (2024)
The use of an earth-abundant and inexpensive iron complex as a catalyst, coupled with near-infrared (NIR) light as the energy source, for radical reactions with alkyl halides has been far less developed. In this study, we report NIR light-mediated iron(I) dimer-catalyzed radical cascade reactions of fluoroalkyl bromides for the synthesis of ring-fused quinazolinones bearing a difluoromethyl group. In this process, the 3-bromo-1,10-phenanthroline ligand facilitates the reactivity of [CpFe(CO) 2 ] 2 , thereby improving the efficiency of the reaction.
Keyphrases
  • iron deficiency
  • room temperature
  • photodynamic therapy
  • ionic liquid
  • drug release
  • fluorescence imaging
  • fluorescent probe
  • visible light
  • reduced graphene oxide
  • electron transfer