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Mechanism of Cu-Catalyzed Aryl Boronic Acid Halodeboronation Using Electrophilic Halogen: Development of a Base-Catalyzed Iododeboronation for Radiolabeling Applications.

John J MolloyKerry M O'RourkeCarolina P FriasNikki L SloanMatthew J WestSally L PimlottAndrew SutherlandAllan J B Watson
Published in: Organic letters (2019)
An investigation into the mechanism of Cu-catalyzed aryl boronic acid halodeboronation using electrophilic halogen reagents is reported. Evidence is provided to show that this takes place via a boronate-driven ipso-substitution pathway and that Cu is not required for these processes to operate: general Lewis base catalysis is operational. This in turn allows the rational development of a general, simple, and effective base-catalyzed halodeboronation that is amenable to the preparation of 125I-labeled products for SPECT applications.
Keyphrases
  • room temperature
  • aqueous solution
  • metal organic framework
  • sensitive detection
  • pet ct
  • high resolution
  • quantum dots
  • liquid chromatography