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Cu-Catalyzed C(sp 3 ) Amination of Unactivated Secondary Alkyl Iodides Promoted by Diaryliodonium Salts.

Xin-Yang LvRúben Martín
Published in: Organic letters (2023)
Herein, we describe the development of a copper-catalyzed C(sp 3 ) amination of unactivated secondary alkyl iodides mediated by diaryliodonium salts. Our protocol is enabled by the intermediacy of aryl radical species that undergo halogen atom transfer prior to interfacing with copper catalysts, thus setting the basis for a C-N bond formation at sp 3 -hybridized carbons. The method is characterized by its mild reaction conditions, excellent regioselectivity, and wide substrate scope.
Keyphrases
  • ionic liquid
  • room temperature
  • randomized controlled trial
  • electron transfer
  • highly efficient
  • metal organic framework
  • molecular dynamics
  • transition metal
  • aqueous solution