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A General Approach for the Synthesis of Cyanoisopropyl Bicyclo[1.1.1]pentane (BCP) Motifs by Energy Transfer Process.

Lin LiQing PangBinbin ChenYumiao LiuYuxuan ZhaoJirong WuKai GeJiabin ShenPeng-Fei Zhang
Published in: Organic letters (2024)
Bicyclo[1.1.1]pentane (BCP) heteroaryls make up an important class of BCP derivatives in drug discovery. Herein, we report the visible-light-mediated synthesis of cyanoisopropyl BCP-heteroaryls motifs from N -containing heterocycles, [1.1.1]propellane, and AIBN (2,2'-azobis(isobutyronitrile)) through three-component cascade reaction. Importantly, this protocol is compatible with pyrazinones, quinoxaline-2( 1H )-one, azauracils, quinoline derivatives, and imidazo[1,2- b ]pyridazine, as well as various phenyl disulfide derivatives; thus, this operationally simple and general methodology could enable rapid library generation of sought-after BCP derivatives for drug development.
Keyphrases
  • drug discovery
  • energy transfer
  • visible light
  • structure activity relationship
  • randomized controlled trial
  • quantum dots
  • molecular dynamics simulations