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Aryldiazonium Salt-Triggered [2 + 2 + 1] Heteroannulation of Indoles by an Arylhydrazone Radical-Relayed 1,5-Hydrogen Atom Transfer.

Jun-Yao OuyangFang-Fang ShenHan-Qing ZhaoJia-Jie ChenZhu-Dong WenHui-Min JiangJing-Hao QinQing SunJin-Heng LiXuan-Hui Ouyang
Published in: Organic letters (2023)
An unprecedented three-component [2 + 2 + 1] annulation cascade of indoles with aryldiazonium salts and polyhalomethanes or acetone is presented by dual hydrogen atom transfer (HAT) and C-H functionalization. By employing readily accessible aryldiazonium salts as the radical initiators and electrophiles and polyhalomethanes and acetone as the C1 units, this method unprecedentedly constructs a pyrazole ring on an indole ring skeleton through the formation of two C-N bonds and a C-C bond in a single reaction.
Keyphrases
  • electron transfer
  • ionic liquid
  • molecular dynamics
  • molecular docking
  • visible light