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Photocatalytic synthesis of azaheterocycle-fused piperidines and pyrrolidines via tandem difunctionalization of unactivated alkenes.

Qun-Huai ZhouJia-Ying DaiWen-Jing ZhaoXi-Ya ZhongChun-Yang LiuWei-Wei LuoZhi-Wei LiJiang-Sheng LiWei-Dong Liu
Published in: Organic & biomolecular chemistry (2023)
A variety of azaheterocycle-fused piperidines and pyrrolidines bearing CF 3 and CHF 2 functionalities were obtained using CF 3 SO 2 Na and CHF 2 SO 2 Na by visible light photocatalysis. This protocol involves a radical cascade cyclization via tandem tri- and difluoromethylation-arylation of pendent unactivated alkenes. Benzimidazole, imidazole, theophylline, purine, and indole serve as applicable anchors, thereby enriching the structural diversity of piperidine and pyrrolidine derivatives. This method features mild, additive-free and transition metal-free conditions.
Keyphrases
  • visible light
  • cystic fibrosis
  • randomized controlled trial
  • molecular docking