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Phosphine-Catalyzed (4 + 2) Annulation of δ-Sulfonamido-Substituted Enones with 1,1-Dicyanoalkenes: Synthesis of Piperidine Derivatives.

Min LiuLeijie ZhouWangyu ShiYimin HuJianning LiaoZeqing DuanWei WangYongjun WuBing ZhengHongchao Guo
Published in: Organic letters (2021)
The δ-sulfonamido-substituted enones were employed as phosphine acceptor in phosphine-catalyzed (4 + 2) annulation of 1,1-dicyanoalkenes. They served as a four-membered synthon to react with 1,1-dicyanoalkenes under mild reaction conditions, producing piperidine derivatives in moderate to excellent yields with good to excellent diastereoselectivities.
Keyphrases
  • molecular docking
  • room temperature
  • structure activity relationship
  • high intensity
  • energy transfer
  • ionic liquid
  • molecular dynamics simulations
  • electron transfer