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Copper-Catalyzed Chemoselective Silylative Cyclization of 2,2'-Diethynylbiaryl Derivatives.

Meng ZhaoYing WangZi-Lu WangJian-Lin XuKai-Yang DaiYun-He Xu
Published in: Organic letters (2021)
In this protocol, copper-catalyzed diverse silylative carbocyclization reactions of 2,2'-diethynylbiaryl derivatives with silaboronate were reported. Three new and novel types of domino reactions for the copper-catalyzed transformation of silaboronate were discovered. The corresponding cyclobuta[l]phenanthrene, bis((silyl)methyl)phenanthrene, and silyl-substituted exocyclic diene products were chemoselectively formed with high efficiency.
Keyphrases
  • high efficiency
  • structure activity relationship
  • randomized controlled trial
  • molecular docking
  • ionic liquid