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Cu(I)-Catalyzed Coupling and Cycloisomerization of Diazo Compounds with Terminal Yne-Alkylidenecyclopropanes: Synthesis of Functionalized Cyclopenta[ b]naphthalene Derivatives.

Peng-Hua LiLiu-Zhu YuXiao-Yu ZhangMin Shi
Published in: Organic letters (2018)
A Cu(I)-catalyzed coupling and cycloisomerization of diazo compounds with terminal yne-alkylidenecyclopropanes (ACPs) has been presented. This reaction starts from the formation of an allenic intermediate in the Cu(I)-catalyzed cross-coupling reaction of a diazo compound with terminal alkyne in yne-tethered ACP and then undergoes a domino cycloisomerization of a 6π-electrocyclization and cyclopropane ring-opening rearrangement to give functionalized cyclopenta[ b]naphthalene derivatives in moderate to excellent yields under mild conditions.
Keyphrases
  • room temperature
  • aqueous solution
  • ionic liquid
  • quantum dots
  • metal organic framework
  • electron transfer
  • molecularly imprinted
  • structure activity relationship
  • mass spectrometry
  • liquid chromatography