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Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation.

Bojan VulovicMilena TrmcicRadomir MatovicRadomir N Saicic
Published in: Organic letters (2019)
Unsaturated oxyallyl cations with a suitably positioned alkene bond undergo 5-exo-cyclization with the formation of vinylcyclopentane derivatives. Alkyne analogues provide allenes. The reaction proceeds with a moderate to excellent level of stereoselectivity and allows for asymmetric induction in the reaction with chiral substrate.
Keyphrases
  • ionic liquid
  • structure activity relationship
  • electron transfer
  • high intensity
  • molecular docking
  • amino acid