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Accessing Medium-Sized Rings via Vinyl Carbocation Intermediates.

Zhenqi ZhaoStasik PopovWoojin LeeJessica E BurchDavid A DelgadilloLee Joon KimMona ShahgholiNaiara Lebrón-AcostaKendall N HoukHosea M Nelson
Published in: Organic letters (2024)
Medium-sized rings (8-11-membered cycles) are often more challenging to synthesize than smaller rings (5-7-membered cycles) due to ring strain. Herein, we report a catalytic method for forming 8- and 9-membered rings that proceeds via the intramolecular Friedel-Crafts reactions of vinyl carbocation intermediates. These reactive species are generated catalytically through the ionization of vinyl toluenesulfonates by a Lewis acidic lithium cation-weakly coordinating anion salt.
Keyphrases
  • ionic liquid
  • mass spectrometry
  • solid state