Accessing Medium-Sized Rings via Vinyl Carbocation Intermediates

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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Organic letters 2024-02, Vol.26 (5), p.1000-1005
Hauptverfasser: Zhao, Zhenqi, Popov, Stasik, Lee, Woojin, Burch, Jessica E., Delgadillo, David A., Kim, Lee Joon, Shahgholi, Mona, Lebrón-Acosta, Naiara, Houk, K. N., Nelson, Hosea M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung: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.
ISSN:1523-7060
1523-7052
1523-7052
DOI:10.1021/acs.orglett.3c04014