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...
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Veröffentlicht in: | Organic letters 2024-02, Vol.26 (5), p.1000-1005 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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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. |
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ISSN: | 1523-7060 1523-7052 1523-7052 |
DOI: | 10.1021/acs.orglett.3c04014 |