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Accessing Medium-Sized Rings via Vinyl Carbocation Intermediates.

Authors :
Zhao Z
Popov S
Lee W
Burch JE
Delgadillo DA
Kim LJ
Shahgholi M
Lebrón-Acosta N
Houk KN
Nelson HM
Source :
Organic letters [Org Lett] 2024 Feb 09; Vol. 26 (5), pp. 1000-1005. Date of Electronic Publication: 2024 Jan 31.
Publication Year :
2024

Abstract

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.

Details

Language :
English
ISSN :
1523-7052
Volume :
26
Issue :
5
Database :
MEDLINE
Journal :
Organic letters
Publication Type :
Academic Journal
Accession number :
38295154
Full Text :
https://doi.org/10.1021/acs.orglett.3c04014