Meta ‐Dimethylation of Arenes via Catellani Reaction from Aryl Thianthrenium Salts
Abstract: Here we report the reaction of aryl thianthrenium salts that allows selective functionalization of the meta position of arenes. The combination of a site‐selective thianthrenation with a Catellani reaction provides access to 3,5‐dimethylated arenes. The developed reaction is complementary to the previously discovered reductive ipso‐alkylation of aryl thianthrenium salts and extends the possibilities for late‐stage methylation of arenes with a single aryl thianthrenium salt.
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Meta ‐Dimethylation of Arenes via Catellani Reaction from Aryl Thianthrenium Salts ; day:25 ; month:11 ; year:2024 ; extent:6
Angewandte Chemie / International edition. International edition ; (25.11.2024) (gesamt 6)
- Creator
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Mrozowicz, Michał
Chatterjee, Sagnik
Aliki Mermigki, Markella
Pantazis, Dimitrios A.
Ritter, Tobias
- DOI
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10.1002/anie.202419472
- URN
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urn:nbn:de:101:1-2411261315167.896559888902
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:26 AM CEST
Data provider
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Mrozowicz, Michał
- Chatterjee, Sagnik
- Aliki Mermigki, Markella
- Pantazis, Dimitrios A.
- Ritter, Tobias
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