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
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
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
Mrozowicz, Michał
Chatterjee, Sagnik
Aliki Mermigki, Markella
Pantazis, Dimitrios A.
Ritter, Tobias

DOI
10.1002/anie.202419472
URN
urn:nbn:de:101:1-2411261315167.896559888902
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:26 AM CEST

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Associated

  • Mrozowicz, Michał
  • Chatterjee, Sagnik
  • Aliki Mermigki, Markella
  • Pantazis, Dimitrios A.
  • Ritter, Tobias

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