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.
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Mrozowicz, M., Chatterjee, S., Aliki Mermigki, M., Pantazis, D. A., & Ritter, T. (2025). Meta-Dimethylation of Arenes via Catellani Reaction from Aryl Thianthrenium Salts. Angewandte Chemie - International Edition, 64(5). https://doi.org/10.1002/anie.202419472
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