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.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.202419472 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!