期刊
ORGANIC LETTERS
卷 25, 期 4, 页码 581-586出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c03956
关键词
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A practical electrochemical method for fluorosulfonylation of aryl and alkyl thianthrenium salts without external redox reagents or metal catalysts is presented. This method, in combination with the C-H thianthrenation of aromatics, provides a new tool for site-selective fluorosulfonylation of drugs.
A practical electrochemically driven method for fluorosul-fonylation of both aryl and alkyl thianthrenium salts has been disclosed. The strategy does not need external redox reagents or metal catalysts. In combination with C-H thianthrenation of aromatics, this method provides a new tool for the site-selective fluorosulfonylation of drugs.
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