Copper-mediated direct thiolation of aryl C–H bonds with disulfides?
Organic & Biomolecular Chemistry Pub Date: 2019-07-15 DOI: 10.1039/C9OB01255A
Abstract
An efficient copper-mediated ortho-C(sp2)–H thiolation of aromatic amides directed by a novel directing group [4-chloro-2-(1H-pyrazol-1-yl)phenyl]amine has been developed without the need of other additives or oxidants, allowing for an increased usefulness. With the high compatibility of sterically demanding substrates, this reaction is scalable and can tolerate a wide scope of functional groups to provide alkyl and aryl thioethers in good to excellent yields (up to 93%). Furthermore, the protocol has been successfully implemented for the selenylation as well.
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Journal Name：Organic & Biomolecular Chemistry
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CAS no.: 89640-58-4
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