Affiliation:
1. College of Chemistry and Life Sciences, Zhejiang Normal University
2. College of Physical Education and Health Sciences, Zhejiang Normal University
Abstract
AbstractWe report a simple protocol for (ethoxycarbonyl)difluoromethylthiolation of nucleophilic compounds using a difluoroalkyl sulfonium salt which can be prepared in situ via Tf2O-triggered electrophilic activation of a benzyl difluoroalkyl sulfoxide. With the protocol, difluoroalkylthiolated arenes, heteroarenes, α-difluoroalkylthiolated carbonyl compounds, etc. were obtained smoothly with good to excellent yields. Merits of the reaction include the readily available difluoroalkylthiolation reagent and substrates, mild conditions, and excellent regioselectivity.
Funder
Zhejiang Normal University
Cited by
3 articles.
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