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Trifluoromethylthiolative 1,2-difunctionalization of alkenes with diselenides and AgSCF3
Perumal Saravanan,
Published in Royal Society of Chemistry
2019
PMID: 30932110
Volume: 55
   
Issue: 32
Pages: 4639 - 4642
Abstract
An efficient regioselective difunctionalization of alkenes via trifluoromethylthiolation has been accomplished employing diaryl diselenide and AgSCF3 in the presence of BF3·OEt2. Various substituted 1,2-dichalcogenated products having the SCF3 moiety were synthesized in good to excellent yields under mild conditions. The preliminary mechanistic investigation revealed the possible reaction pathway and unique combination of diselenide and AgSCF3 for successful transformation. © The Royal Society of Chemistry.
About the journal
JournalData powered by TypesetChemical Communications
PublisherData powered by TypesetRoyal Society of Chemistry
ISSN13597345
Open AccessNo
Concepts (14)
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    Alkene derivative
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    Fluoride
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    Organoselenium derivative
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    Scandium
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    SILVER DERIVATIVE
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    Article
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    Catalyst
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    Chemical analysis
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    Chemical modification
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    Chemical reaction
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    Fluorine nuclear magnetic resonance
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    Nucleophilicity
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    Room temperature
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    Synthesis