Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 40, Pages 5993-5995Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b913962a
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Funding
- ETH Zurich
- Stipendienfonds der Schweizerischen Chemischen Industrie
- French-Swiss Germaine de Stae programme
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A variety of sulfonic acids have been trifluoromethylated using 1-trifluoromethyl- 1,2-benziodoxol-3(1H)-one under mild conditions in good to excellent yields. Initial mechanistic investigations of this reaction show a clean second-order kinetics and only very weak substrate electronic effects.
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