Oxidative nucleophilic substitution of hydrogen in nitroarenes with trifluoromethyl carbanions. Synthesis of trifluoromethyl phenols-Science-Chemical Encyclopedia-lookchem

Oxidative nucleophilic substitution of hydrogen in nitroarenes with trifluoromethyl carbanions. Synthesis of trifluoromethyl phenols
Add time:08/08/2019 Source:sciencedirect.com

Trifluoromethyl carbanions generated from the Ruppert reagent and TASF add to highly electron-deficient nitroarenes to produce σH adducts subsequently oxidized with dimethyldioxirane to substituted trifluoromethyl phenols.

We also recommend Trading Suppliers and Manufacturers of 3-Chloro-2-(trifluoromethyl)phenol (cas 106877-34-3). Pls Click Website Link as below: cas 106877-34-3 suppliers

Prev:Intramolecular construction of trifluoromethyl group by the palladium-catalyzed reaction of 2,3,3-trifluoroallylic carbonates with O-nucleophiles
Next: Synthesis, antimicrobial, antioxidant, cytotoxic, antiurease and molecular docking studies of N-(3-trifluoromethyl)benzoyl-N′-aryl thiourea derivatives)

Click to view details

Health and Chemicalmore >