Observations on the alpha-fluorination of alpha-phenylsulfanyl esters using difluoroiodotoluene.
4463 - 4466.
alpha-Phenylsulfanyl esters are fluorinated in the alpha-position when treated with the hypervalent iodine reagent difluoroiodotoluene. Excess reagent can lead to alpha-fluoro sulfoxides, which can then undergo thermal syn elimination to produce vinyl fluorides. (C) 2000 Elsevier Science Ltd. All rights reserved.
|Title:||Observations on the alpha-fluorination of alpha-phenylsulfanyl esters using difluoroiodotoluene|
|Keywords:||halogenation, hypervalent elements, fluorine and compounds, FLUORO THIOETHERS, (DIETHYLAMINO)SULFUR TRIFLUORIDE, OXIDATIVE-FLUORINATION, ANTIMONY(III) CHLORIDE, XENON DIFLUORIDE, SULFIDES, ANALOGS, 4-METHYL(DIFLUOROIODO)BENZENE, CONVERSION, SULFOXIDES|
|UCL classification:||UCL > School of BEAMS > Faculty of Maths and Physical Sciences
UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry
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