UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

Observations on the alpha-fluorination of alpha-phenylsulfanyl esters using difluoroiodotoluene

Greaney, MF; Motherwell, WB; (2000) Observations on the alpha-fluorination of alpha-phenylsulfanyl esters using difluoroiodotoluene. TETRAHEDRON LETT , 41 (22) 4463 - 4466.

Full text not available from this repository.

Abstract

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.

Type: Article
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 > Chemistry
URI: http://discovery.ucl.ac.uk/id/eprint/145267
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item