Perfluoroalkyl-chalcogenation of olefins has been performed by the reaction of chalcogenide anions with perfluoroalkylhalides (IV-X) in the presence of olefins. Chalcogenide anion cleaves reductively the carbon-halogen bond of Bf-X, generating perfluoroalkyl radicals which undergo addition to C=C bo
โฆ LIBER โฆ
Perfluoroalkyl-selenation of olefins
โ Scribed by Kenji Uneyama; Kouichi Kitagawa; Kouichi Kitagawa
- Book ID
- 104225408
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 223 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Perfluoroalkyl-selenation of olefins has been performed by the reaction of diphenyl diselenide with sodium borohydride followed with perfluoroalkyl halides (RfX) and olefins where one electron transfer from phenylseleno anion to RfX occurs, generating perfluoroalkyl and phenylseleno radicals.
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