Selective reduction of saturated perfluorocarbons

Autor: Anne M. Coughlin, John Anthony Marsella, Andrew G. Gilicinski, Guido Peter Pez
Rok vydání: 1992
Předmět:
Zdroj: The Journal of Organic Chemistry. 57:2856-2860
ISSN: 1520-6904
0022-3263
DOI: 10.1021/jo00036a019
Popis: Perfluorocycloaliphatic compounds are reduced by solutions of the sodium benzophenone radical anion to give perfluorinated and highly fluorinated aromatic compounds. Perfluorocycloalkanes containing tertiary carbon centers are much more reactive than perfluorocyclohexane. Reduction of perfluoroalkanes and perfluorocycloalkanes that contain perfluoroalkyl substituents proceeds easily; however, it appears that overreduction occurs and no organofluorine products are obtained with these substrates
Databáze: OpenAIRE