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Action of vanadium and antimony pentafluorides on polyfluorinated derivatives of cyclohexadinene

Journal Article · · J. Org. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:5950505
Polyfluorinated 1,3- and 1,4-cyclohexadienes are fluorinated by vanadium fluoride at /minus/25 to +25/degree/C. The olefinic fragments of perfluoro-1,3- and perfluoro-1,4-cyclohexadienes are close to each other in reactivity. Under the influence of vanadium pentafluoride the fluorine atoms add to 1-R-haptafluoro-1,4-cyclohexadienes preferentially at the multiple bond containing the less electron-withdrawing substituent. At /minus/80 to +20/degree/C antimony pentafluoride leads to isomerization of the polyfluorinated derivatives of cyclohexadiene.
Research Organization:
Novosibrisk Institute of Organic Chemistry (USSR)
OSTI ID:
5950505
Journal Information:
J. Org. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Org. Chem. USSR (Engl. Transl.); (United States) Vol. 24:7; ISSN JOCYA
Country of Publication:
United States
Language:
English

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