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Selective Anodic Fluorination of Heterocyclic Compounds
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Toshio Fuchigami, Toshiki Tajima
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Y. HOU, S. HIGASHIYA, T. FUCHIGAMI
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Mechanism of anodic fluorination
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Novak, Mihaly, Boa, J., Jeka, J.
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Various 2-oxazolidinones were galvanostatically electrooxidized in the presence of various fluoride salts. It was found that a fluorine atom was introduced to the α-position of the nitrogen atom of N-acyl- and N-alkoxycarbonyl-2-oxazolidinones to provide the corresponding α-fluorinated products in moderate to good yields.
Yi Cao +3 more
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Electrochemical fluorination at high anodic potentials
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1971I N Rozhkov, Rozhkov I N
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Anodic films on fluorine anodes: the nature of fluorine overvoltage
Electrochimica Acta, 1987Abstract Polycarbonfluoride films formed on vitreous carbon and pyrolytic graphite anodes in a KF.2HF electrolyte have been studied by in situ cyclic voltammetry and interfacial impedance and ex situ surface spectroscopic and electrochemical kinetic techniques.
O.R. Brown, B.M. Ikeda, M.J. Wilmott
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ChemInform Abstract: Anodic Films on Fluorine Anodes: the Nature of Fluorine Overvoltage.
ChemInform, 1987AbstractPolycarbonfluoride films on carbon anodes in molten KF·2 HF have been studied by in situ voltammetry and interfacial impedance, ex situ surface spectroscopic, and electrochemical techniques.
O. R. BROWN, B. M. IKEDA, M. J. WILMOTT
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Anodic fluorination of azobenzene
Russian Journal of Electrochemistry, 2009Electrolysis of azobenzene (I) in the system of Et4NF · 3HF, MeCN results in predominant fluorination of the products of polymerization of I formed in the course of electrolysis. Also, m-fluoroazobenzene (II) and o-fluoroazobenzene (III) (II: III = 4: 1) were obtained with a low yield.
N. D. Kagramanov +2 more
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