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Novel Electrochemically Derived Dimers of Methylated Uracils
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Published/Copyright:
June 2, 2014
Abstract
Electrolysis of acetic acid/sodium acetate solutions of N-methylated uracils results in the formation of 5-substituted methyl and acethoxy derivatives. Electrolysis of trifluoroacetic acid/potassium trifluoroacetate solutions of N-1-and N-3-methylated uracils provided, be sides 5-trifluoromethyl derivatives, novel N-C uracil dimers. In the case of 1,3-dimethyluracil in trifluoroacetic acid. N-l demethylathion was also observed.
Keywords: Electrolysis; Radical Substitution; Uracil Dimers of N-C; Electrochemical Oxidation Electrochemical Trifluoromethylation
Received: 1997-3-6
Published Online: 2014-6-2
Published in Print: 1997-6-1
© 1946 – 2014: Verlag der Zeitschrift für Naturforschung
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Keywords for this article
Electrolysis;
Radical Substitution;
Uracil Dimers of N-C;
Electrochemical Oxidation Electrochemical Trifluoromethylation
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