Electrochemically induced reactions of some halogenated organic compounds (Part I) ; Novel rearrangements of pyridazine derivatives (Part II)
The reduction of pentafluoropyridine gave, as the major products, octafluoro-4,4'-bipyridyl in aprotic systems and 4-H-tetrafluoropyridine with added proton donor. Garbanionic intermediates were not trapped by carbon dioxide to give acids. Voltammetric results for a series of polyfluoropyridine...
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Durham University
1978
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.348059 |