1967
DOI: 10.1007/bf00912428
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Structure and reactivity of nitrogen-containing derivatives of carbonyl compounds

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1970
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“…Immonium salts, III, yielded a oneelectron reduction wave in acetonitrile III or dimethylformamide which leads to formation of a free radical (8). The re-duction mechanism for the azomethine group was shown to be dependent on the type of substituents present and the pH of the solution (263).…”
Section: Compoundsmentioning
confidence: 99%
“…Immonium salts, III, yielded a oneelectron reduction wave in acetonitrile III or dimethylformamide which leads to formation of a free radical (8). The re-duction mechanism for the azomethine group was shown to be dependent on the type of substituents present and the pH of the solution (263).…”
Section: Compoundsmentioning
confidence: 99%