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Abstract
The hydrolysis, alcoholysis, and hydrazinolysis of N-phenacylpyridinium bromide lead to the corresponding benzoic acid derivatives. In addition, 3,6-diphenylpyridazine is formed during hydrazinolysis. The hydrolysis and alcoholysis of N-phenacylisoquinolinium bromide lead to its dimerization, whereas hydrazinolysis gives a triazinoisoquinoline derivative.
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