Reaction of 2,4,6-substituted pyrylium salts with compounds containing a C = N bond |
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Authors: | G. N. Dorofeenko é. A. Zvezdina M. P. Zhdanova V. V. Derbenev E. S. Matskovskaya |
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Affiliation: | 1. Rostov State University, Scientific-Research Institute of Physical and Organic Chemistry, Rostovon-Don
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Abstract: | 2,4,6-Substituted pyrylium salts add azomethines to give pyridinium salts and aromatic aldehydes. The latter can be condensed with the methyl groups of the pyridinium salts. Benzaldoxime, benzalazine, benzalphenylhydrazine, urea, thiourea, and phenyl isothiocyanate react with 2,4,6-triphenylpyrylium perchlorate similarly to give, respectively, 2,4,6-triphenylpyridine N-oxide, 2,4,6-triphenylpyridine, or N-substituted 2,4,6-triphenylpyridinium perchlorates. |
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