Reaction of β-aminopropionohydroxamic acid with aldehydes and ketones |
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| Authors: | O. A. Luk'yanov P. B. Gordeev |
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| Affiliation: | (1) N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913 Moscow, Russian Federation |
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| Abstract: | β-Aminopropionohydroxamic acid reacts with aliphatic aldehydes or ketones to give 2-substituted 1-hydroxytetrahydropyrimidin-6-ones, while its reaction with aromatic carbonyl compounds leads to either the same products or Schiff's bases, which can exist in tautomeric equilibrium in solution. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 691–694, April, 1998. |
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| Keywords: | β -aminopropionohydroxamic acid 1-hydroxytetrahydropyrimidin-6-ones aldehydes ketones Schiff's bases reaction tautomeric equilibrium |
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