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Synthesis and properties of phenyl(methyl)-substituted 2- and 4-nitrosopyrimidines Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 1989, Volume: 25, Number: 7, Pages: 805-811 Pages count : 7 DOI: 10.1007/BF00472754
Authors Moskalenko G.G. 1 , Sedova V.F. 1 , Mamaev V.P. 1
Affiliations
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

Abstract: Phenyl(methyl)-substituted 2- and 4-nitroso- and azoxypyrimidines were synthesized for the first time by the oxidation of phenyl(methyl)-substituted 2- and 4-hydroxy-aminopyrimidines by activated MnO2, Ag2CO3 on zeolite, or BaMnO4. Certain chemical properties of the synthesized nitrosopyrimidines were studied, such as reduction, nucleophilic substitution of the nitroso group, the condensation reaction with aniline and hydroxyaminopyrimidines. © 1990 Plenum Publishing Corporation.
Cite: Moskalenko G.G. , Sedova V.F. , Mamaev V.P.
Synthesis and properties of phenyl(methyl)-substituted 2- and 4-nitrosopyrimidines
Chemistry of Heterocyclic Compounds. 1989. V.25. N7. P.805-811. DOI: 10.1007/BF00472754 Scopus РИНЦ OpenAlex
Dates:
Published print: Jul 1, 1989
Identifiers:
Scopus: 2-s2.0-34249953524
Elibrary: 30979526
OpenAlex: W2059261878
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