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Reaction of aryl-substituted azidopyrimidines with 1,3-dicarbonyl compounds Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 1983, Volume: 19, Number: 10, Pages: 1116-1120 Pages count : 5 DOI: 10.1007/BF00505770
Authors Krivopalov V.P. 1,2 , Nikolaenkova E.B. 1,2 , Sedova V.F. 1,2 , Mamaev V.P. 1,2
Affiliations
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR
2 (Scopus) Novosibirsk Branch, All-Union Scientific-Research Institute of Chemical Agents for the Protection of Plants, at the Novosibirsk Institute of Organic Chemistry

Abstract: Substituted 1-pyrimidyl-4-acyl-1,2,3-triazoles were obtained by the reaction of 2- and 4-azidopyrimidines with aryl substituents with acetyl- or benzoylacetone. An accelerating effect of an o-hydroxyphenylpyrimidine fragment in this reaction, which was explained by the effect of an intramolecular hydrogen bond, was observed. © 1984 Plenum Publishing Corporation.
Cite: Krivopalov V.P. , Nikolaenkova E.B. , Sedova V.F. , Mamaev V.P.
Reaction of aryl-substituted azidopyrimidines with 1,3-dicarbonyl compounds
Chemistry of Heterocyclic Compounds. 1983. V.19. N10. P.1116-1120. DOI: 10.1007/BF00505770 Scopus РИНЦ OpenAlex
Dates:
Published print: Oct 1, 1983
Identifiers:
Scopus: 2-s2.0-34250138168
Elibrary: 30919580
OpenAlex: W2076911458
Citing:
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Scopus 4
Elibrary 4
OpenAlex 4
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