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Alkylation and acylation of 2-aminopyrimidine N-oxides Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 1981, Volume: 17, Number: 11, Pages: 1105-1112 Pages count : 8 DOI: 10.1007/BF00506462
Authors Sedova V.F. 1 , Mustafina T.Yu. 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: Products of both O- and N-acylation are formed in the acylation of 2-aminopyrimidine N-oxides, whereas only O-alkylation products are formed by the action of alkylating agents. The reaction of 2-aminopyrimidine N-oxides with aldehydes gives only products of reaction at the amino group; the structures of the resulting compounds depend on the reactivity of the carbonyl component. © 1982 Plenum Publishing Corporation.
Cite: Sedova V.F. , Mustafina T.Y. , Mamaev V.P.
Alkylation and acylation of 2-aminopyrimidine N-oxides
Chemistry of Heterocyclic Compounds. 1981. V.17. N11. P.1105-1112. DOI: 10.1007/BF00506462 Scopus РИНЦ OpenAlex
Original: Sedova V.F. , Mustafina T.Y. , Mamayev V.P.
ALKYLATION AND ACYLATION OF 2-AMINOPYRIDINE N-OXIDES
Химия гетероциклических соединений/Khimiya Geterotsiklicheskikh Soedinenii. 1981. N11. P.1515-1522. WOS
Dates:
Published print: Nov 1, 1981
Identifiers:
Scopus: 2-s2.0-34250231023
Elibrary: 30981720
OpenAlex: W2050368833
Citing:
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Scopus 2
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