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Synthesis of acetonylmalonaldehyde and its interaction with aminoazoles Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 1997, Volume: 46, Number: 6, Pages: 1178-1179 Pages count : 2 DOI: 10.1007/bf02496225
Authors Vartanyan M.M. 1 , Eliseev O.L. 1 , Skov Kh.R. 2 , Karakhanov R.A. 3
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, Moscow, Russian Federation
2 Hexagon Company, Copenhagen, Denmark
3 I. M. Gubkin State Academy of Oil and Gas, 65 Leninsky prosp., 117917, Moscow, Russian Federation

Abstract: Acetonylmalonaldehyde (1) was obtained for the first time by hydrolysis of 2,5-dimethoxy-5-methyltetrahydrofuran-3-carbaldehyde. The interaction of1 with 3-amino-5-methylpyrazole, 3-amino-1,2,4-triazole, 2-aminobenzimidazole, and 5-aminotetrazole results in the formation of functionally substituted azolopyrimidines.
Cite: Vartanyan M.M. , Eliseev O.L. , Skov K.R. , Karakhanov R.A.
Synthesis of acetonylmalonaldehyde and its interaction with aminoazoles
Russian Chemical Bulletin. 1997. V.46. N6. P.1178-1179. DOI: 10.1007/bf02496225 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:A1997YC26700029
Scopus: 2-s2.0-0031517242
OpenAlex: W2949470982
Citing:
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OpenAlex 5
Scopus 5
Web of science 5
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