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Three-component condensation of 2-aminothiophene-3-carboxylic acid derivatives with aldehydes and Meldrum’s acid Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 2008, Volume: 57, Number: 10, Pages: 2175-2179 Pages count : 5 DOI: 10.1007/s11172-008-0295-1
Authors Lichitsky B.V. 1 , Komogortsev A.N. 1 , Dudinov A.A. 1 , Krayushkin M.M. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

Abstract: New approach to the synthesis of 4,7-dihydro-5H-thieno[2,3-b]pyridin-6-ones using 2-aminothiophenes unsubstituted at position 3 of the thiophene ring has been developed. Labile 2-aminothiophenes have been obtained by the in situ decarboxylation of unstable 2-amino-3-thiophenecarboxylic acids. The three-component condensation of 2-aminothiophenes with aromatic aldehydes and the Meldrum’s acid is the key step of the process.
Cite: Lichitsky B.V. , Komogortsev A.N. , Dudinov A.A. , Krayushkin M.M.
Three-component condensation of 2-aminothiophene-3-carboxylic acid derivatives with aldehydes and Meldrum’s acid
Russian Chemical Bulletin. 2008. V.57. N10. P.2175-2179. DOI: 10.1007/s11172-008-0295-1 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000270586500019
Scopus: 2-s2.0-76449095481
OpenAlex: W1970319761
Citing:
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OpenAlex 8
Scopus 8
Web of science 9
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