Three-component condensation of 2,4-diaminothiazoles with aldehydes and Meldrum's acid: synthesis of 7-aryl(alkyl)-substituted 6,7-dihydro-4H-thiazolo[4,5-b]pyridin-5-ones Full article
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Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436 |
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| Output data | Year: 2009, Volume: 19, Number: 2, Pages: 87-88 Pages count : 2 DOI: 10.1016/j.mencom.2009.03.011 | ||
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Abstract:
The new method of the synthesis of 6,7-dihydro-4H-thiazolo[4,5-b]pyridin-5-ones, based on decarboxylation of corresponding 2,4-diamino-5-thiazolecarboxylic acids has been elaborated; unstable derivatives of 2,4-diaminothiazole, generated in situ as a result of decarboxylation, react with aldehydes and Meldrum's acid forming target compounds.
Cite:
Dudinov A.A.
, Lichitsky B.V.
, Komogortsev A.N.
, Krayushkin M.M.
Three-component condensation of 2,4-diaminothiazoles with aldehydes and Meldrum's acid: synthesis of 7-aryl(alkyl)-substituted 6,7-dihydro-4H-thiazolo[4,5-b]pyridin-5-ones
Mendeleev Communications. 2009. V.19. N2. P.87-88. DOI: 10.1016/j.mencom.2009.03.011 WOS Scopus OpenAlex
Three-component condensation of 2,4-diaminothiazoles with aldehydes and Meldrum's acid: synthesis of 7-aryl(alkyl)-substituted 6,7-dihydro-4H-thiazolo[4,5-b]pyridin-5-ones
Mendeleev Communications. 2009. V.19. N2. P.87-88. DOI: 10.1016/j.mencom.2009.03.011 WOS Scopus OpenAlex
Identifiers:
| Web of science: | WOS:000265870700011 |
| Scopus: | 2-s2.0-63749105891 |
| OpenAlex: | W2951833383 |