In water multicomponent synthesis of low-molecular-mass 4,7-dihydrotetrazolo[1,5-a]pyrimidines

dc.contributor.authorTkachenko, I. G.
dc.contributor.authorKomykhov, S. A.
dc.contributor.authorMusatov, V. I.
dc.contributor.authorShishkina, S. V.
dc.contributor.authorDyakonenko, V. V.
dc.contributor.authorShvets, V. N.
dc.contributor.authorDiachkov, M. V.
dc.contributor.authorChebanov, V. A.
dc.contributor.authorDesenko, S. M.
dc.contributor.authorШвець, Володимир Миколайович
dc.date.accessioned2022-01-17T11:09:40Z
dc.date.available2022-01-17T11:09:40Z
dc.date.issued2019
dc.description.abstractThe three-component reaction of 5-aminotetrazole with aliphatic aldehydes (formaldehyde, acetaldehyde) and acetoacetic ester derivatives in water under microwave irradiation leads to the selective formation of 4,7-dihydrotetrazolo[1,5-a]pyrimidine derivatives. Under similar conditions using 4,4,4-trifluoroacetoacetic ester 5-hydroxy-4,5,6,7-tetrahydrotetrazolo[1,5-a]pyrimidines are obtained. The analogous reaction with acetylacetone requires scandium(III) triflate as catalyst. The antioxidant activity of selected compounds was assayed with 1,1-diphenyl-2-picrylhydrazyl.uk_UK
dc.identifier.citationIn water multicomponent synthesis of low-molecular-mass 4,7-dihydrotetrazolo[1,5-a]pyrimidines / I. G. Tkachenko, S. A. Komykhov, V. I. Musatov, S. V. Shishkina, V. V. Dyakonenko, V. N. Shvets, M. V. Diachkov, V. A. Chebanov, S. M. Desenko // Beilstein Journal of Organic Chemistry. - 2019. - № 15. - P. 2390-2397. - https://doi.org/10.3762/bjoc.15.231.uk_UK
dc.identifier.urihttps://zsmu.rosbai.com/handle/123456789/15930
dc.language.isoenuk_UK
dc.subject5-aminotetrazoleuk_UK
dc.subjectantioxidant activityuk_UK
dc.subject1,3-dicarbonyl compoundsuk_UK
dc.subjectmulticomponent synthesisuk_UK
dc.subjecttetrazolo[1,5-a]pyrimidinesuk_UK
dc.titleIn water multicomponent synthesis of low-molecular-mass 4,7-dihydrotetrazolo[1,5-a]pyrimidinesuk_UK
dc.typeArticleuk_UK

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