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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.date.accessioned2018-10-10T12:42:12Z-
dc.date.available2018-10-10T12:42:12Z-
dc.date.issued2016-
dc.identifier.citationOstrovskii, V.A., Mazur, M.S., Mikhailenko, V.V., Aksenov, N.A., Aksenov, A.V. Introduction of tetrazol-1-yl and 5-methyltetrazol-1-yl substituents in the phenyl ring of dibenzo-18-crown-6 // Chemistry of Heterocyclic Compounds. - 2016. - Volume 52. - Issue 10. - Pages 849-851ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/3184-
dc.description.abstractDerivatives of the macrocyclic polyether dibenzo-18-crown-6 containing tetrazol-1-yl and 5-methyltetrazol-1-yl substituents in one of the phenyl rings have been synthesized for the first time: 1-(6,7,9,10,17,18,20,21-octahydrodibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecen- 2-yl)-1H-tetrazole and 5-methyl-1-(6,7,9,10,17,18,20,21-octahydrodibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecen- 2-yl)-1H-tetrazole, respectively. The first compound was obtained by a three-component domino reaction involving an arylamino derivative of dibenzo-18-crown-6, triethyl orthoformate, and sodium azide in glacial acetic acid. The second compound was prepared by treating the appropriate acetamide with tetrachlorosilane–sodium azide system in acetonitrileru
dc.language.isoenru
dc.publisherSpringer New York LLCru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subjectTetrazol-1-ylru
dc.subject5-methyltetrazol-1-ylru
dc.subjectDibenzo-18-crown-6ru
dc.titleIntroduction of tetrazol-1-yl and 5-methyltetrazol-1-yl substituents in the phenyl ring of dibenzo-18-crown-6ru
dc.typeСтатьяru
vkr.amountPages 849-851ru
vkr.instИнститут математики и естественных наук-
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