Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3184
Title: Introduction of tetrazol-1-yl and 5-methyltetrazol-1-yl substituents in the phenyl ring of dibenzo-18-crown-6
Authors: Aksenov, N. A.
Аксенов, Н. А.
Aksenov, A. V.
Аксенов, А. В.
Keywords: Tetrazol-1-yl;5-methyltetrazol-1-yl;Dibenzo-18-crown-6
Issue Date: 2016
Publisher: Springer New York LLC
Citation: Ostrovskii, 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 849-851
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: Derivatives 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 acetonitrile
URI: http://hdl.handle.net/20.500.12258/3184
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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