Tetrazoles. 42. 2-4(Nitrophenyl)-5-functionally-substituted tetrazoles

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dc.contributor.authorKharbash, Raisako
dc.contributor.authorAlam, LVko
dc.contributor.authorKoreneva, APko
dc.contributor.authorKoldobskii, GIko
dc.date.accessioned2017-03-31T05:44:16Z-
dc.date.available2017-03-31T05:44:16Z-
dc.date.created2017-03-24-
dc.date.created2017-03-24-
dc.date.issued2001-12-
dc.identifier.citationChemistry of Heterocyclic Compounds, v.37, no.12, pp.1493 - 1497-
dc.identifier.issn0009-3122-
dc.identifier.urihttp://hdl.handle.net/10203/222925-
dc.description.abstractWe have studied the reactions of 5-methylsulfonyl-2-(4-nitrophenyl)tetrazole with N- and O-nucleophiles. For the first time we show that in 2-(4-nitrophenyl)-5-phenoxytetrazole, the tetrazole ring is substituted when treated with phenoxide ion, 4-nitrodiphenyl ether being formed.-
dc.languageEnglish-
dc.publisherSPRINGER-
dc.titleTetrazoles. 42. 2-4(Nitrophenyl)-5-functionally-substituted tetrazoles-
dc.typeArticle-
dc.identifier.scopusid2-s2.0-0035751655-
dc.type.rimsART-
dc.citation.volume37-
dc.citation.issue12-
dc.citation.beginningpage1493-
dc.citation.endingpage1497-
dc.citation.publicationnameChemistry of Heterocyclic Compounds-
dc.contributor.nonIdAuthorAlam, LV-
dc.contributor.nonIdAuthorKoreneva, AP-
dc.contributor.nonIdAuthorKoldobskii, GI-
dc.description.isOpenAccessN-
dc.subject.keywordAuthor2, 5-disubstituted tetrazoles-
dc.subject.keywordAuthor5-methylsulfonyl-2-(4-nitrophenyl)tetrazole-
dc.subject.keywordAuthorNucleophilic substitution-
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