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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3722
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dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorSmirnov, A. N.-
dc.contributor.authorСмирнов, А. Н.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorBijieva, A. S.-
dc.contributor.authorБиджиева, А. С.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2018-12-19T14:16:50Z-
dc.date.available2018-12-19T14:16:50Z-
dc.date.issued2015-
dc.identifier.citationAksenov, A.V., Smirnov, A.N., Aksenov, N.A., Bijieva, A.S., Aksenova, I.V., Rubin, M. Benzimidazoles and benzoxazoles via the nucleophilic addition of anilines to nitroalkanes // Organic and Biomolecular Chemistry. - 2015. - Volume 13. - Issue 14. - Pages 4289-4295ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/3722-
dc.description.abstractPPA-induced umpolung triggers efficient nucleophilic addition of unactivated anilines to nitroalkanes to produce N-hydroxyimidamides. The latter undergo sequential acid-promoted cyclocondensation with ortho-OH or ortho-NHR moieties to afford benzoxazoles and benzimidazoles, respectivelyru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesOrganic and Biomolecular Chemistry-
dc.subjectAddition reactionru
dc.subjectAnilineru
dc.subjectBenzimidazoleru
dc.subjectBenzoxazolesru
dc.subjectCyclocondensationru
dc.subjectNitroalkanesru
dc.subjectNucleophilic additionru
dc.subjectUmpolungru
dc.titleBenzimidazoles and benzoxazoles via the nucleophilic addition of anilines to nitroalkanesru
dc.typeСтатьяru
vkr.amountPages 4289-4295ru
vkr.biblИнститут математики и естественных наук-
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