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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/11431
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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorGasanova, A. Z.-
dc.contributor.authorГасанова, А. З.-
dc.contributor.authorProkonov, F. Y.-
dc.contributor.authorПроконов, Ф. Ю.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.date.accessioned2020-02-18T12:11:26Z-
dc.date.available2020-02-18T12:11:26Z-
dc.date.issued2019-
dc.identifier.citationAksenov, N.A., Gasanova, A.Z., Prokonov, F.Y., Aksenov, D.A., Abakarov, G.M., Aksenov, A.V. Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes // Russian Chemical Bulletin. - 2019. - Volume 68. - Issue 12. - Pages 2262-2270ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/11431-
dc.description.abstractA new method for synthesizing 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed intramolecular electrophilic amination of 2-arylindole-3-carbaldehyde O-acetyl oximes was developedru
dc.language.isoenru
dc.publisherSpringerru
dc.relation.ispartofseriesRussian Chemical Bulletin-
dc.subjectAlkaloidsru
dc.subjectAminationru
dc.subjectIndoloquinolinesru
dc.subjectQuinolineru
dc.titleSynthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximesru
dc.typeСтатьяru
vkr.amountPages 2262-2270ru
vkr.instИнститут математики и естественных наукru
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