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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/14300
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dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.date.accessioned2020-10-07T13:39:53Z-
dc.date.available2020-10-07T13:39:53Z-
dc.date.issued2020-
dc.identifier.citationPlieva, A.T., Chalikidi, P.N., Gutnov, A.V., Turiev, A.M., Demidov, O.P., Aksenov, N.A., Magkoev, T.T., Abaev, V.T. Novel synthetic approach to pyrrolo[1,2-b]cinnolines // Chemistry of Heterocyclic Compounds. - 2020. - Volume 56. - Issue 8. - Pages 1030-1041ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/14300-
dc.description.abstractStraightforward method for the synthesis of pyrrolo[1,2-b]cinnolines starting from 2-nitrobenzaldehydes and 2-methylfurans has been elaborated. The key steps of the process are oxidative furan ring opening with diazonium cation and intramolecular alkylation of azo group of the resulted cinnoline with secondary allyl alcoholru
dc.language.isoenru
dc.publisherSpringerru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subjectAza-heterocyclesru
dc.subjectCinnolinesru
dc.subjectFuran ring openingru
dc.subjectPyrrolo[1,2-b]cinnolinesru
dc.titleNovel synthetic approach to pyrrolo[1,2-b]cinnolinesru
dc.typeСтатьяru
vkr.instИнститут математики и естественных наукru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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