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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3532
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dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorKhamraev, V. F.-
dc.contributor.authorХамраев, В. Ф.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2018-12-03T13:10:54Z-
dc.date.available2018-12-03T13:10:54Z-
dc.date.issued2018-
dc.identifier.citationAksenov, A.V., Aksenov, N.A., Aksenov, D.A., Khamraev, V.F., Rubin, M. Nitrostyrenes as 1,4-CCNO-dipoles: diastereoselective formal [4+1] cycloaddition of indoles // Chemical communications (Cambridge, England). - 2018. - Volume 54. - Issue 94. - Pages 13260-13263ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/3532-
dc.description.abstractAn unusual reactivity of nitrostyrenes in phosphorous acid was discovered, which permits the employment of these readily available synthons as 1,4-CCNO-dipole surrogates in a highly diastereoselective (4+1)-cycloaddition of indoles to afford 4'H-spiro[indole-3,5'-isoxazoles] in a diastereomerically pure formru
dc.language.isoenru
dc.publisherNLM (Medline)ru
dc.relation.ispartofseriesChemical communications-
dc.subjectIndoleru
dc.subjectCycloaddition of indolesru
dc.titleNitrostyrenes as 1,4-CCNO-dipoles: diastereoselective formal [4+1] cycloaddition of indolesru
dc.typeСтатьяru
vkr.amountPages 13260-13263ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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