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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3297
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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.authorSkomorokhov, A. A.-
dc.contributor.authorСкоморохов, А. А.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.contributor.authorGriaznov, G. D.-
dc.contributor.authorГрязнов, Г. Д.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2018-10-19T09:58:39Z-
dc.date.available2018-10-19T09:58:39Z-
dc.date.issued2016-
dc.identifier.citationAksenov, A.V., Aksenov, N.A., Skomorokhov, A.A., Aksenova, I.V., Gryaznov, G.D., Voskressensky, L.G., Rubin, M.A. Michael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesis // Chemistry of Heterocyclic Compounds. - 2016. - Volume 52. - Issue 11. - Pages 923-927ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/3297-
dc.description.abstractA novel highly efficient preparative method for the synthesis of substituted indoles using conjugate addition of nucleophiles to 3-(2-nitrovinyl)indoles has been developed. The addition of nucleophiles generated in the presence of a base from CH acids was investigated. The studied reactions proceed quickly and smoothly under the conditions of microwave activation and do not require protection of the indole nitrogen atomru
dc.language.isoenru
dc.publisherSpringer New York LLCru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subjectAdditionru
dc.subjectIndolesru
dc.subjectMichael reactionru
dc.subjectNitroalkenesru
dc.titleMichael addition to unprotected 3-(2-nitrovinyl)indoles under the conditions of microwave synthesisru
dc.typeСтатьяru
vkr.amountPages 923-927ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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