Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/7502
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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorSkomorokhov, A. A.-
dc.contributor.authorСкоморохов, А. А.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2019-09-25T12:22:39Z-
dc.date.available2019-09-25T12:22:39Z-
dc.date.issued2019-
dc.identifier.citationAksenov, N.A., Skomorokhov, A.A., Aksenov, A.V., Voskressensky, L.G., Rubin, M.A. Michael addition to 3-(2-nitrovinyl)indoles – route toward aliphatic nitro compounds with heterocyclic substituents // Chemistry of Heterocyclic Compounds. - 2019. - Volume 55. - Issue 6. - Pages 541-546ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/7502-
dc.description.abstractSynthetic approach toward indole derivatives bearing 2-nitroethyl group and polar azole moiety has been developed. This method involves conjugate addition of 1,3-dicarbonyl compounds to 3-(2-nitrovinyl)-1H-indoles followed by cyclocondensation with hydrazine or hydroxylamine to furnish pyrazole or isoxazole ring. Application of microwave activation allows to obtain the target indole derivatives in short time and avoid protection of indole nitrogen atomru
dc.language.isoenru
dc.publisherSpringer New York LLCru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subjectIndoleru
dc.subjectIsoxazoleru
dc.subjectMichael additionru
dc.subjectMicrowave-assisted synthesisru
dc.subjectNitroalkenesru
dc.subjectPyrazoleru
dc.titleMichael addition to 3-(2-nitrovinyl)indoles – route toward aliphatic nitro compounds with heterocyclic substituentsru
dc.typeСтатьяru
vkr.amountPages 541-546ru
vkr.instИнститут математики и естественных наук-
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