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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/14299
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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorArutiunov, N. A.-
dc.contributor.authorАрутюнов, Н. А.-
dc.contributor.authorKirilov, N. K.-
dc.contributor.authorКирилов, Н. К.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2020-10-07T12:39:02Z-
dc.date.available2020-10-07T12:39:02Z-
dc.date.issued2020-
dc.identifier.citationAksenov, N.A., Arutiunov, N.A., Kirillov, N.K., Aksenov, D.A., Aksenov, A.V., Rubin, M. Preparation of 1,3,4-oxadiazoles and 1,3,4-thiadiazoles via chemoselective сyclocondensation of electrophilically activated nitroalkanes to (thio)semicarbazides or thiohydrazides // Chemistry of Heterocyclic Compounds. - 2020. - Volume 56. - Issue 8. - Pages 1067-1072ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/14299-
dc.description.abstractUnusual reaction proceeding via the electrophilic activation of nitroalkanes in the presence of polyphosphoric acid has been discovered. Subsequent nucleophilic attack with semicarbazides or thiosemicarbazides allows to access 2-amino-1,3,4-oxadiazoles and 2-amino-1,3,4-thiadiazoles, respectivelyru
dc.language.isoenru
dc.publisherSpringerru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subject1,3,4-oxadiazolesru
dc.subject1,3,4-thiadiazolesru
dc.subjectBronsted acid catalysisru
dc.subjectCascade reactionru
dc.subjectNitroalkanesru
dc.subjectNucleophilic cycloaditionru
dc.subjectSemicarbazidesru
dc.subjectThiosemicarbazidesru
dc.titlePreparation of 1,3,4-oxadiazoles and 1,3,4-thiadiazoles via chemoselective сyclocondensation of electrophilically activated nitroalkanes to (thio)semicarbazides or thiohydrazidesru
dc.typeСтатьяru
vkr.instИнститут математики и естественных наукru
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