Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/8339
Full metadata record
DC FieldValueLanguage
dc.contributor.authorDotsenko, V. V.-
dc.contributor.authorДоценко, В. В.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.date.accessioned2019-11-14T08:44:01Z-
dc.date.available2019-11-14T08:44:01Z-
dc.date.issued2019-
dc.identifier.citationDotsenko, V.V., Dushenko, V.A., Aksenov, N.A., Aksenova, I.V., Netreba, E.E. Unexpected Result of Thiophosphorylation of 6-Aminopyrano[2,3-c]pyrazole-5-carbonitrile Derivative // Russian Journal of General Chemistry. - 2019. - Volume 89. - Issue 9. - Pages 1752-1759ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/8339-
dc.description.abstractThe reaction of 6-amino-3-methyl-4-(2,4-dichlorophenyl)-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile with phosphorus sulfide in boiling pyridine unexpectedly leads to the formation of a not previously described heterocyclic system—[1,2]oxaphosphinino[6,5-c]pyrazole derivative. Structure of the obtained compound was proved using 2D NMR spectroscopy and X-ray diffraction analysisru
dc.language.isoenru
dc.publisherPleiades Publishingru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subject1,2-oxaphosphininesru
dc.subjectPhosphorus(V) sulfideru
dc.subjectPyrano[2,3-c]pyrazolesru
dc.subjectThiophosphorylationru
dc.titleUnexpected result of thiophosphorylation of 6-aminopyrano[2,3-c]pyrazole-5-carbonitrile derivativeru
dc.typeСтатьяru
vkr.amountPages 1752-1759ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:
File SizeFormat 
scopusresults 1049 .pdf
  Restricted Access
132.61 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.