Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/693
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.accessioned2018-06-22T09:41:48Z-
dc.date.available2018-06-22T09:41:48Z-
dc.date.issued2017-
dc.identifier.citationKhrustaleva, A.N., Frolov, K.A., Dotsenko, V.V., Aksenov, N.A., Aksenova, I.V., Krivokolysko, S.G. Aminomethylation of Guareschi imides: synthesis of 2,4-dioxo-1H,5H-3,7-spiro[diazabicyclo[3.3.1]nonane-9,4'-piperidine]-1,5-dicarbonitriles // Chemistry of Heterocyclic Compounds. - 2017. - Volume 53. - Issue 8. - pp. 887-891ru
dc.identifier.urihttps://dspace.ncfu.ru:443/handle/20.500.12258/693-
dc.description.abstractThe aminomethylation reaction of 9-benzyl-2,4-dioxo-3,9-diazaspiro[5.5]undecane-1,5-dicarbonitrile hydrochloride in the presence of primary aliphatic amines and an excess of 37% aqueous formaldehyde led to the formation of 7-substituted 1'-benzyl-2,4-dioxo-1H,5Hspiro[3,7-diazabicyclo[3.3.1]nonane-9,4'-piperidine]-1,5-dicarbonitrile derivativesru
dc.language.isoenru
dc.publisherSpringer New York LLCru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subject2,6-Dioxopiperidine-3,5-dicarbonitrilesru
dc.subject3,7-Diazabicyclo[3.3.1]nonanesru
dc.subject3,9-diazaspiro[5.5]undecaneru
dc.subjectAminomethylationru
dc.subjectBispidinesru
dc.subjectGuareschi imidesru
dc.subjectMannich reactionru
dc.titleAminomethylation of Guareschi imides: synthesis of 2,4-dioxo-1H,5H-3,7-spiro[diazabicyclo[3.3.1]nonane-9,4'-piperidine]-1,5-dicarbonitrilesru
dc.typeСтатьяru
vkr.amountPages 887-891ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:
File Description SizeFormat 
scopusresults (112).pdf
  Restricted Access
61.64 kBAdobe PDFView/Open
WoS 65 .pdf
  Restricted Access
79.16 kBAdobe PDFView/Open


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