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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/14636
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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.accessioned2020-11-25T09:05:10Z-
dc.date.available2020-11-25T09:05:10Z-
dc.date.issued2020-
dc.identifier.citationIsmiyev, A.I., Dotsenko, V.V., Aksenov, N.A., Aksenova, I.V., Magerramov, A.M. Synthesis and structure of new 2,4-dicyano-6-oxo-3-phenylbicyclo[3.2.1]octane-2,4-dicarboxylates // Russian Chemical Bulletin. - 2020. - Volume 69. - Issue 10. - Pages 1938-1943ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/14636-
dc.description.abstractThe sequential reaction of furfural with cyclic secondary amines and further with benzaldehyde and cyanoacetates affords new 2,4-dicyano-8-(R2N)-6-oxo-3-phenylbicyclo[3.2.1]-octane-2,4-dicarboxylates as rac-(1R,2R,3R,4S,5S,8R)-diastereomers. The structures of the reaction products were determined by X-ray diffractionru
dc.language.isoenru
dc.publisherSpringerru
dc.relation.ispartofseriesRussian Chemical Bulletin-
dc.subjectAza-Piancatelli rearrangementru
dc.subjectBicyclo[3.2.1]octaneru
dc.subjectCyanoacetatesru
dc.subjectFurfuralru
dc.subjectNazarov reactionru
dc.subjectStenhouse saltsru
dc.subjectX-ray analysisru
dc.titleSynthesis and structure of new 2,4-dicyano-6-oxo-3-phenylbicyclo[3.2.1]octane-2,4-dicarboxylatesru
dc.typeСтатьяru
vkr.instИнститут математики и естественных наукru
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