A new synthetic approach to functionalized bicyclo[3.2.1]octanes

Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/2929

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DC Field	Value	Language
dc.contributor.author	Dotsenko, V. V.	-
dc.contributor.author	Доценко, В. В.	-
dc.contributor.author	Aksenov, N. A.	-
dc.contributor.author	Аксенов, Н. А.	-
dc.date.accessioned	2018-09-11T08:58:33Z	-
dc.date.available	2018-09-11T08:58:33Z	-
dc.date.issued	2018	-
dc.identifier.citation	Ismiev, A.I., Dotsenko, V.V., Aksenov, N.A., Mamedova, G.Z., Magerramov, A.M. A new synthetic approach to functionalized bicyclo[3.2.1]octanes // Russian Journal of General Chemistry. - 2018. - Volume 88. - Issue 7. - Pages 1533-1536	ru
dc.identifier.uri	http://hdl.handle.net/20.500.12258/2929	-
dc.description.abstract	The reaction of furfural with secondary amines and isopropyl cyanoacetate gave previously unkown diisopropyl esters of 8-(dialkylamino)-6-oxo-3-(2-furyl)-2,4-dicyanobicyclo- [3.2.1]octane-2,4-dicarboxylic acid	ru
dc.language.iso	en	ru
dc.publisher	Pleiades Publishing	ru
dc.relation.ispartofseries	Russian Journal of General Chemistry	-
dc.subject	Bicyclo [3.2.1]octane	ru
dc.subject	Carbocyclization	ru
dc.subject	Furfural	ru
dc.subject	Isopropyl cyanoacetate	ru
dc.subject	Nazarov reaction	ru
dc.subject	Stenhouse salts	ru
dc.title	A new synthetic approach to functionalized bicyclo[3.2.1]octanes	ru
dc.type	Статья	ru
vkr.amount	Pages 1533-1536	ru
vkr.inst	Институт математики и естественных наук	-
Appears in Collections:	Статьи, проиндексированные в SCOPUS, WOS

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