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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/539
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dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2018-06-08T12:58:15Z-
dc.date.available2018-06-08T12:58:15Z-
dc.date.issued2017-
dc.identifier.citationDubovtsev, A.Yu., Dmitriev, M.V., Maslivets, A.N., Rubin, M. Regiodivergent condensation of 5-alkoxycarbonyl-1H-pyrrol-2, 3-diones with cyclic ketazinones en route to spirocyclic scaffolds // Beilstein Journal of Organic Chemistry. - 2017. - Volume 13. - pp. 2179-2185.ru
dc.identifier.urihttps://www.scopus.com/record/display.uri?eid=2-s2.0-85033587113&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=nort*+caucas*+fed*+univ*&sid=d5d8a0d301244722be90437f5b553481&sot=afnl&sdt=cl&cluster=scopubyr%2c%222017%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=21&citeCnt=0&searchTerm=-
dc.identifier.urihttps://dspace.ncfu.ru:443/handle/20.500.12258/539-
dc.description.abstractThe condensation of 5-alkoxycarbonyl-1H-pyrrolediones with cyclic ketazinones was systematically investigated. It was discovered that the regioselectivity of this reaction can be easily swapped between two alternative directions affording derivatives of partially hydrogenated indole or benzofurane. The control of this regioselectivity is efficiently governed by steric effects at the hydrazone moiety of the ketazinone reagentru
dc.language.isoenru
dc.publisherBeilstein-Institut Zur Forderung der Chemischen Wissenschaftenru
dc.relation.ispartofseriesBeilstein Journal of Organic Chemistry-
dc.subjectNitrogen heterocyclesru
dc.subjectOxygen heterocyclesru
dc.subjectPyrroledionesru
dc.subjectSpiro compoundsru
dc.subjectSynthetic methodsru
dc.titleRegiodivergent condensation of 5-alkoxycarbonyl-1H-pyrrol-2, 3-diones with cyclic ketazinones en route to spirocyclic scaffoldsru
dc.typeСтатьяru
vkr.amountPages 2179-2185ru
vkr.instИнститут математики и естественных наук-
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