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Please use this identifier to cite or link to this item: https://elib.bsu.by/handle/123456789/197418
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dc.contributor.authorКовганко, Владимир Николаевич-
dc.contributor.authorСтанишевский, Леонид Станиславович-
dc.date.accessioned2018-06-07T12:58:31Z-
dc.date.available2018-06-07T12:58:31Z-
dc.date.issued2002-
dc.identifier.citationВестник Белорусского государственного университета. Сер. 2, Химия. Биология. География. – 2002. - № 3. – С. 15-17.ru
dc.identifier.issn0372-5340-
dc.identifier.urihttp://elib.bsu.by/handle/123456789/197418-
dc.description.abstractA convenient approach to 3,3-dimethyl-4-nitro-5-arylcyclohexanones has been firstly developed. This method involved trifluoroacetic acid catalysed condensation of 5-nitro-4,4-dimethylpentan-2-one with azomethynes to corresponding unsaturated nitroketones and following intramolecular cyclization of these compounds to necessary cyclohexanones.ru
dc.language.isoruru
dc.publisherМинск : БГУru
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.subjectЭБ БГУ::ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Химияru
dc.titleАзометины в синтезе 3,3-диметил-4-нитро-5-арилциклогексаноновru
dc.typearticleru
Appears in Collections:2002, №3 (октябрь)

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