Please use this identifier to cite or link to this item: https://elib.belstu.by/handle/123456789/21090
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dc.contributor.authorAntonevich, I. P.en
dc.contributor.authorKatok, Ya. M.en
dc.contributor.authorNesterova, S. V.en
dc.date.accessioned2017-06-06T05:30:15Z-
dc.date.available2017-06-06T05:30:15Z-
dc.date.issued2015-
dc.identifier.citationAntonevich, I. P. The interaction of (2-fluorophenyl) and (4-fluorophenyl)-(2-nitomethylcyclopentyl)methanone with phenylacetylene / I. P. Antonevich, Ya. M. Katok, S. V. Nesterova // Proceedings of BSTU. No. 4. – Minsk : BSTU, 2015. – P. 66-71en
dc.identifier.urihttps://elib.belstu.by/handle/123456789/21090-
dc.description.abstractThe synthesis of corresponding isoxazoles and unsaturated oximes has been realized via the 1,3-dipolar cycloaddition reaction of phenylacetylene with nitrile oxide s generated from (2-fluorophenyl)-or (4-fluorophenyl)-(2-nitomethylcyclopentyl)methanone by the action of phenyl isocyanate. The synthesized compounds are new fluorinated prostanoids and appear to be of great interest as potential biologically active substances.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherBSTUen
dc.subjectфторсодержащие простаноидыru
dc.subjectнитросоединенияru
dc.subjectнитрилоксидыru
dc.subjectизоксазолыru
dc.subjectоксимыru
dc.titleThe interaction of (2-fluorophenyl) and (4-fluorophenyl)-(2-nitomethylcyclopentyl)methanone with phenylacetyleneen
dc.typeArticleen
Appears in Collections:2015, № 4

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