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Полная запись метаданных
Поле DC | Значение | Язык |
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dc.contributor.author | Marquise, N. | - |
dc.contributor.author | ChevallierF., Chevallier F. | - |
dc.contributor.author | Nassar, E. | - |
dc.contributor.author | Frederich, M. | - |
dc.contributor.author | Ledoux, A. | - |
dc.contributor.author | Halauko, Y.S. | - |
dc.contributor.author | Ivashkevich, O.A. | - |
dc.contributor.author | Matulis, V.E. | - |
dc.contributor.author | Roisnel, T. | - |
dc.contributor.author | Dorcet, V. | - |
dc.contributor.author | Mongin, F. | - |
dc.date.accessioned | 2021-08-19T07:29:48Z | - |
dc.date.available | 2021-08-19T07:29:48Z | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | Tetrahedron 2016;72(6):825-836. | ru |
dc.identifier.uri | https://elib.bsu.by/handle/123456789/266304 | - |
dc.description.abstract | Substituted azafluorenones were synthesized from dihalogeno diaryl ketones under palladium catalysis by combining, in auto-tandem processes, Suzuki coupling and intramolecular arylation reactions. Different dihalogenated diaryl ketones, prepared by sequential deprotocupration-aroylation, were identified as suitable substrates to this purpose. Conditions were identified to allow successful syntheses of several 6-/7-arylated 4-azafluorenones, 1-substituted 4-azafluorenones, 2-phenyl-3-azafluorenone, and 4-phenyl-3-azafluorenone from 3-(bromobenzoyl)-2-chloropyridines, 3-benzoyl-4-bromo-2-chloropyridines, 4-benzoyl-2,5-dichloropyridine, and 4-benzoyl-2,3-dichloropyridine, respectively. Some of the synthesized compounds exhibit interesting biological properties. | ru |
dc.description.sponsorship | Institut Universitaire de France (IUF) | ru |
dc.language.iso | en | ru |
dc.publisher | Elsevier Ltd | ru |
dc.subject | ЭБ БГУ::ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Физика | ru |
dc.title | Substituted azafluorenones: Access from dihalogeno diaryl ketones by palladium-catalyzed auto-tandem processes and evaluation of their antibacterial, antifungal, antimalarial and antiproliferative activities | ru |
dc.type | article | ru |
dc.rights.license | CC BY 4.0 | ru |
dc.identifier.DOI | 10.1016/j.tet.2015.12.050 | - |
dc.identifier.scopus | 84954393112 | - |
Располагается в коллекциях: | Статьи сотрудников НИИ ФХП |
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