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dc.contributor.authorОнисько, Михайло Юрійович-
dc.contributor.authorФілак, Ігор Олегович-
dc.contributor.authorЛендєл, Василь Георгійович-
dc.date.accessioned2017-10-29T12:05:07Z-
dc.date.available2017-10-29T12:05:07Z-
dc.date.issued2017-
dc.identifier.citationMikhajlo Onysko, Igor Filak and Vasyl Lendel. Halogenoheterocyclization of terminallysubstituted 2-allylthio(seleno)quinolin-3-carbaldehydes. Heterocycl. Commun. 2017; 23(4): 309–312uk
dc.identifier.urihttps://dspace.uzhnu.edu.ua/jspui/handle/lib/16495-
dc.description.abstractElectrophilic heterocyclization of 2-alkenyllthioquinolin-3-carbaldehydes or 2-alkenylselenoquinolin- 3-carbaldehydes 2, 3 under the action of iodine or bromine non-regioselectively leads to the formation of fused quinolinium trihalogenides 4, 5. Type of the chalcogen atom does not affect regiochemistry of halogenation. Keywords: 2-alkenylselanyl; 2-alkenylsulfanyl; electrophilic cyclization; haloheterocyclization; 3-quinolinecarbaldehyde.uk
dc.language.isoenuk
dc.titleHalogenoheterocyclization of terminally substituted 2-allylthio(seleno)quinolin- 3-carbaldehydesuk
dc.typeTextuk
dc.pubTypeСтаттяuk
Appears in Collections:Наукові публікації кафедри органічної хімії

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