Please use this identifier to cite or link to this item: https://dspace.uzhnu.edu.ua/jspui/handle/lib/16495
Title: Halogenoheterocyclization of terminally substituted 2-allylthio(seleno)quinolin- 3-carbaldehydes
Authors: Онисько, Михайло Юрійович
Філак, Ігор Олегович
Лендєл, Василь Георгійович
Issue Date: 2017
Citation: Mikhajlo Onysko, Igor Filak and Vasyl Lendel. Halogenoheterocyclization of terminallysubstituted 2-allylthio(seleno)quinolin-3-carbaldehydes. Heterocycl. Commun. 2017; 23(4): 309–312
Abstract: Electrophilic 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.
Type: Text
Publication type: Стаття
URI: https://dspace.uzhnu.edu.ua/jspui/handle/lib/16495
Appears in Collections:Наукові публікації кафедри органічної хімії

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