Please use this identifier to cite or link to this item: http://dspace.nuft.edu.ua/jspui/handle/123456789/3723
Title: Features of the aminomethylation of 7-hydroxy-4'-fluoroisoflavones with primary amines
Authors: Bondarenko, Svetlana
Frasinyuk, Mihaylo
Khilya, Volodimir
Бондаренко, Світлана Петрівна
Фрасинюк, Михайло Сергійович
Хиля, Володимир Петрович
Keywords: 8-aminomethylisoflavones
3-(4-fluorophenyl)-9
10-dihydro-4H
8H-chromeno[8,7-e][1,3]oxa- zin-4-ones
aminomethylation
electrophilic substitution
3,4-дигідро-1,3-бензоксазин
ізофлавон
електрофільне заміщення
амінометилювання
3,4-дигидро-1,3-бензоксазин
изофлавон
электрофильное замещение
аминометилирование
кафедра харчової хімії
Issue Date: 2010
Citation: Khilya, V. Features of the aminomethylation of 7-hydroxy-4'-fluoroisoflavones with primary amines / V. Khilya, M. Frasinyuk, S. Bondarenko // Chemistry of heterocyclic compounds. - 2010. - Т.46, № 2. - P. 146.
Abstract: The behavior of 7-hydroxy-4'-fluoroisoflavones under the conditions of the Mannich reaction with primary amines was studied. New 9-alkyl-substituted 3-(4-fluorophenyl)-9,10-dihydro-4H,8H-chromeno-[8,7-e][1,3]oxazin-4-ones were synthesized. A method was developed for the synthesis of 8-amino- methyl derivatives of isoflavones.
URI: http://dspace.nuft.edu.ua/jspui/handle/123456789/3723
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