Features of the aminomethylation of 7-hydroxy-4'-fluoroisoflavones with primary amines
Дата
2010
ORCID
DOI
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Назва журналу
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Назва тому
Видавець
Анотація
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.
Опис
Ключові слова
8-aminomethylisoflavones, 3-(4-fluorophenyl)-9, 10-dihydro-4H, 8H-chromeno[8,7-e][1,3]oxa- zin-4-ones, aminomethylation, electrophilic substitution, ізофлавон, електрофільне заміщення, амінометилювання, 3,4-дигидро-1,3-бензоксазин, изофлавон, электрофильное замещение, аминометилирование, кафедра харчової хімії
Бібліографічний опис
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.