Selective synthesis of a novel glycoluril-based hybrid compound with high application potential

Selective synthesis of a novel glycoluril-based hybrid compound with high application potential

Highly selective synthesis of a new antipyrine-substituted tetracycle was implemented on the basis of a modified Mannich reaction as a result of the condensation of glycoluril with 4-aminoantipyrine in formalin without the use of catalysts.

Bibliographic Details
Published in:Chemistry of heterocyclic compounds Vol. 57, № 6. P. 700-703
Main Author: Mamaeva, Elena А.
Other Authors: Leppa, Anastasiya V., Bakibaev, Abdigali A.
Format: Article
Language:English
Subjects:
4-аминоантипирин
бициклические бисмочевины
гликолурил
аминометилирование
конденсация
Манниха реакция
статьи в журналах
Online Access:http://vital.lib.tsu.ru/vital/access/manager/Repository/koha:000897213
Перейти в каталог НБ ТГУ
Description
Summary:Highly selective synthesis of a new antipyrine-substituted tetracycle was implemented on the basis of a modified Mannich reaction as a result of the condensation of glycoluril with 4-aminoantipyrine in formalin without the use of catalysts.
Bibliography:Библиогр.: 45 назв.
ISSN:0009-3122

Similar Items