Design and synthesis of some substituted thiazolo[3,2-a]pyrimidine derivatives of potential biological activities
In continuation to our previous work, thiazolopyrimidines 2a-x were synthesized through intramolecular cyclization of 2-phenacylthio-dihydropyrimidine hydrobromides 1a-x using polyphosphoric acid. On the other hand, thiazolo[3,2-a]pyrimidine-3-one 3 was coupled with aryldiazonium salts or condensed...
Сохранить в:
Главные авторы: | Samia G. Abdel Moty (Автор), Mostafa A. Hussein (Автор), Salah A. Abdel Aziz (Автор), Mahrous A. Abou-Salim (Автор) |
---|---|
Формат: | |
Опубликовано: |
Elsevier,
2016-03-01T00:00:00Z.
|
Предметы: | |
Online-ссылка: | Connect to this object online. |
Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|
Схожие документы
-
Design, synthesis, docking, and anticancer evaluations of new thiazolo[3,2-a] pyrimidines as topoisomerase II inhibitors
по: Mona S. El-Zoghbi, и др.
Опубликовано: (2023) -
Synthesis of some substituted pyrimidines via cycloaddition reaction of amidines and chalcones
по: H. M. Al-Ajely, и др.
Опубликовано: (2009) -
p-TSA-promoted syntheses of 5H-benzo[h]thiazolo[2,3-b]quinazoline and indeno[1,2-d]thiazolo[3,2-a]pyrimidine analogs: molecular modeling and in vitro antitumor activity against hepatocellular carcinoma
по: Keshari AK, и др.
Опубликовано: (2017) -
Novel Glu-based pyrazolo[3,4-d]pyrimidine analogues: design, synthesis and biological evaluation as DHFR and TS dual inhibitors
по: Mater Mahnashi, и др.
Опубликовано: (2023) -
Novel topoisomerase II/EGFR dual inhibitors: design, synthesis and docking studies of naphtho[2',3':4,5]thiazolo[3,2-a]pyrimidine hybrids as potential anticancer agents with apoptosis inducing activity
по: Mai A. E. Mourad, и др.
Опубликовано: (2023)