1373349-71-3Relevant academic research and scientific papers
Cell cycle arrest and induction of apoptosis of newly synthesized pyranoquinoline derivatives under microwave irradiation
Fouda, Ahmed M.,Youssef, Ayman M. S.,Afifi, Tarek H.,Mora, Ahmed,El-Agrody, Ahmed M.
, p. 668 - 680 (2019/03/23)
A set of 2-amino-4-aryl-4H-pyrano[3,2-h]quinoline-3-carbonitrile derivatives were prepared via a one-pot, three-component condensation reaction between the substituted hydroxyquinoline derivatives, some aryl and/or hetaryl aldehydes, and malononitrile in
Halogenated 2-amino-4H-pyrano[3,2-h]quinoline-3-carbonitriles as antitumor agents and structure–activity relationships of the 4-, 6-, and 9-positions
Fouda, Ahmed M.
, p. 302 - 313 (2017/01/28)
A series of halogenated 2-amino-4-aryl-4H-pyrano[3,2-h]quinoline-3-carbonitrile derivatives were prepared via interaction of 8-hydroxyquinoline, 5-chloro-8-hydroxyquinoline, and 8-hydroxy-2-methylquinoline with various α-cyanocinnamonitriles. The assignme
Synthesis, antitumor activity, and structure-activity relationship of some 4H-pyrano[3,2-h]quinoline and 7H-pyrimido[4′,5′:6,5]pyrano[3,2-h] quinoline derivatives
El-Agrody, Ahmed M.,Abd-Rabboh, Hisham S. M.,Al-Ghamdi, Abdullah M.
, p. 1339 - 1355 (2013/04/10)
Several 4H-pyrano[3,2-h]quinoline (3a-d, 4a, 7a,b, 9a-c, 10a,b, 11a,b, and 13a-c) and 7H-pyrimido[4′,5′:6,5]pyrano[3,2-h]quinoline derivatives (8a-c) were obtained by treatment of 8-hydroxyquinoline (1a) and 8-hydroxy-2-methylquinoline (1b) with α-cyano-p
Synthesis of certain novel 4H-pyrano[3,2-h]quinoline derivatives
El-Agrody, Ahmed M.,Al-Ghamdi, Abdullah M.
experimental part, p. 134 - 146 (2012/02/04)
Treatment of 8-hydroxyquinoline 1a and 8-hydroxy-2-methylquinoline 1b with α-cyano-pchloro/bromocinnamonitriles 2a,b provided 4H-pyrano[3,2-h] quinoline-3-carbonitrile derivatives 3a-d, while treatment of (E) 2-(4-chlorostyryl)-8-hydroxyquinoline 7 with α
