154255-40-0Relevant articles and documents
Design, synthesis of quinolinyl Schiff bases and azetidinones as enoyl ACP-reductase inhibitors
Joshi, Shrinivas D.,More, Uttam A.,Parkale, Deepak,Aminabhavi, Tejraj M.,Gadad, Andanappa K.,Nadagouda, Mallikarjuna N.,Jawarkar, Rahul
, p. 3892 - 3911 (2015)
New series of quinoline derivatives were synthesized from 2-chloroquinoline-3-carbaldehydes. In the reaction sequence, substituted acetanilides were cyclized to give 2-chloroquinoline-3-carbaldehydes 2a-d, which were transformed to 6a-d, which were then c
Synthesis and antimicrobial evaluation of novel oxa(thia)diazolylquinolines and oxa(thia)diazepino[7,6-b] quinolines
Khalil,El-Sayed,El-Shamy
, p. 489 - 492 (2007/10/02)
Three novel series of quinoline derivatives have been prepared by cyclization of the intermediate 3[(substituted)thiocarbamoyl-hydrazonomethyl]-2-chloroquinolines and 3-aroylhydrazonomethyl-2-chloroquinolines: 3-(3-Acetyl-5-(substituted)-2,3-dihydro-1,3,4-oxa(thia)diazol-2-yl)-2- chloroquinolines(4; 5), 3-(5-(substituted)-1,3,4-oxa(thia)diazol-2-yl)-2-chloroquinolines (6; 7), and 2-(substituted)-1,3,4-oxa(thia)diazepino[7,6-b]quinolines (8; 9). The antimicrobial activity of these compounds was studied.