An alternative method to access diverse N,N′-diquaternised-3,3′-biquinoxalinium “biquinoxen” dications [PDF]
An alternative synthetic route for the design of N,N′-diquaternised-3,3′-biquinoxalinium “biquinoxen” dications is reported, involving oxidative radical coupling of dithionite reduced quinoxaline quaternary salts.
Leblanc, Nicolas +2 more
core +1 more source
Density Functional Theory (DFT) using the B3LYP functional and Quantitative Structure-Activity Relationship QSAR studies is reported on some quinoxaline derivatives namely 3-methyl-2-phenyl quinoxaline (MPQ), 2,3-diphenyl quinoxaline (PPQ), 3-methyl-2(2 ...
Mwadham M. Kabanda, Eno E. Ebenso
doaj +1 more source
DISCOVERY OF TRIKETONE-QUINOXALINE HYBRIDS AS POTENT HPPD INHIBITORS USING STRUCTURE-BASED DRUG DESIGN [PDF]
<List> <ListItem><ItemContent><p>• HPPD is one of the most promising targets for new herbicides.</p></ItemContent></ListItem> <ListItem><ItemContent><p>• A family of novel HPPD ...
Baifeng ZHENG, Yaochao YAN, Can FU, Guangyi HUANG, Long ZHAO, Qiong CHEN, Renyu QU, Guangfu YANG
doaj +1 more source
Microwave assisted synthesis of quinoxaline derivatives
Substituted quinoxalines are known building blocks for compounds with pharmacological, agricultural, and material uses. Forming carbon-heteroatom bonds at the 2,3-positions on quinoxaline can be challenging. 2,3-chloroquinoxaline can undergo nucleophilic aromatic substitution however it must be in the presence of metal catalysts.
Lucas K. Beagle +3 more
openaire +2 more sources
Quinoxalines, a class of N-heterocyclic compounds, are important biological agents, and a significant amount of research activity has been directed towards this class.
Hena Khatoon, Emilia Abdulmalek
doaj +1 more source
Sinteza, in vitro antitumorsko ispitivanje i radiosenzitirajuće vrednovanje novih derivata 4-[3-(supstituiranih)tioureido]-N-(kinoksalin-2-il)benzensulfonamida [PDF]
Sulfonamides and quinoxaline derivatives possess many types of biological activities and have been recently reported to show substantial antitumor activity. This paper reports the synthesis of novel thioureidosulfaquinoxaline derivatives.
A. Budakoti +19 more
core +2 more sources
Synthesis and biological evaluation of novel substituted pyrrolo[1,2-a]quinoxaline derivatives as inhibitors of the human protein kinase CK2 [PDF]
Herein we describe the synthesis and properties of substituted phenylaminopyrrolo[1,2-a]quinoxaline-carboxylic acid derivatives as a novel class of potent inhibitors of the human protein kinase CK2.
Alvarez, Lautaro Damian +13 more
core +4 more sources
Substitutions of fluorine atoms and phenoxy groups in the synthesis of quinoxaline 1,4-di-N-oxide derivatives. [PDF]
The unexpected substitution of fluorine atoms and phenoxy groups attached to quinoxaline or benzofuroxan rings is described. The synthesis of 2-benzyl- and 2-phenoxy- 3-methylquinoxaline 1,4-di-N-oxide derivatives was based on the classical Beirut ...
Aldana, I. (Ignacio) +7 more
core +2 more sources
We report the synthesis and antimalarial activities of eighteen quinoxaline and quinoxaline 1,4-di-N-oxide derivatives, eight of which are completely novel. Compounds 1a and 2a were the most active against Plasmodium falciparum strains.
Ana Gil +7 more
doaj +1 more source
1,4-Di-N-oxide quinoxaline-2-carboxamide: Cyclic voltammetry and relationship between electrochemical behavior, structure and anti-tuberculosis activity [PDF]
To gain insight into the mechanism of action, the redox properties of 37 quinoxaline-2-carboxamide 1,4-di-N-oxides with varying degrees of anti-tuberculosis activity were studied in dimethylformamide (DMF) using cyclic voltammetry and first derivative ...
Aldana, I. (Ignacio) +8 more
core +1 more source

