Condensed bridgehead nitrogen heterocyclic systems: synthesis and bioactivity of s-triazolo [3,4-b] [1,3,4] thiadiazoles, s-triazolo [3,4-b] [1,3,4] thiadiazines and s-triazolo [3',4': 2,3]-thiadiazino [5,6-b]
quinoxaline. Indian Journal of Heterocyclic Chemistry, 10: 1-4.
A standard curve was prepared with the
quinoxaline of MGO (Sigma, Steinheim, Germany) in the range between 0.4 [micro]g/mL and 20 [micro]g/mL.
Johnson, "Synthesis, characterization, electrochemical and biological studies on some metal(II) Schiff base complexes containing
quinoxaline moiety," Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, vol.
Chitra, "Adsorption and density functional theory on corrosion of mild steel by a
quinoxaline derivative," Der Pharma Chemica, vol.
Hao et al., "In vitro antimicrobial activities of animal-used
quinoxaline 1,4-di-N-oxides against mycobacteria, mycoplasma and fungi," BMC Veterinary Research, vol.
It was reported that the reaction of 1,2-diaminoaromatic compound 1 with 1,2-dicarbonyl compounds 2 or 3 afforded the
quinoxaline or pyrazin-2(1H)-one derivatives 4 and 5 [1, 2].
Caption: Figure 16: Phthalazine, quinazoline, and
quinoxaline analogues of thiazolidinedione.
Zou, "Development of
quinoxaline based polymers for photovoltaic applications," Journal of Materials Chemistry C, vol.
Quinoxaline derivatives are known to have wide range of biological properties from antimicrobial effects to anticancer effects [27].