Results 211 to 220 of about 29,559 (250)
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Synthetic Communications, 2019
In this report, we have described a convenient and eco-compatible approach for synthesis of new hybrid spiro[indeno[1,2-b]quinoxaline-[11,2′]-thiazolidine]-4′-ones (4a-k) via multi-component reaction of indeno[1,2-b]quinoxalinone, α-mercaptocarboxylic ...
Ruby Singh +3 more
semanticscholar +1 more source
In this report, we have described a convenient and eco-compatible approach for synthesis of new hybrid spiro[indeno[1,2-b]quinoxaline-[11,2′]-thiazolidine]-4′-ones (4a-k) via multi-component reaction of indeno[1,2-b]quinoxalinone, α-mercaptocarboxylic ...
Ruby Singh +3 more
semanticscholar +1 more source
Chemistry, 2019
Quinoxaline (Q), pyrido[2,3-b]pyrazine (PP) and pyrido[3,4-b]pyrazine (iPP) are used as electron acceptors (A) to design a series of D-π-A type light-emitting materials with different donor (D) groups.
Tingting Huang +3 more
semanticscholar +1 more source
Quinoxaline (Q), pyrido[2,3-b]pyrazine (PP) and pyrido[3,4-b]pyrazine (iPP) are used as electron acceptors (A) to design a series of D-π-A type light-emitting materials with different donor (D) groups.
Tingting Huang +3 more
semanticscholar +1 more source
The Chemistry and Applications of the Quinoxaline Compounds
Current organic chemistry, 2019The quinoxaline derivatives are beneficial compounds because of their various medicinal and industrial applications. They are well-known for application in organic light emitting devices, polymers and pharmaceutical agents.
M. Soleymani, M. Chegeni
semanticscholar +1 more source
ACS Applied Polymer Materials, 2019
We demonstrate, by screening a library of four derivatives of benzodithiophene–quinoxaline (BDT-QX)-based polymer, that BDT-QX are donor polymer candidates for large-scale coating of organic photov...
Audrey Laventure +6 more
semanticscholar +1 more source
We demonstrate, by screening a library of four derivatives of benzodithiophene–quinoxaline (BDT-QX)-based polymer, that BDT-QX are donor polymer candidates for large-scale coating of organic photov...
Audrey Laventure +6 more
semanticscholar +1 more source
Journal of Polymer Science Part A-1: Polymer Chemistry, 1972
AbstractA series of new amide–quinoxaline ordered copolymers derived from phthaloyl, isophthaloyl, and terephthaloyl chlorides have been synthesized and characterized. The isophthaloyl and terephthaloyl polymers had decomposition temperatures between 445–495°C and were soluble in a variety of solvents. These high molecular weight polymers were prepared
James V. Duffy, Joseph M. Augl
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AbstractA series of new amide–quinoxaline ordered copolymers derived from phthaloyl, isophthaloyl, and terephthaloyl chlorides have been synthesized and characterized. The isophthaloyl and terephthaloyl polymers had decomposition temperatures between 445–495°C and were soluble in a variety of solvents. These high molecular weight polymers were prepared
James V. Duffy, Joseph M. Augl
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Quinoxaline-1,4-dioxide derivatives inhibitory action in melanoma and brain tumor cells.
Future Medicinal Chemistry, 2019Aim: Quinoxaline-1,4-dioxide derivatives are synthetic heterocyclic compounds with multiple biological and pharmacological effects. In this study, we investigated the bioactivity of five quinoxaline-1,4-di-N-oxides derivatives in different animal cell ...
Liliana Silva +4 more
semanticscholar +1 more source
Tetrahedron, 1964
Abstract Base catalysed intramolecular cyclization of α-cyano- o -nitroacetanilides (Ia–d) to the corresponding 2-cyano-3-hydroxyquinoxaline 1-oxides (IIa-d) is described, and a mechanism proposed. The cyanoquinoxaline N-oxides (IIa-d) on reduction are deoxygenated with simultaneous loss of the nitrile group, and when heated with concentrated aqueous
Yusuf Ahmad, M.S. Habib, null Ziauddin
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Abstract Base catalysed intramolecular cyclization of α-cyano- o -nitroacetanilides (Ia–d) to the corresponding 2-cyano-3-hydroxyquinoxaline 1-oxides (IIa-d) is described, and a mechanism proposed. The cyanoquinoxaline N-oxides (IIa-d) on reduction are deoxygenated with simultaneous loss of the nitrile group, and when heated with concentrated aqueous
Yusuf Ahmad, M.S. Habib, null Ziauddin
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Quinoxaline/phenylquinoxaline copolymers
Journal of Applied Polymer Science, 1977AbstractThe thermal crosslinkability of the quinoxaline moiety incorporated within poly(phenylquinoxalines) was demonstrated by differential scanning calorimetry (DSC), torsional braid analysis (TBA), and high‐temperature adhesive evaluation. Several homopolymers, random copolymers, and polymer blends were prepared and evaluated.
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Crosslinked polyamide‐quinoxalines
Journal of Polymer Science: Polymer Letters Edition, 1973O, S, SO OR SO2 AND Y IS O-PHENYLENE, M-PHENYLENE, P-PHENYLENE OR- 1,2-DI(NH2-),4-((3,4-DI(NH2-)PHENYL)-X-)BENZENE WITH AN AMIDE OF THE FORMULA 1,3-BIS(PHENYL-CO-CO-Y-NH-CO-),5-(R-OOC-)BENZENE THESE POLYMERS FIND USE AS FILM OR COATINGS AND CAN ALSO BE MADE INTO FIBERS.
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