Quinoxalinone as a privileged platform in drug development

L Shi, W Hu, J Wu, H Zhou, H Zhou… - Mini Reviews in …, 2018 - ingentaconnect.com
Among the family of nitrogen-containing heterocycles, quinoxalinone (or quinoxalin-2-one)
core, characterized by pyrazin-2 (1H)-one fused to benzene ring at two adjacent carbon …

BODIPY-based donor–acceptor π-conjugated alternating copolymers

BC Popere, AM Della Pelle, S Thayumanavan - Macromolecules, 2011 - ACS Publications
Four novel π-conjugated copolymers incorporating 4, 4-difluoro-4-borata-3a-azonia-4a-aza-
s-indacene (BODIPY) core as the “donor” and quinoxaline (Qx), 2, 1, 3-benzothiadiazole …

Wide bandgap copolymers based on quinoxalino [6, 5‐f]. quinoxaline for highly efficient nonfullerene polymer solar cells

T Yu, X Xu, G Zhang, J Wan, Y Li… - advanced functional …, 2017 - Wiley Online Library
Two novel wide bandgap copolymers based on quinoxalino [6, 5‐f] quinoxaline (NQx)
acceptor block, PBDT–NQx and PBDTS–NQx, are successfully synthesized for efficient …

N-Fused quinoxalines and benzoquinoxalines as attractive emitters for organic light emitting diodes

BD Lindner, Y Zhang, S Höfle, N Berger… - Journal of Materials …, 2013 - pubs.rsc.org
We describe the modular synthesis of quinoxaline fluorophores exhibiting strong
fluorescence over the whole visible spectrum. Based on their fluorescence quantum yield …

An efficient synthesis of quinoxalinone derivatives as potent inhibitors of aldose reductase

Y Yang, S Zhang, B Wu, M Ma, X Chen, X Qin… - …, 2012 - Wiley Online Library
A novel and facile synthesis of quinoxalinone derivatives was developed in which a wide
range of 3‐chloroquinoxalin‐2 (1H)‐ones as key intermediates can be generated chemo …

Thiadiazoloquinoxaline–Acetylene Containing Polymers as Semiconductors in Ambipolar Field Effect Transistors

T Dallos, D Beckmann, G Brunklaus… - Journal of the …, 2011 - ACS Publications
Two conjugated copolymers, PPTQT and PTTQT, were developed based on
thiadiazoloquinoxalines connected via ethynylene π-spacer to thiophene units. PPTQT …

Highly systematic and efficient HOMO–LUMO energy gap control of thiophene-pyrazine-acenes

LV Brownell, KA Robins, Y Jeong, Y Lee… - The Journal of …, 2013 - ACS Publications
We report a series of unique and simple donor–acceptor–donor molecular systems that
provide compelling insights into the highest occupied molecular orbital–lowest unoccupied …

Synthesis and Characterization of [1, 2, 5] Chalcogenazolo [3, 4-f] benzo [1, 2, 3] triazole and [1, 2, 3] Triazolo [3, 4-g] quinoxaline Derivatives

TL Tam, H Li, YM Lam, SG Mhaisalkar… - Organic …, 2011 - ACS Publications
The synthesis and characterization is reported of low bandgap [1, 2, 5] chalcogenazolo [3, 4-
f] benzo [1, 2, 3] triazole and [1, 2, 3] triazolo [3, 4-g] quinoxaline derivatives that display …

Highly Emissive Far Red/Near‐IR Fluorophores Based on Borylated Fluorene–Benzothiadiazole Donor–Acceptor Materials

DL Crossley, I Vitorica‐Yrezabal… - … A European Journal, 2016 - Wiley Online Library
Abstract Stille, Suzuki–Miyaura and Negishi cross‐coupling reactions of bromine‐
functionalised borylated precursors enable the facile, high yielding, synthesis of borylated …

Benzodithiophene–Thiadiazoloquinoxaline as an acceptor for ambipolar copolymers with deep LUMO level and distinct linkage pattern

C An, SR Puniredd, X Guo, T Stelzig, Y Zhao… - …, 2014 - ACS Publications
Two new conjugated copolymers, PBDTTQ-1 and PBDTTQ-2, with a distinct linked pattern
between benzodithiophene–thiadiazoloquinoxaline (BDTTQ) as acceptor and bithiophene …