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- Synthesis and in vitro evaluation of naphthalimide–benzimidazole conjugates as potential antitumor agents. Iqubal Singh, Vijay Luxami, Kamaldeep Paul
, Org. Biomol. Chem.
, 2019
, 17
, 5349
- Synthesis and photophysical properties of novel fluorescent materials containing 2,4,6-triphenylpyridine and 1,8-naphthalimide units using Suzuki reaction. Hui-Yan Liu, Liang-Feng Chen, Hai-Ying Wang, Yu Wan, Hui Wu
, RSC Adv.
, 2016
, 6
, 94833
- Synthesis and in vitro anti-proliferative evaluation of naphthalimide–chalcone/pyrazoline conjugates as potential SERMs with computational validation. Shalini, Pankaj, Sourav Taru Saha, Mandeep Kaur, Ebenezer Oluwakemi, Paul Awolade, Parvesh Singh, Vipan Kumar
, RSC Adv.
, 2020
, 10
, 15836
- Synthesis and photobiological applications of naphthalimide–benzothiazole conjugates: cytotoxicity and topoisomerase IIα inhibition. Iqubal Singh, Vijay Luxami, Diptiman Choudhury, Kamaldeep Paul
, RSC Adv.
, 2022
, 12
, 483
- Fluorescent aryl naphthalene dicarboximides with large Stokes shifts and strong solvatochromism controlled by dynamics and molecular geometry. Robert Greiner, Thorben Schlücker, Dominik Zgela, Heinz Langhals
, J. Mater. Chem. C
, 2016
, 4
, 11244
- Enhanced ion binding by the benzocrown receptor and a carbonyl of the aminonaphthalimide fluorophore in water-soluble logic gates. Andreas Diacono, Marie Claire Aquilina, Andrej Calleja, Godfrey Agius, Gabriel Gauci, Konrad Szaciłowski, David C. Magri
, Org. Biomol. Chem.
, 2020
, 18
, 4773
- Novel 1,8-naphthalimide derivatives for standard-red organic light-emitting device applications. Shuai Luo, Jie Lin, Jie Zhou, Yi Wang, Xingyuan Liu, Yan Huang, Zhiyun Lu, Changwei Hu
, J. Mater. Chem. C
, 2015
, 3
, 5259
- Synthesis of 3,4-dihydroxy-1,8-naphthalimides with inbuilt catechol and crown ether functionalities. Elley E. Rudebeck, Trent D. Ashton, Adam F. Henwood, Thorfinnur Gunnlaugsson, Frederick M. Pfeffer
, Org. Biomol. Chem.
, 2023
, 21
, 5970
- 1,8-Naphthalimide-based nonfullerene acceptors for wide optical band gap polymer solar cells with an ultrathin active layer thickness of 35 nm. Jicheng Zhang, Hongmei Xiao, Xuejuan Zhang, Yang Wu, Guangwu Li, Cuihong Li, Xuebo Chen, Wei Ma, Zhishan Bo
, J. Mater. Chem. C
, 2016
, 4
, 5656
- Bis-naphthalimides bridged by electron acceptors: optical and self-assembly characteristics. Ankita Saini, K. R. Justin Thomas
, RSC Adv.
, 2016
, 6
, 71638