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- Recent developments in the synthesis and biological activity of acridine/acridone analogues. Monika Gensicka-Kowalewska, Grzegorz Cholewiński, Krystyna Dzierzbicka
, RSC Adv.
, 2017
, 7
, 15776
- Boron trifluoride etherate promoted microwave-assisted synthesis of antimalarial acridones. Papireddy Kancharla, Rozalia A. Dodean, Yuexin Li, Jane X. Kelly
, RSC Adv.
, 2019
, 9
, 42284
- Ligand-regulated photoinduced electron transfer within metal–organic frameworks for efficient photocatalysis. Yang Tang, Guanfeng Ji, Hanning Li, Hui Gao, Cheng He, Liang Zhao, Chunying Duan
, Inorg. Chem. Front.
, 2023
, 10
, 5439
- Acridin-9(10H)-one based thermally activated delayed fluorescence material: simultaneous optimization of RISC and radiation processes to boost luminescence efficiency. Yongqiang Mei, Di Liu, Jiuyan Li, Huiting Li, Wenkui Wei
, J. Mater. Chem. C
, 2021
, 9
, 5885
- Synthesis and evaluation of the antitumor activity of polyhalo acridone derivatives. Chao Huang, Sheng-Jiao Yan, Xiang-Hui Zeng, Bo Sun, Min-Bo Lan, Jun Lin
, RSC Adv.
, 2015
, 5
, 17444
- A bisubstrate reagent orchestrating adenosine triphosphate and l-tyrosine and making tyrosyl adenylate: partial mimicking of tyrosyl-tRNA synthetase. Harpreet Singh, Baljit Kaur, Harpreet Kaur, Palwinder Singh
, Org. Biomol. Chem.
, 2018
, 16
, 9446
- Synthesis, characterization and biological evaluation of carboranylmethylbenzo[b]acridones as novel agents for boron neutron capture therapy. A. Filipa F. da Silva, Raquel S. G. R. Seixas, Artur M. S. Silva, Joana Coimbra, Ana C. Fernandes, Joana P. Santos, António Matos, José Rino, Isabel Santos, Fernanda Marques
, Org. Biomol. Chem.
, 2014
, 12
, 5201
- Strategically designed biomodel: engineering C3–C4 cleavage of d-fructose. Palwinder Singh, Arun Kumar, Sukhmeet Kaur, Amrinder Singh
, Org. Biomol. Chem.
, 2015
, 13
, 4210
- Unusual preservation of polyhedral molecular building units in a metal–organic framework with evident desymmetrization in ligand design. Yabo Xie, Hui Yang, Zhiyong U. Wang, Yangyang Liu, Hong-Cai Zhou, Jian-Rong Li
, Chem. Commun.
, 2014
, 50
, 563
- Accelerating PLQY and RISC rates in deep-blue TADF materials with the acridin-9(10H)-one acceptor by tuning the peripheral groups on carbazole donors. Yongqiang Mei, Di Liu, Jiuyan Li, Jiahui Wang
, J. Mater. Chem. C
, 2022
, 10
, 16524