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- Synthesis and cytotoxicity evaluation of novel pyrido[3,4-d]pyrimidine derivatives as potential anticancer agents. Linyi Wei, Sanjay V. Malhotra
, Med. Chem. Commun.
, 2012
, 3
, 1250
- The electric dipole moments of chloro-anilines and of some chloro-, bromo-, and nitro-substituted amino-pyridines in benzene and 1,4-dioxan solutions. C. W. N. Cumper, A. Singleton
, J. Chem. Soc. B
, 1968
, 645
- Direct synthesis of novel quinoxaline derivatives via palladium-catalyzed reductive annulation of catechols and nitroarylamines. Feng Xie, Yibiao Li, Xiuwen Chen, Lu Chen, Zhongzhi Zhu, Bin Li, Yubing Huang, Kun Zhang, Min Zhang
, Chem. Commun.
, 2020
, 56
, 5997
- A palladium nanoparticle-catalyzed aryl–amine coupling reaction: high performance of aryl and pyridyl chlorides as the coupling partner. Debkumar Nandi, Rafique Ul Islam, Nishu Devi, Samarjeet Siwal, Kaushik Mallick
, New J. Chem.
, 2018
, 42
, 812
- A structural study of 2-amino-5-nitropyridine and 2-amino-3-nitropyridine: intermolecular forces and polymorphism. Christer B. Aakeröy, Alicia M. Beatty, Mark Nieuwenhuyzen, Min Zou
, J. Mater. Chem.
, 1998
, 8
, 1385
- Selective vicarious nucleophilic amination of 3-nitropyridines. Jan M. Bakke, Harald Svensen, Raffaela Trevisan
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 376
- Strong enhancement of second harmonic generation in nonlinear optical crystals: 2-amino-3-nitropyridinium halides (Cl, Br, I). Tianliang Chen, Zhihua Sun, Xitao Liu, Jinyun Wang, Yuelan Zhou, Chengmin Ji, Shuquan Zhang, Lina Li, Zhong-Ning Chen, Junhua Luo
, J. Mater. Chem. C
, 2014
, 2
, 8723
- Photophysical properties of structural isomers of homoleptic Ir-complexes derived from xylenyl-substituted N-heterocyclic carbene ligands. Bo-Sun Yun, Jin-Hyoung Kim, So-Yoen Kim, Ho-Jin Son, Dae Won Cho, Sang Ook Kang
, Phys. Chem. Chem. Phys.
, 2019
, 21
, 7155
- Chemical modulation of Kv7 potassium channels. Matteo Borgini, Pravat Mondal, Ruiting Liu, Peter Wipf
, RSC Med. Chem.
, 2021
, 12
, 483
- 379. Some reactions of substituted 2-bromopyridines. A. H. Berrie, G. T. Newbold, F. S. Spring
, J. Chem. Soc.
, 1952
, 2042