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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
- Selective vicarious nucleophilic amination of 3-nitropyridines. Jan M. Bakke, Harald Svensen, Raffaela Trevisan
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 376
- Fast and efficient direct formation of size-controlled nanostructures of coordination polymers based on copper(i)–iodine bearing functional pyridine terminal ligands. Javier Conesa-Egea, Khaled Hassanein, Marta Muñoz, Félix Zamora, Pilar Amo-Ochoa
, Dalton Trans.
, 2018
, 47
, 5607
- Chromogenic naked-eye detection of copper ion and fluoride. Ye Won Choi, Jae Jun Lee, Ga Rim You, Sun Young Lee, Cheal Kim
, RSC Adv.
, 2015
, 5
, 86463
- 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
- Novel charge transfer supramolecular assemblies with Keggin anions and 2-amino-5-nitropyridine. J. A. F. Gamelas, F. M. Santos, V. Felix, A. M. V. Cavaleiro, E. de Matos Gomes, M. Belsley, M. G. B. Drew
, Dalton Trans.
, 2006
, 1197
- Intermolecular interactions in molecular crystals: what’s in a name?. Alison J. Edwards, Campbell F. Mackenzie, Peter R. Spackman, Dylan Jayatilaka, Mark A. Spackman
, Faraday Discuss.
, 2017
, 203
, 93
- Substitution reactions of 5-nitropyridine-2-sulfonic acid. A new pathway to 2,5-disubstituted pyridines. Jan M. Bakke, Ingrid Sletvold
, Org. Biomol. Chem.
, 2003
, 1
, 2710
- Dehydrative amination of benzhydrols with electron-withdrawing group-substituted 2-aminopyridines utilizing Au(iii)/TPPMS catalyst system in water. Hidemasa Hikawa, Taku Nakayama, Shunki Nakamura, Shoko Kikkawa, Isao Azumaya
, Org. Biomol. Chem.
, 2022
, 20
, 4183