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- Sulfonamide-1,3,5-triazine–thiazoles: discovery of a novel class of antidiabetic agents via inhibition of DPP-4. Hai-De Gao, Peng Liu, Yang Yang, Fang Gao
, RSC Adv.
, 2016
, 6
, 83438
- An experimental and theoretical investigation of the molecular and electronic structure of 2-amino-4-chloro-6-pyrazolyl-[1,3,5]triazine, forming supramolecular linear tapes in the solid state. Maurizio Casarin, Federica Garau, Magda Monari, Luciano Pandolfo, Claudio Pettinari, Alfonso Venzo
, New J. Chem.
, 2008
, 32
, 358
- 876. The search for chemotherapeutic amidines. Part XVI. Amidinoanilino-1,3,5-triazines and related compounds. J. N. Ashley, S. S. Berg, R. D. MacDonald
, J. Chem. Soc.
, 1960
, 4525
- Supramolecular self-assembly of triazine-based small molecules: targeting the endoplasmic reticulum in cancer cells. Chandramouli Ghosh, Aditi Nandi, Sudipta Basu
, Nanoscale
, 2019
, 11
, 3326
- Synthesis of a series of dichloroamino- and dihalosulfonamido-1,3,5-triazines and investigation of their hindered rotation and stereodynamic behaviour by NMR spectroscopy. Stuart A. Brewer, Helen T. Burnell, Ian Holden, Brian G. Jones, Colin R. Willis
, J. Chem. Soc., Perkin Trans. 2
, 1999
, 1231
- Tandem deprotonation/azide–tetrazole tautomerization of 4,6-diazido-N-nitro-1,3,5-triazin-2-amine in dimethylsulfoxide solutions: a theoretical study. S. V. Chapyshev, E. N. Ushakov
, Phys. Chem. Chem. Phys.
, 2015
, 17
, 17296
- Self-assembly of hydrogen-bonded supramolecular strands from complementary melamine and barbiturate components with chiral selection. K. C. Russell, J.-M. Lehn, N. Kyritsakas, A. DeCian, J. Fischer
, New J. Chem.
, 1998
, 22
, 123
- Efficient light-driven hydrogen evolution and azo dye degradation over the GdVO4@g-C3N4 heterostructure. Fahad A. Alharthi, Adel El Marghany, Naaser A. Y. Abduh, Imran Hasan
, RSC Adv.
, 2023
, 13
, 20417
- Recent biological applications of heterocyclic hybrids containing s-triazine scaffold. Muhammad Imran Ali, Muhammad Moazzam Naseer
, RSC Adv.
, 2023
, 13
, 30462
- Novel trinitroethanol derivatives: high energetic 2-(2,2,2-trinitroethoxy)-1,3,5-triazines. Alexander A. Gidaspov, Vladimir A. Zalomlenkov, Vladimir V. Bakharev, Victor E. Parfenov, Evgeniy V. Yurtaev, Marina I. Struchkova, Nadezhda V. Palysaeva, Kyrill Yu Suponitsky, David B. Lempert, Aleksei B. Sheremetev
, RSC Adv.
, 2016
, 6
, 34921