Results
1 -
10 of
46
(Click
here to explore results)
- Gas-phase pyrolysis of 4-amino-3-allylthio-1,2,4-triazoles: a new route to [1,3]thiazolo[3,2-b][1,2,4]triazoles. Dale D. J. Cartwright, Bernard A. J. Clark, Hamish McNab
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 424
- Stabilization of the Pd–NHC framework with 1,2,4-triazol-5-ylidene ligands toward decomposition in alkaline media. Andrey Yu. Chernenko, Alexander V. Astakhov, Vadim V. Kutyrev, Evgeniy G. Gordeev, Julia V. Burykina, Mikhail E. Minyaev, Victor N. Khrustalev, Victor M. Chernyshev, Valentine P. Ananikov
, Inorg. Chem. Front.
, 2021
, 8
, 3382
- Studies on the synthesis and properties of nitramino compounds based on tetrazine backbones. Shiyu Zhang, Guangbin Cheng, Hongwei Yang
, Dalton Trans.
, 2020
, 49
, 5590
- Synthetic studies on 4,5-dihydro-3H-1,2,4-triazole-3,5-diones bearing fluorogenic residues at N-4. Gordon Read, Nigel R. Richardson
, J. Chem. Soc., Perkin Trans. 1
, 1996
, 167
- Reactive intermediates. Part XXVI. Flash vacuum pyrolysis of phenyl-substituted 1,2,4-triazoles; a new synthesis of isoindoles. Thomas L. Gilchrist, Charles W. Rees, Colin Thomas
, J. Chem. Soc., Perkin Trans. 1
, 1975
, 12
- Diastereoselective synthesis of functionalised carbazoles via a sequential Diels–Alder/ene reaction strategy. Joseph Cowell, Matokah Abualnaja, Stephanie Morton, Ruth Linder, Faye Buckingham, Paul G. Waddell, Michael R. Probert, Michael J. Hall
, RSC Adv.
, 2015
, 5
, 16125
- Electrochemical synthesis of diverse sulfonamide derivatives depending on the potential electrode and their antimicrobial activity evaluation. F. Varmaghani, M. Hassan, D. Nematollahi, S. Mallakpour
, New J. Chem.
, 2017
, 41
, 8279
- Combining 1,2,4-triazole and pyrazole frameworks for new insensitive energetic materials. Changhao Dai, Jieyi Chen, Jie Tang, Guangbin Cheng, Hongwei Yang
, New J. Chem.
, 2021
, 45
, 17960
- Synthesis and structural characterization of 3,5-dinitro-1,2,4-triazolates. R. Haiges, G. Bélanger-Chabot, S. M. Kaplan, K. O. Christe
, Dalton Trans.
, 2015
, 44
, 2978
- Nitroimino as an energetic group in designing energetic materials for practical use, a tautomerism from nitroamino. Yaxi Wang, Lu Hu, Siping Pang, Jean'ne M. Shreeve
, J. Mater. Chem. A
, 2023
, 11
, 13876