Supporting Information
The Supporting Information contains detailed descriptions of the reactions and protocols as well as the characterization of all target compounds.
| Supporting Information File 1: Experimental section and characterization data, biological assay details, and data availability in chemotion repository. | ||
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| Supporting Information File 2: Copies of spectra. | ||
| Format: PDF | Size: 10.7 MB | Download |
| Supporting Information File 3: Direkt links to datasets and reference numbers of target compounds in Molecule Archive. | ||
| Format: XLSX | Size: 12.5 KB | Download |
Cite the Following Article
Synthesis of new pyrazolo[1,2,3]triazines by cyclative cleavage of pyrazolyltriazenes
Nicolai Wippert, Martin Nieger, Claudine Herlan, Nicole Jung and Stefan Bräse
Beilstein J. Org. Chem. 2021, 17, 2773–2780.
https://doi.org/10.3762/bjoc.17.187
How to Cite
Wippert, N.; Nieger, M.; Herlan, C.; Jung, N.; Bräse, S. Beilstein J. Org. Chem. 2021, 17, 2773–2780. doi:10.3762/bjoc.17.187
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Scholarly Works
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- Ahmad, M. I.; Veg, E.; Joshi, S.; Khan, A. R.; Khan, T. Thiosemicarbazone Derivatives in Search of Potent Medicinal Agents: QSAR Approach (A Review). Russian Journal of General Chemistry 2024, 94, 2470–2495. doi:10.1134/s1070363224090251
- Gräßle, S.; Holzhauer, L.; Wippert, N.; Fuhr, O.; Nieger, M.; Jung, N.; Bräse, S. Synthesis of substituted triazole-pyrazole hybrids using triazenylpyrazole precursors. Beilstein journal of organic chemistry 2024, 20, 1396–1404. doi:10.3762/bjoc.20.121
- Aitken, R. A.; Fotherby, F. M. Triazines, tetrazines, and fused ring polyaza systems. Progress in Heterocyclic Chemistry; Elsevier, 2023; pp 469–485. doi:10.1016/b978-0-443-18939-5.00019-6
