A synthesis of functionalized 3-amino-1,2,4-triazoles from nitrile imines and guanidine derivatives
Author:
Publisher
Springer Science and Business Media LLC
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Molecular Biology,General Medicine,Information Systems,Catalysis
Link
https://link.springer.com/content/pdf/10.1007/s11030-022-10471-z.pdf
Reference21 articles.
1. Maddila S, Pagadala R, Jonnalagadda SB (2013) 1,2,4-Triazoles: a review of synthetic approaches and the biological activity. Lett Org Chem 10:693–714. https://doi.org/10.2174/157017861010131126115448
2. Abdelli A, Azzouni S, Plais R, Gaucher A, Efrit ML, Prim D (2021) Recent advances in the chemistry of 1,2,4-triazoles: synthesis, reactivity and biological activities. Tetrahedron Lett 86:153518. https://doi.org/10.1016/j.tetlet.2021.153518
3. Wei Z, Zhang Q, Tang M, Zhang S, Zhang Q (2021) Diversity-oriented synthesis of 1,2,4-Triazols, 1,3,4-Thiadiazols, and 1,3,4-Selenadiazoles from N-Tosylhydrazones. Org Lett 23:4436–4440. https://doi.org/10.1021/acs.orglett.1c01379
4. Sedash YV, Gorobets NY, Chebanov VA, Konovalova IS, Shishkin OV, Desenko SM (2012) Dotting the i’s in three-component Biginelli-like condensations using 3-amino1,2,4-triazole as a 1,3-binucleophile. RSC Adv 2:6719–6728. https://doi.org/10.1039/C2RA20195J
5. Guo K, Shelat AA, Guy RK, Kastan MB (2014) Development of a cell-based, high-throughput screening assay for ATM kinase inhibitors. J Biomol Screen 19:538–544. https://doi.org/10.1177/1087057113520325
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