Selection of Conditions for Alkylation of 3-Amino-1,2,4-triazole

Sheldon, R.A., Bekkum, H.V., Fine Chemicals through Heterogeneous Catalysis, New York: John Wiley & Sons., 2008, p. 636.

Elangovan, S., Neumann, J., Sortais, J.-B., Junge, K., Darcel, C., Beller, M., Nat. Commun., 2016, vol. 7, no. 1, p. 1. https://doi.org/10.1038/ncomms12641

Article  CAS  Google Scholar 

Simplício, A.L., Clancy, J.M., Gilmer, J.F., Molecules, 2008, vol. 13, p. 519. https://doi.org/10.3390/molecules13030519

Article  PubMed  PubMed Central  Google Scholar 

Mashkovskii, M.D., Lekarstvennye sredstva (Medicines), Moscow: Novaya Volna, 2002.

Suvorova, Yu.V., Petukhova, E.A., Dmitriev, M.V., Danilova, E.A., Aleksandriiskii, V.V., ChemChemTech., 2021, vol. 4, no. 12, p. 8. https://doi.org/10.6060/ivkkt.20216412.6506

Article  CAS  Google Scholar 

Suvorova, Y.V., Petukhova, E.A., Dmitriev, M.V., Danilova, E.A., Russ. J. Gen. Chem., 2024, vol. 94, p. 297. https://doi.org/10.1134/S1070363224020051

Article  CAS  Google Scholar 

Hasratyan, A.H., Aleksanyan, A.G., Attaryan, H.S., Danagulyan, G.G., ChemChemTech., 2022, vol. 65, no. 1, p. 6. https://doi.org/10.6060/ivkkt.20226501.6485

Article  CAS  Google Scholar 

Bhattacharyya, S., Pathak, U., Mathur, S., Vishnoi, S., Jain, R., RSC Adv., 2014, vol. 4, p. 18229. https://doi.org/10.1039/C4RA01915F

Article  CAS  Google Scholar 

Llabres-Campaner, P.J., Ballesteros-Garrido, R., Ballesteros, R., Abarca, B., Tetrahedron, 2017, vol. 73, no. 37, p. 5552. https://doi.org/10.1016/j.tet.2017.08.006

Article  CAS  Google Scholar 

Chen, J., Peng, Z., Lu, M., Xiong, X., Chen, Z., Li, Q., Cheng, Z., Jiang, D., Tao, L., Hua, G., Bioorg. Med. Chem. Lett., 2018, vol. 28, p. 222. https://doi.org/10.1016/j.bmcl.2017.07.001

Article  PubMed  CAS  Google Scholar 

Danilova, E.A., Ivolin, A.A., Vorotsova, A.A., Islyaikin, M.K., Anan’eva, G.A., Zharnikova, N.V., Bykova, V.V., Usol’tseva, N.V., Zhidk. Krist. Praktich. Ispolz., 2011, no. 3, no. 37, p. 5.

Google Scholar 

Attarian, O.S., Matsoyan, S.G., Martirosyan, S.S., Chem. Heterocycl. Compd., 2005, vol. 41, p. 452. https://doi.org/10.1007/s10593-005-0170-z

Article  CAS  Google Scholar 

Boechat, N., Pinheiro Luiz, C.S., Osvaldo, A., Silva, I.C., Molecules, 2011, vol. 16, p. 8083. https://doi.org/10.3390/molecules16098083

Article  PubMed  PubMed Central  CAS  Google Scholar 

Sheldrick, G.M., Acta Crystallogr. (A), 2015, vol. 71, p. 3. https://doi.org/10.1107/S2053273314026370

Article  CAS  Google Scholar 

Sheldrick, G.M., Acta Crystallogr. (C), 2015, vol. 71, p. 3. https://doi.org/10.1107/S2053229614024218

Article  CAS  Google Scholar 

CrysAlisPro, Rigaku Oxford Diffraction, 2022, Version 1.171.42.74a.

Macrae, C.F., Bruno, I.J., Chisholm, J.A., Edgington, P.R., J. Appl. Cryst., 2008, vol. 41, p. 466. https://doi.org/10.1107/S0021889807067908

Article  CAS  Google Scholar 

Westrip, S.P., J. Appl. Cryst., 2010, vol. 43, p. 920. https://doi.org/10.1107/S0021889810022120

Article  CAS  Google Scholar 

Dolomanov, O.V., Bourhis, L.J., Gildea, R.J., Howard, J.A.K., Puschmann, H., J. Appl. Cryst., 2009, vol. 42, p. 339. https://doi.org/10.1107/S0021889808042726

Article  CAS  Google Scholar 

Filimonov, D.A., Druzhilovsky, D.S., Lagunin, A.A., Gloriozova, T.A., Rudik, A.V., Dmitriev, A.V., Pogodin, P.V., Poroikov, V.V., Biomed. Chem. Res. Method., 2018, vol. 1, no. 1, p. 1. https://doi.org/10.18097/BMCRM00004

Article  Google Scholar 

Poroikov V.V, Filimonov, D.A., Gloriozova, T.A., Lagunin, A.A., Druzhilovskii, D.S., Stepanchikova, A.V., Vestn. VOGiS., 2009, vol. 1, no. 13, p. 137.

Granovsky, A.A. Firefly Version, 8.1.0.

Andrienko, G.A. ChemCraft Version 1.8, build 428.

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