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For: Gavlik KD, Lesogorova SG, Sukhorukova ES, Subbotina JO, Slepukhin PA, Benassi E, Belskaya NP. Synthesis of 2-Aryl-1,2,3-triazoles by Oxidative Cyclization of 2-(Arylazo)ethene-1,1-diamines: A One-Pot Approach. Eur J Org Chem 2016;2016:2700-10. [DOI: 10.1002/ejoc.201600256] [Cited by in Crossref: 13] [Cited by in F6Publishing: 5] [Article Influence: 2.2] [Reference Citation Analysis]
Number Citing Articles
1 Huang L, Liu M, Man S, Ma D, Feng D, Sun Z, Guan Q, Zuo D, Wu Y, Zhang W, Bao K. Design, synthesis and bio-evaluation of novel 2-aryl-4-(3,4,5-trimethoxy-benzoyl)-5-substituted-1,2,3-triazoles as the tubulin polymerization inhibitors. European Journal of Medicinal Chemistry 2020;186:111846. [DOI: 10.1016/j.ejmech.2019.111846] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
2 Eltyshev AK, Agafonova IA, Minin AS, Pozdina VA, Shevirin VA, Slepukhin PA, Benassi E, Belskaya NP. Photophysics, photochemistry and bioimaging application of 8-azapurine derivatives. Org Biomol Chem 2021;19:9880-96. [PMID: 34734607 DOI: 10.1039/d1ob01801a] [Reference Citation Analysis]
3 Eltyshev AK, Minin AS, Smoliuk LT, Benassi E, Belskaya NP. 2-Aryl-2,4-dihydro-5 H -[1,2,3]triazolo[4,5- d ]pyrimidin-5-ones as a New Platform for the Design and Synthesis of Biosensors and Chemosensors: 2-Aryl-2,4-dihydro-5 H -[1,2,3]triazolo[4,5- d ]pyrimidin-5-ones as a New Platform for the Design and Synthesis of Biosensors and Chemosensors. Eur J Org Chem 2020;2020:316-29. [DOI: 10.1002/ejoc.201901582] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
4 Eltyshev AK, Suntsova PO, Karmatskaia KD, Taniya OS, Slepukhin PA, Benassi E, Belskaya NP. An effective and facile synthesis of new blue fluorophores on the basis of an 8-azapurine core. Org Biomol Chem 2018;16:9420-9. [PMID: 30500034 DOI: 10.1039/c8ob02644k] [Cited by in Crossref: 7] [Article Influence: 1.8] [Reference Citation Analysis]
5 Souza ROMA, Miranda LSME. Strategies Towards the Synthesis of N2-Substituted 1,2,3-Triazoles. An Acad Bras Cienc 2019;91:e20180751. [PMID: 30785471 DOI: 10.1590/0001-3765201820180751] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
6 Safronov NE, Fomin TO, Minin AS, Todorov L, Kostova I, Benassi E, Belskaya NP. 5-Amino-2-aryl-1,2,3-triazol-4-carboxylic acids: Synthesis, photophysical properties, and application prospects. Dyes and Pigments 2020;178:108343. [DOI: 10.1016/j.dyepig.2020.108343] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
7 Wu P, He Y, Wang H, Zhou Y, Yu Z. Copper(II)-Catalyzed C–H Nitrogenation/Annulation Cascade of Ketene N , S -Acetals with Aryldiazonium Salts: A Direct Access to N2 -Substituted Triazole and Triazine Derivatives. Org Lett 2020;22:310-5. [DOI: 10.1021/acs.orglett.9b04335] [Cited by in Crossref: 14] [Article Influence: 4.7] [Reference Citation Analysis]
8 Gavlik KD, Sukhorukova ES, Shafran YM, Slepukhin PA, Benassi E, Belskaya NP. 2-Aryl-5-amino-1,2,3-triazoles: New effective blue-emitting fluorophores. Dyes and Pigments 2017;136:229-42. [DOI: 10.1016/j.dyepig.2016.08.015] [Cited by in Crossref: 21] [Article Influence: 4.2] [Reference Citation Analysis]
9 Liu Z, Hao W, Gao W, Zhu G, Li X, Tong L, Tang B. Silver-catalyzed three-component reaction: synthesis of N2-substituted 1,2,3-triazoles via direct benzylic amination. Sci China Chem 2019;62:1001-6. [DOI: 10.1007/s11426-019-9455-0] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]