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For: Zheng H, Wang K, Zhang W, Liu R. Selenium Dioxide–Mediated Synthesis of Fused 1,2,4-Triazoles as Cytotoxic Agents. Synthetic Communications 2015;45:2849-56. [DOI: 10.1080/00397911.2015.1111384] [Cited by in Crossref: 13] [Cited by in F6Publishing: 5] [Article Influence: 1.9] [Reference Citation Analysis]
Number Citing Articles
1 Zribi L, Zribi F, Marco-contelles J, Chabchoub F, Ismaili L. Facile one-pot synthesis of new [1,2,4]triazolo[1,5- a ]pyridine derivatives by ultrasonic irradiation. Synthetic Communications 2017;47:1934-9. [DOI: 10.1080/00397911.2017.1357078] [Cited by in Crossref: 9] [Cited by in F6Publishing: 1] [Article Influence: 1.8] [Reference Citation Analysis]
2 Shao L, Li Y, Lu J, Jiang X. Recent progress in selenium-catalyzed organic reactions. Org Chem Front 2019;6:2999-3041. [DOI: 10.1039/c9qo00620f] [Cited by in Crossref: 57] [Article Influence: 19.0] [Reference Citation Analysis]
3 Kulikov AS, Epishina MA, Fershtat LL, Romanova AA, Makhova NN. Effective synthesis of 6-substituted 7H-tetrazolo[5,1-b][1,3,4]thiadiazines via a one-pot condensation/nitrosation/azide-tetrazole tautomerism reaction sequence. Tetrahedron Letters 2017;58:3998-4002. [DOI: 10.1016/j.tetlet.2017.09.014] [Cited by in Crossref: 12] [Cited by in F6Publishing: 4] [Article Influence: 2.4] [Reference Citation Analysis]
4 Ye Z, Ding M, Wu Y, Li Y, Hua W, Zhang F. Electrochemical synthesis of 1,2,4-triazole-fused heterocycles. Green Chem 2018;20:1732-7. [DOI: 10.1039/c7gc03739b] [Cited by in Crossref: 51] [Article Influence: 12.8] [Reference Citation Analysis]
5 Li E, Hu Z, Song L, Yu W, Chang J. Synthesis of 1,2,4-Triazolo[4,3- a ]pyridines and Related Heterocycles by Sequential Condensation and Iodine-Mediated Oxidative Cyclization. Chem Eur J 2016;22:11022-7. [DOI: 10.1002/chem.201601744] [Cited by in Crossref: 23] [Cited by in F6Publishing: 14] [Article Influence: 3.8] [Reference Citation Analysis]
6 Sachdeva T, Low ML, Mai C, Cheong SL, Liew YK, Milton MD. Design, Synthesis and Characterisation of Novel Phenothiazine‐Based Triazolopyridine Derivatives: Evaluation of Anti‐Breast Cancer Activity on Human Breast Carcinoma. ChemistrySelect 2019;4:12701-7. [DOI: 10.1002/slct.201903203] [Cited by in Crossref: 3] [Article Influence: 1.0] [Reference Citation Analysis]
7 Wen X, Zhou Y, Zeng J, Liu X. Recent Development of 1,2,4-triazole-containing Compounds as Anticancer Agents. CTMC 2020;20:1441-60. [DOI: 10.2174/1568026620666200128143230] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
8 Reddy LM, Reddy VV, Prathima PS, Reddy CK, Reddy BVS. Metal-free One-pot Synthesis of 1,2,4-Triazolo[4,3- a ]pyridines from 2-Hydrazinylpyridines. Adv Synth Catal 2018;360:3069-73. [DOI: 10.1002/adsc.201800512] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
9 El-sayed HA, Said SA, Abd El-hamid AM. An efficient and metal-free synthetic protocol for mono-, bis-, and spiro[1,2,4]triazolo[1,5- a ]pyridines utilizing 1,2-diaminopyridine derivative via C–N bond formation. Synthetic Communications 2021;51:3116-24. [DOI: 10.1080/00397911.2021.1961276] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Abdelli A, Azzouni S, Plais R, Gaucher A, Efrit ML, Prim D. Recent advances in the chemistry of 1,2,4-triazoles: Synthesis, reactivity and biological activities. Tetrahedron Letters 2021;86:153518. [DOI: 10.1016/j.tetlet.2021.153518] [Reference Citation Analysis]