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For: 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]
Number Citing Articles
1 Chen W, Du Y, Wang M, Fang Y, Yu W, Chang J. Synthesis of benzo[4,5]imidazo[1,2- a ]quinoxalines by I 2 -mediated sp 3 C–H amination. Org Chem Front 2020;7:3705-8. [DOI: 10.1039/d0qo01101k] [Cited by in Crossref: 7] [Article Influence: 3.5] [Reference Citation Analysis]
2 Bisht GS, Dunchu TD, Gnanaprakasam B. Synthesis of Quaternary Spirooxindole 2H-Azirines under Batch and Continuous Flow Condition and Metal Assisted Umpolung Reactivity for the Ring-Opening Reaction. Chem Asian J 2021;16:656-65. [PMID: 33464707 DOI: 10.1002/asia.202001418] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Jiao S, Wang Z, Zhao Q, Yu W, Chang J. Synthesis of fused 3-amino-1,2,4-triazoles via sequential addition of aryl hydrazines to isothiocyanates and I 2 -mediated cyclodesulfurization. Tetrahedron 2018;74:3069-73. [DOI: 10.1016/j.tet.2018.05.009] [Cited by in Crossref: 9] [Article Influence: 2.3] [Reference Citation Analysis]
4 Teng H, Tian J, Sun D, Xiu M, Zhang Y, Qiang X, Tang H, Guo Y. A mitochondria-specific fluorescent probe based on triazolopyridine formation for visualizing endogenous hypochlorous acid in living cells and zebrafish. Sensors and Actuators B: Chemical 2020;319:128288. [DOI: 10.1016/j.snb.2020.128288] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 4.5] [Reference Citation Analysis]
5 Inturi SB, Kalita B, Ahamed AGJ. Highly Efficient Synthesis of 4,3-Fused 1,2,4-Triazoles via One-Pot Multicomponent Domino Reaction Catalyzed by KI/TBHP. ChemistrySelect 2017;2:8377-82. [DOI: 10.1002/slct.201701566] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
6 Wu CJ, Wu JQ, Hu Y, Pu S, Lin Y, Zeng Z, Hu J, Chen WH. Design, synthesis and biological evaluation of indole-based [1,2,4]triazolo[4,3-a] pyridine derivatives as novel microtubule polymerization inhibitors. Eur J Med Chem 2021;223:113629. [PMID: 34175541 DOI: 10.1016/j.ejmech.2021.113629] [Reference Citation Analysis]
7 Hu S, Yang Z, Chen Z, Wu X. Metal‐Free Synthesis of 5‐Trifluoromethyl‐1,2,4‐Triazoles from Iodine‐Mediated Annulation of Trifluoroacetimidoyl Chlorides and Hydrazones. Adv Synth Catal 2019;361:4949-54. [DOI: 10.1002/adsc.201900983] [Cited by in Crossref: 22] [Cited by in F6Publishing: 8] [Article Influence: 7.3] [Reference Citation Analysis]
8 Baeten M, Maes BU. Carbon–Nitrogen Bond Formation Through Cross-Dehydrogenative Coupling Reactions. Elsevier; 2017. pp. 401-81. [DOI: 10.1016/bs.adomc.2017.04.003] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 2.2] [Reference Citation Analysis]
9 Xu H, Chen K, Liu H, Wang G. Solvent-free N -iodosuccinimide-promoted synthesis of spiroimidazolines from alkenes and amidines under ball-milling conditions. Org Chem Front 2018;5:2864-9. [DOI: 10.1039/c8qo00723c] [Cited by in Crossref: 14] [Article Influence: 3.5] [Reference Citation Analysis]
10 Fang B, Hou J, Tian J, Yu W, Chang J. Synthesis of phenanthridines by I 2 -mediated sp 3 C–H amination. Org Biomol Chem 2020;18:3312-23. [DOI: 10.1039/d0ob00433b] [Cited by in Crossref: 9] [Cited by in F6Publishing: 1] [Article Influence: 4.5] [Reference Citation Analysis]
11 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]
12 Reddy Lonka M, Zhang J, Gogula T, Zou H. Copper(i)-catalyzed benzylation of triazolopyridine through direct C-H functionalization. Org Biomol Chem 2019;17:7455-60. [PMID: 31359021 DOI: 10.1039/c9ob01433k] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 2.7] [Reference Citation Analysis]
13 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]
14 Zhang Y, Teng H, Gao Y, Afzal MW, Tian J, Chen X, Tang H, James TD, Guo Y. A general strategy for selective detection of hypochlorous acid based on triazolopyridine formation. Chinese Chemical Letters 2020;31:2917-20. [DOI: 10.1016/j.cclet.2020.03.020] [Cited by in Crossref: 12] [Cited by in F6Publishing: 2] [Article Influence: 6.0] [Reference Citation Analysis]
15 Devi L, Kumar P, Kant R, Rastogi N. Exploiting the umpolung reactivity of diazo groups: direct access to triazolyl-azaarenes from azaarenes. Chem Commun (Camb) 2022;58:7062-5. [PMID: 35648386 DOI: 10.1039/d2cc01897g] [Reference Citation Analysis]
16 Yang D, Wang J, Gao P, Bai Z, Duan D, Fan M. KI-catalyzed oxidative cyclization of α-keto acids and 2-hydrazinopyridines: efficient one-pot synthesis of 1,2,4-triazolo[4,3- a ]pyridines. RSC Adv 2018;8:32597-600. [DOI: 10.1039/c8ra06215c] [Cited by in Crossref: 4] [Article Influence: 1.0] [Reference Citation Analysis]
17 Wang M, Hou J, Yu W, Chang J. Synthesis of 2 H-Azirines via Iodine-Mediated Oxidative Cyclization of Enamines. J Org Chem 2018;83:14954-61. [PMID: 30474371 DOI: 10.1021/acs.joc.8b02022] [Cited by in Crossref: 14] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
18 Wei W, Wang Z, Yang X, Yu W, Chang J. Divergent Synthesis of 1 H -Indazoles and 1 H -Pyrazoles from Hydrazones via Iodine-Mediated Intramolecular Aryl and sp3 C-H Amination. Adv Synth Catal 2017;359:3378-87. [DOI: 10.1002/adsc.201700824] [Cited by in Crossref: 18] [Cited by in F6Publishing: 6] [Article Influence: 3.6] [Reference Citation Analysis]