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For: Tian Q, Chen X, Liu W, Wang Z, Shi S, Kuang C. Regioselective halogenation of 2-substituted-1,2,3-triazoles via sp2 C–H activation. Org Biomol Chem 2013;11:7830. [DOI: 10.1039/c3ob41558a] [Cited by in Crossref: 41] [Cited by in F6Publishing: 27] [Article Influence: 4.6] [Reference Citation Analysis]
Number Citing Articles
1 Kim JH, Gensch T, Zhao D, Stegemann L, Strassert CA, Glorius F. Rh III -katalysierte C-H-Aktivierung mit Pyridotriazolen: direkter Zugang zu Fluorophoren zur Metallerkennung. Angew Chem 2015;127:11126-30. [DOI: 10.1002/ange.201504757] [Cited by in Crossref: 38] [Cited by in F6Publishing: 30] [Article Influence: 5.4] [Reference Citation Analysis]
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3 Farshadfar K, Tizhoush SK, Ariafard A. Role of Brønsted Acids in Promoting Pd(OAc) 2 -Catalyzed Chlorination of Phenol Carbamates Using N -Chlorosuccinimide. ACS Catal . [DOI: 10.1021/acscatal.1c05512] [Reference Citation Analysis]
4 Hu L, Xu H, Yang Q, Deng Z, Yu C, Peng Y. Quinazoline-directed selective ortho-iodination for the synthesis of 2-(2-iodoaryl)-4-arylquinazolines. Journal of Organometallic Chemistry 2017;843:20-5. [DOI: 10.1016/j.jorganchem.2017.05.025] [Cited by in Crossref: 7] [Article Influence: 1.4] [Reference Citation Analysis]
5 Tomberg A, Muratore MÉ, Johansson MJ, Terstiege I, Sköld C, Norrby PO. Relative Strength of Common Directing Groups in Palladium-Catalyzed Aromatic C-H Activation. iScience 2019;20:373-91. [PMID: 31614320 DOI: 10.1016/j.isci.2019.09.035] [Cited by in Crossref: 20] [Cited by in F6Publishing: 13] [Article Influence: 6.7] [Reference Citation Analysis]
6 Zhang H, Yang Z, Ma Q, Liu J, Zheng Y, Guan M, Wu Y. Controlled mono-olefination versus diolefination of arenes via C–H activation in water: a key role of catalysts. Green Chem 2018;20:3140-6. [DOI: 10.1039/c8gc00790j] [Cited by in Crossref: 17] [Cited by in F6Publishing: 1] [Article Influence: 4.3] [Reference Citation Analysis]
7 Yu X, Ma Q, Lv S, Li J, Zhang C, Hai L, Wang Q, Wu Y. 1,2,3-Triazole-assisted C–H amidation by cobalt( iii ) catalysis. Org Chem Front 2017;4:2184-90. [DOI: 10.1039/c7qo00556c] [Cited by in Crossref: 26] [Article Influence: 5.2] [Reference Citation Analysis]
8 Zhao F, Liu Y, Yang S, Xie K, Jiang Y. Pd-catalyzed selective N(3)-ortho C–H arylation of 1,4-disubstituted 1,2,3-triazoles. Org Chem Front 2017;4:1112-5. [DOI: 10.1039/c6qo00834h] [Cited by in Crossref: 17] [Article Influence: 3.4] [Reference Citation Analysis]
9 Wang X, Zhang C, Li J, Jiang C, Su F, Zhan Z, Hai L, Chen Z, Wu Y. Ruthenium-catalyzed 1,2,3-triazole directed intermolecular C–H amidation of arenes with sulfonyl azides. RSC Adv 2016;6:68929-33. [DOI: 10.1039/c6ra14020c] [Cited by in Crossref: 21] [Article Influence: 3.5] [Reference Citation Analysis]
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11 Yu M, Wang Z, Tian M, Lu C, Li S, Du H. Purinyl N(3)-Directed Palladium-Catalyzed C-H Alkoxylation of N(9)-Arylpurines: A Late-Stage Strategy to Synthesize N(9)-(ortho-Alkoxyl)arylpurines. J Org Chem 2016;81:3435-42. [PMID: 27015589 DOI: 10.1021/acs.joc.6b00148] [Cited by in Crossref: 20] [Cited by in F6Publishing: 12] [Article Influence: 3.3] [Reference Citation Analysis]
12 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]
13 Shi S, Kuang C. Palladium-catalyzed ortho-alkoxylation of 2-aryl-1,2,3-triazoles. J Org Chem 2014;79:6105-12. [PMID: 24915142 DOI: 10.1021/jo5008306] [Cited by in Crossref: 81] [Cited by in F6Publishing: 65] [Article Influence: 10.1] [Reference Citation Analysis]
14 Gramage-doria R, Roisnel T. Ruthenium-Catalyzed C-H Bond Heteroarylation of Triazoles Enabled by a Deconvolution Strategy: Ruthenium-Catalyzed C-H Bond Heteroarylation of Triazoles Enabled by a Deconvolution Strategy. Eur J Org Chem 2018;2018:6083-7. [DOI: 10.1002/ejoc.201800843] [Cited by in Crossref: 3] [Article Influence: 0.8] [Reference Citation Analysis]
15 Zhao F, Chen Z, Liu Y, Xie K, Jiang Y. Palladium-Catalyzed Acylation of Arenes by 1,2,3-Triazole-Directed C-H Activation: Palladium-Catalyzed Acylation of Arenes by 1,2,3-Triazole-Directed C-H Activation. Eur J Org Chem 2016;2016:5971-9. [DOI: 10.1002/ejoc.201601061] [Cited by in Crossref: 15] [Cited by in F6Publishing: 9] [Article Influence: 2.5] [Reference Citation Analysis]
16 Zhao J, Pi C, You C, Wang Y, Cui X, Wu Y. Rhodium(III)-Catalyzed Direct C-H Alkylation of 2-Aryl-1,2,3-triazole N -Oxides with Maleimides: Rhodium(III)-Catalyzed Direct C-H Alkylation of 2-Aryl-1,2,3-triazole N -Oxides with Maleimides. Eur J Org Chem 2018;2018:6919-23. [DOI: 10.1002/ejoc.201801353] [Cited by in Crossref: 9] [Article Influence: 2.3] [Reference Citation Analysis]
17 Goitia A, Gómez-bengoa E, Correa A. Selective C(sp 2 )–H Halogenation of “Click” 4-Aryl-1,2,3-triazoles. Org Lett 2017;19:962-5. [DOI: 10.1021/acs.orglett.7b00275] [Cited by in Crossref: 28] [Cited by in F6Publishing: 16] [Article Influence: 5.6] [Reference Citation Analysis]
18 Wang Z, Kuang C. Palladium‐Catalyzed Acyloxylation of 2‐Substituted 1,2,3‐Triazoles via Direct sp2 CH Bond Activation. Adv Synth Catal 2014;356:1549-54. [DOI: 10.1002/adsc.201400096] [Cited by in Crossref: 39] [Cited by in F6Publishing: 22] [Article Influence: 4.9] [Reference Citation Analysis]
19 Sang R, Zheng Y, Zhang H, Wu X, Wang Q, Hai L, Wu Y. Palladium-catalyzed direct C–H ethoxycarbonylation of 2-aryl-1,2,3-triazoles and efficient synthesis of suvorexant. Org Chem Front 2018;5:648-52. [DOI: 10.1039/c7qo00945c] [Cited by in Crossref: 18] [Cited by in F6Publishing: 1] [Article Influence: 4.5] [Reference Citation Analysis]
20 Haito A, Yamaguchi M, Chatani N. Ru 3 (CO) 12 -Catalyzed Carbonylation of C−H Bonds by Triazole-Directed C−H Activation. Asian J Org Chem 2018;7:1315-8. [DOI: 10.1002/ajoc.201800182] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
21 Shi S, Liu W, He P, Kuang C. An easy arylation of 2-substituted 1,2,3-triazoles. Org Biomol Chem 2014;12:3576-80. [PMID: 24763600 DOI: 10.1039/c4ob00530a] [Cited by in Crossref: 25] [Cited by in F6Publishing: 16] [Article Influence: 3.1] [Reference Citation Analysis]
22 Pal P, Singh H, Panda AB, Ghosh SC. Heterogeneous Cu-MnO Catalyzed Monoselective ortho -Halogenation of Aromatic C−H Bonds under Visible Light. Asian J Org Chem 2015;4:879-83. [DOI: 10.1002/ajoc.201500245] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 2.3] [Reference Citation Analysis]
23 Petrone DA, Ye J, Lautens M. Modern Transition-Metal-Catalyzed Carbon–Halogen Bond Formation. Chem Rev 2016;116:8003-104. [DOI: 10.1021/acs.chemrev.6b00089] [Cited by in Crossref: 320] [Cited by in F6Publishing: 220] [Article Influence: 53.3] [Reference Citation Analysis]
24 Guerrero I, Correa A. Metal-Catalyzed C-H Functionalization Processes with “Click”-Triazole Assistance: Metal-Catalyzed C-H Functionalization Processes with “Click”-Triazole Assistance. Eur J Org Chem 2018;2018:6034-49. [DOI: 10.1002/ejoc.201800790] [Cited by in Crossref: 17] [Cited by in F6Publishing: 9] [Article Influence: 4.3] [Reference Citation Analysis]
25 Zhang H, Jing L, Zheng Y, Sang R, Zhao Y, Wang Q, Wu Y. Rhodium-Catalyzed ortho -Cyanation of 2-Aryl-1,2,3-triazole: An Alternative Approach to Suvorexant: Rhodium-Catalyzed ortho -Cyanation of 2-Aryl-1,2,3-triazole: An Alternative Approach to Suvorexant. Eur J Org Chem 2018;2018:723-9. [DOI: 10.1002/ejoc.201701476] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
26 Erbing E, Sanz-marco A, Vázquez-romero A, Malmberg J, Johansson MJ, Gómez-bengoa E, Martín-matute B. Base- and Additive-Free Ir-Catalyzed ortho -Iodination of Benzoic Acids: Scope and Mechanistic Investigations. ACS Catal 2018;8:920-5. [DOI: 10.1021/acscatal.7b02987] [Cited by in Crossref: 33] [Cited by in F6Publishing: 15] [Article Influence: 8.3] [Reference Citation Analysis]
27 Xiong X, Tan F, Yeung Y. Zwitterionic-Salt-Catalyzed Site-Selective Monobromination of Arenes. Org Lett 2017;19:4243-6. [DOI: 10.1021/acs.orglett.7b01899] [Cited by in Crossref: 28] [Cited by in F6Publishing: 19] [Article Influence: 5.6] [Reference Citation Analysis]
28 Ma X, Mo Q, Chang J, Xie K. Pd-catalyzed regioselective C-H chlorination of disubstituted 1,2,3-triazoles. Synthetic Communications 2018;48:1403-12. [DOI: 10.1080/00397911.2018.1455872] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
29 Hong X, Zhou Q, Huang S, Cui H, Li Z, Hou X. Transition metal catalysed C7 and ortho -selective halogenation of 2-arylbenzo[ d ]oxazoles. Org Chem Front 2019;6:2226-33. [DOI: 10.1039/c9qo00429g] [Cited by in Crossref: 8] [Article Influence: 2.7] [Reference Citation Analysis]
30 Saito H, Yamamoto K, Sumiya Y, Liu L, Nogi K, Maeda S, Yorimitsu H. Palladium‐Catalyzed C−H Iodination of Arenes by Means of Sulfinyl Directing Groups. Chem Asian J 2020;15:2442-6. [DOI: 10.1002/asia.202000591] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
31 Premi C, Patel SS, Jain N. Regioselective ortho -Acylation of N -Aryl-1,2,3-triazoles with Alcohols in Water: Regioselective ortho -Acylation of N -Aryl-1,2,3-triazoles with Alcohols in Water. Eur J Org Chem 2016;2016:3788-95. [DOI: 10.1002/ejoc.201600479] [Cited by in Crossref: 12] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
32 Li J, Cong W, Gao Z, Zhang J, Yang H, Jiang G. Rh( iii )-Catalyzed regioselective mono- and di-iodination of azobenzenes using alkyl iodide. Org Biomol Chem 2018;16:3479-86. [DOI: 10.1039/c8ob00318a] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
33 Kim JH, Gensch T, Zhao D, Stegemann L, Strassert CA, Glorius F. Rh III -Catalyzed CH Activation with Pyridotriazoles: Direct Access to Fluorophores for Metal-Ion Detection. Angew Chem Int Ed 2015;54:10975-9. [DOI: 10.1002/anie.201504757] [Cited by in Crossref: 100] [Cited by in F6Publishing: 80] [Article Influence: 14.3] [Reference Citation Analysis]
34 Wirtanen T, Rodrigo E, Waldvogel SR. Selective and Scalable Electrosynthesis of 2H-2-(Aryl)-benzo[d]-1,2,3-triazoles and Their N-Oxides by Using Leaded Bronze Cathodes. Chemistry 2020;26:5592-7. [PMID: 31995654 DOI: 10.1002/chem.201905874] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 2.5] [Reference Citation Analysis]
35 Liu Y, Yang J, Ma X, Han C, Jiang Y. Metal-Free Synthesis of Etherified 3-(1 H -1,2,3-Triazol-1-yl)phenyl Iodides through O-H Arylation/C-H Iodination with Diacetoxyiodobenzenes: Metal-Free Synthesis of Etherified 3-(1 H -1,2,3-Triazol-1-yl)phenyl Iodides through O-H Arylation/C-H Iodination with Diacetoxyiodobenzenes. Eur J Org Chem 2017;2017:5769-75. [DOI: 10.1002/ejoc.201701114] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]