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For: Ueda S, Su M, Buchwald SL. Highly N2-selective palladium-catalyzed arylation of 1,2,3-triazoles. Angew Chem Int Ed Engl 2011;50:8944-7. [PMID: 21853510 DOI: 10.1002/anie.201103882] [Cited by in Crossref: 116] [Cited by in F6Publishing: 88] [Article Influence: 10.5] [Reference Citation Analysis]
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11 Ueda S, Ali S, Fors BP, Buchwald SL. Me3(OMe)tBuXPhos: a surrogate ligand for Me4tBuXPhos in palladium-catalyzed C-N and C-O bond-forming reactions. J Org Chem 2012;77:2543-7. [PMID: 22313416 DOI: 10.1021/jo202537e] [Cited by in Crossref: 40] [Cited by in F6Publishing: 33] [Article Influence: 4.0] [Reference Citation Analysis]
12 Guru MM, Punniyamurthy T. Copper(II)-Catalyzed Aerobic Oxidative Synthesis of Substituted 1,2,3- and 1,2,4-Triazoles from Bisarylhydrazones via C–H Functionalization/C–C/N–N/C–N Bonds Formation. J Org Chem 2012;77:5063-73. [DOI: 10.1021/jo300592t] [Cited by in Crossref: 87] [Cited by in F6Publishing: 61] [Article Influence: 8.7] [Reference Citation Analysis]
13 Zhu L, Xu X, Shi J, Chen B, Chen Z. N2 -Selective Iodofunctionalization of Olefins with NH -1,2,3-Triazoles to provide N2 -Alkyl-Substituted 1,2,3-Triazoles. J Org Chem 2016;81:3568-75. [DOI: 10.1021/acs.joc.6b00185] [Cited by in Crossref: 32] [Cited by in F6Publishing: 15] [Article Influence: 5.3] [Reference Citation Analysis]
14 Wei H, Hu Q, Ma Y, Wei L, Liu J, Shi M, Wang F. Highly N 2 -Regioselective TsOH-Catalyzed Olefin Hydroamination: Metal-Free Synthesis of N2 -Alkyl-1,2,3-triazoles. Asian J Org Chem 2017;6:662-5. [DOI: 10.1002/ajoc.201700045] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
15 Kang T, Kim H, Lee D. Triazoliptycenes: A Twist on Iptycene Chemistry for Regioselective Cross-Coupling To Build Nonstacking Fluorophores. Org Lett 2017;19:6380-3. [PMID: 29144765 DOI: 10.1021/acs.orglett.7b03239] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 1.6] [Reference Citation Analysis]
16 Xu K, Thieme N, Breit B. Unlocking the N2 Selectivity of Benzotriazoles: Regiodivergent and Highly Selective Coupling of Benzotriazoles with Allenes. Angew Chem 2014;126:7396-9. [DOI: 10.1002/ange.201403682] [Cited by in Crossref: 46] [Cited by in F6Publishing: 40] [Article Influence: 5.8] [Reference Citation Analysis]
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20 Rao DN, Rasheed S, Kumar KA, Reddy AS, Das P. Copper-Catalyzed CNH 2 Arylation of 2-Aminobenzimidazoles and Related C-Amino-NH-azoles. Adv Synth Catal 2016;358:2126-33. [DOI: 10.1002/adsc.201600035] [Cited by in Crossref: 30] [Cited by in F6Publishing: 20] [Article Influence: 5.0] [Reference Citation Analysis]
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23 Chen H, Yi H, Tang Z, Bian C, Zhang H, Lei A. External Oxidant-Free Regioselective Cross Dehydrogenative Coupling of 2-Arylimidazoheterocycles and Azoles with H 2 Evolution via Photoredox Catalysis. Adv Synth Catal 2018;360:3220-7. [DOI: 10.1002/adsc.201800531] [Cited by in Crossref: 34] [Cited by in F6Publishing: 20] [Article Influence: 8.5] [Reference Citation Analysis]
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26 Jacq J, Pasau P. Multistep Flow Synthesis of 5-Amino-2-aryl-2 H -[1,2,3]-triazole-4-carbonitriles. Chem Eur J 2014;20:12223-33. [DOI: 10.1002/chem.201402074] [Cited by in Crossref: 15] [Cited by in F6Publishing: 12] [Article Influence: 1.9] [Reference Citation Analysis]
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28 Ryu T, Min J, Choi W, Jeon WH, Lee PH. Synthesis of 2-Aryl-2 H -benzotrizoles from Azobenzenes and N -Sulfonyl Azides through Sequential Rhodium-Catalyzed Amidation and Oxidation in One Pot. Org Lett 2014;16:2810-3. [DOI: 10.1021/ol501250t] [Cited by in Crossref: 91] [Cited by in F6Publishing: 70] [Article Influence: 11.4] [Reference Citation Analysis]
29 Shi S, Buchwald SL. Palladium-Catalyzed Intramolecular CH Difluoroalkylation: Synthesis of Substituted 3,3-Difluoro-2-oxindoles. Angew Chem 2015;127:1666-70. [DOI: 10.1002/ange.201410471] [Cited by in Crossref: 25] [Cited by in F6Publishing: 22] [Article Influence: 3.1] [Reference Citation Analysis]
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31 Nagaradja E, Bentabed-Ababsa G, Scalabrini M, Chevallier F, Philippot S, Fontanay S, Duval RE, Halauko YS, Ivashkevich OA, Matulis VE, Roisnel T, Mongin F. Deprotometalation-iodolysis and computed CH acidity of 1,2,3- and 1,2,4-triazoles. Application to the synthesis of resveratrol analogues. Bioorg Med Chem 2015;23:6355-63. [PMID: 26344592 DOI: 10.1016/j.bmc.2015.08.031] [Cited by in Crossref: 18] [Cited by in F6Publishing: 12] [Article Influence: 2.6] [Reference Citation Analysis]
32 Wu L, Guo S, Wang X, Guo Z, Yao G, Lin Q, Wu M. Tandem synthesis of 2-aryl-1,2,3-triazoles from α-arylhydrazonoketones with NH4OAc via copper-catalyzed aerobic oxidation. Tetrahedron Letters 2015;56:2145-8. [DOI: 10.1016/j.tetlet.2015.03.019] [Cited by in Crossref: 24] [Cited by in F6Publishing: 11] [Article Influence: 3.4] [Reference Citation Analysis]
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34 Jankovič D, Virant M, Gazvoda M. Copper-Catalyzed Azide-Alkyne Cycloaddition of Hydrazoic Acid Formed In Situ from Sodium Azide Affords 4-Monosubstituted-1,2,3-Triazoles. J Org Chem 2022. [PMID: 35148087 DOI: 10.1021/acs.joc.1c02775] [Reference Citation Analysis]
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36 Tang J, Ming L, Zhao X. Highly Efficient Cycloaddition Reaction of 1,3-Diynes with Sodium Azide: A New Way to 5-Substituted-4-acetylene-1 H -1,2,3-triazoles: Highly Efficient Cycloaddition Reaction of 1,3-Diynes with Sodium Azide: A New Way to 5-Substituted-4-acetylene-1 H -1,2,3-triazoles. J Heterocyclic Chem 2016;53:1367-70. [DOI: 10.1002/jhet.1950] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
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41 Liang J, Rao Y, Zhu W, Wen T, Huang J, Chen Z, Chen L, Li Y, Chen X, Zhu Z. AgNO3 as Nitrogen Source for Cu-Catalyzed Cyclization of Oximes with Isocyanates: A Facile Route to N-2-Aryl-1,2,3-triazoles. Org Lett 2021;23:7028-32. [PMID: 34459610 DOI: 10.1021/acs.orglett.1c02323] [Reference Citation Analysis]
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