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For: Wen J, Zhu L, Bi Q, Shen Z, Li X, Li X, Wang Z, Chen Z. Highly N 2 -Selective Coupling of 1,2,3-Triazoles with Indole and Pyrrole. Chem Eur J 2014;20:974-8. [DOI: 10.1002/chem.201302761] [Cited by in Crossref: 33] [Cited by in F6Publishing: 23] [Article Influence: 3.7] [Reference Citation Analysis]
Number Citing Articles
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6 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]
7 Padalkar VS, Lanke SK, Chemate SB, Sekar N. N-2-Aryl-1,2,3-Triazoles: A Novel Class of Blue Emitting Fluorophores-Synthesis, Photophysical Properties Study and DFT Computations. J Fluoresc 2015;25:985-96. [PMID: 25976087 DOI: 10.1007/s10895-015-1580-7] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 1.4] [Reference Citation Analysis]
8 Luo G, Sun C, Li Y, Li X, Zhao Z. N 2 -selective alkylation of NH-1,2,3-triazoles with vinyl ethers via gold catalysis. RSC Adv 2018;8:27610-5. [DOI: 10.1039/c8ra04790a] [Cited by in Crossref: 11] [Article Influence: 2.8] [Reference Citation Analysis]
9 Bhagat UK, Peddinti RK. Asymmetric Organocatalytic Approach to 2,4-Disubstituted 1,2,3-Triazoles by N2-Selective Aza-Michael Addition. J Org Chem 2018;83:793-804. [PMID: 29257863 DOI: 10.1021/acs.joc.7b02793] [Cited by in Crossref: 18] [Cited by in F6Publishing: 10] [Article Influence: 4.5] [Reference Citation Analysis]
10 Li Z, Wei Q, Song L, Han W, Wu X, Zhao Y, Xia F, Liu S. Highly Regioselective Radical Transformation of N -Sulfonyl-1,2,3-triazoles in Air. Org Lett 2019;21:6413-7. [DOI: 10.1021/acs.orglett.9b02269] [Cited by in Crossref: 14] [Cited by in F6Publishing: 4] [Article Influence: 4.7] [Reference Citation Analysis]
11 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]
12 Morimoto K, Ohnishi Y, Nakamura A, Sakamoto K, Dohi T, Kita Y. N1 -Selective Oxidative CN Coupling of Azoles with Pyrroles Using a Hypervalent Iodine Reagent. Asian Journal of Organic Chemistry 2014;3:382-6. [DOI: 10.1002/ajoc.201400027] [Cited by in Crossref: 19] [Cited by in F6Publishing: 12] [Article Influence: 2.4] [Reference Citation Analysis]
13 Li L, Jiang Y, Hao J, Wei Y, Shi M. N2 -Selective Autocatalytic Ditriazolylation Reactions of Cyclopropenones and Tropone with N1 -Sulfonyl-1,2,3-triazoles. Adv Synth Catal 2017;359:3304-10. [DOI: 10.1002/adsc.201700936] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 1.6] [Reference Citation Analysis]
14 Luo H, Tang Z, Wang T, Tian Y, Zhang Y, Li Y, Li S, Gong Y, Li B. Regioselective N1 - and N2 -heterocycloalkylation of N1 -sulfonyl-1,2,3-triazoles. Org Chem Front 2020;7:3727-33. [DOI: 10.1039/d0qo01111h] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
15 Hunjan MK, Panday S, Gupta A, Bhaumik J, Das P, Laha JK. Recent Advances in Functionalization of Pyrroles and their Translational Potential. Chem Rec 2021;21:715-80. [PMID: 33650751 DOI: 10.1002/tcr.202100010] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 8.0] [Reference Citation Analysis]
16 Gu C, Bi Q, Gao C, Wen J, Zhao Z, Chen Z. Post-synthetic modification of tryptophan containing peptides via NIS mediation. Org Biomol Chem 2017;15:3396-400. [DOI: 10.1039/c7ob00329c] [Cited by in Crossref: 8] [Cited by in F6Publishing: 1] [Article Influence: 1.6] [Reference Citation Analysis]
17 Yang J, He Z, Hong L, Sun W, Wang R. Asymmetric N -aminoalkylation of 3-substituted indoles by N-protected N , O -acetals: an access to chiral propargyl aminals. Org Biomol Chem 2020;18:4169-73. [DOI: 10.1039/d0ob00795a] [Cited by in Crossref: 5] [Article Influence: 2.5] [Reference Citation Analysis]
18 Shi J, Zhu L, Wen J, Chen Z. Brönsted acid catalyzed addition of N 1 - p -methyl toluenesulfonyl triazole to olefins for the preparation of N 2 -alkyl 1,2,3-triazoles with high N 2 -selectivity. Chinese Journal of Catalysis 2016;37:1222-6. [DOI: 10.1016/s1872-2067(15)61107-x] [Cited by in Crossref: 10] [Article Influence: 1.7] [Reference Citation Analysis]
19 Bao P, Meng N, Lv Y, Yue H, Li J, Wei W. Selective assembly of N 1- and N 2-alkylated 1,2,3-triazoles via copper-catalyzed decarboxylative cycloaddition of alkynyl carboxylic acids with ethers and azidotrimethylsilane. Org Chem Front 2019;6:3983-8. [DOI: 10.1039/c9qo01277j] [Cited by in Crossref: 8] [Article Influence: 2.7] [Reference Citation Analysis]
20 Xu K, Thieme N, Breit B. Unlocking the N2 Selectivity of Benzotriazoles: Regiodivergent and Highly Selective Coupling of Benzotriazoles with Allenes. Angew Chem Int Ed 2014;53:7268-71. [DOI: 10.1002/anie.201403682] [Cited by in Crossref: 91] [Cited by in F6Publishing: 76] [Article Influence: 11.4] [Reference Citation Analysis]
21 Liu H, Ding H, Zhu L, Wang Y, Chen Z, Tian Z. A Indole-Trizole-Rhodamine Triad as Ratiometric Fluorescent Probe for Nanomolar-Concentration Level Hg(2+) Sensing with High Selectivity. J Fluoresc 2015;25:1259-66. [PMID: 26179076 DOI: 10.1007/s10895-015-1614-1] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 2.1] [Reference Citation Analysis]
22 Bao P, Yue H, Meng N, Zhao X, Li J, Wei W. Copper-Catalyzed Three-Component Reaction of Alkynes, TMSN 3 , and Ethers: Regiocontrollable Synthesis of N 1 - and N 2 -Oxyalkylated 1,2,3-Triazoles. Org Lett 2019;21:7218-22. [DOI: 10.1021/acs.orglett.9b02295] [Cited by in Crossref: 17] [Cited by in F6Publishing: 5] [Article Influence: 5.7] [Reference Citation Analysis]
23 Guan C, Ji J, Li Z, Wei Q, Wu X, Liu S. Facile synthesis of N2-substituted-1,2,3-triazole from aryl ethynylene and azide via a one-pot two-step strategy. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132670] [Reference Citation Analysis]
24 Ma T, Sun C, Yuan X, Li X, Zhao Z. N-2-Selective gold-catalyzed alkylation of 1-sulfonyl-1,2,3-trizoles. RSC Adv 2017;7:1062-6. [DOI: 10.1039/c6ra26521a] [Cited by in Crossref: 13] [Article Influence: 2.6] [Reference Citation Analysis]
25 Sergeieva T, Hamlin TA, Okovytyy S, Breit B, Bickelhaupt FM. Ligand-Mediated Regioselective Rhodium-Catalyzed Benzotriazole-Allene Coupling: Mechanistic Exploration and Quantum Chemical Analysis. Chemistry 2020;26:2342-8. [PMID: 31778591 DOI: 10.1002/chem.201905359] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
26 Zhang C, Zheng L, Yan Q, Hu Q, Jia F, Chen Y. A Direct P 2 O 5 -Mediated Synthesis of Diverse Sulfur-Containing Triazoles via Alkylation of NH -1,2,3-triazoles with Dimethyl Sulfoxide. ChemistrySelect 2018;3:10277-80. [DOI: 10.1002/slct.201802875] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
27 Samanta R, Narayan R, Bauer JO, Strohmann C, Sievers S, Antonchick AP. Oxidative regioselective amination of chromones exposes potent inhibitors of the hedgehog signaling pathway. Chem Commun 2015;51:925-8. [DOI: 10.1039/c4cc08376h] [Cited by in Crossref: 36] [Cited by in F6Publishing: 2] [Article Influence: 5.1] [Reference Citation Analysis]
28 Reddy RJ, Shankar A, Waheed M, Nanubolu JB. Metal-free, highly regioselective sulfonylation of NH-1,2,3-triazoles with sodium sulfinates and thiosulfonates. Tetrahedron Letters 2018;59:2014-7. [DOI: 10.1016/j.tetlet.2018.04.023] [Cited by in Crossref: 19] [Article Influence: 4.8] [Reference Citation Analysis]
29 Zhu LL, Tian L, Cai B, Liu G, Zhang H, Wang Y. Diamine-mediated N2-selective β-selenoalkylation of triazoles with alkenes. Chem Commun (Camb) 2020;56:2979-82. [PMID: 32077882 DOI: 10.1039/d0cc00601g] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]