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For: 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]
Number Citing Articles
1 Goto M, Maejima S, Yamaguchi E, Itoh A. Regioselective Carboiodination of Styrenes: N ‐Iodosuccinimide Affords Complete Reaction Regioselectivity. Asian J Org Chem 2020;9:210-3. [DOI: 10.1002/ajoc.202000022] [Cited by in Crossref: 4] [Article Influence: 2.0] [Reference Citation Analysis]
2 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]
3 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]
4 Jannapu Reddy R, Waheed M, Karthik T, Shankar A. An efficient synthesis of 4,5-disubstituted-2 H -1,2,3-triazoles from nitroallylic derivatives via a cycloaddition–denitration process. New J Chem 2018;42:980-7. [DOI: 10.1039/c7nj03292g] [Cited by in Crossref: 20] [Article Influence: 5.0] [Reference Citation Analysis]
5 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]
6 Liu Y, Han C, Ma X, Yang J, Feng X, Jiang Y. One-pot synthesis of 1-monosubstituted-1, 2, 3-triazoles from 2-methyl-3-butyn-2-ol. Tetrahedron Letters 2018;59:650-3. [DOI: 10.1016/j.tetlet.2018.01.012] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
7 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]
8 Qian P, Du B, Song R, Wu X, Mei H, Han J, Pan Y. N -Iodosuccinimide-Initiated Spirocyclopropanation of Styrenes with 1,3-Dicarbonyl Compound for the Synthesis of Spirocyclopropanes. J Org Chem 2016;81:6546-53. [DOI: 10.1021/acs.joc.6b01163] [Cited by in Crossref: 20] [Cited by in F6Publishing: 14] [Article Influence: 3.3] [Reference Citation Analysis]
9 Singh M, Bose P, Singh AS, Tiwari VK. Synthesis of 1-(2-bromo-1-arylethyl)-1H-benzotriazoles via NBS promoted addition of 1H-benzotriazole to alkene: Relevance in benzotriazole ring cleavage. Tetrahedron 2020;76:131078. [DOI: 10.1016/j.tet.2020.131078] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
10 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]
11 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]
12 Li HH, Li XX, Zhao ZG, Yuan X, Sun CY. Regioselective 1,2-addition of allenamides with N-haloimides: synthesis of 2-halo allylic aminal derivatives. Org Biomol Chem 2017;15:4005-13. [PMID: 28443882 DOI: 10.1039/c7ob00882a] [Cited by in Crossref: 12] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
13 Huang K, Sheng G, Lu P, Wang Y. From 1-Sulfonyl-4-aryl-1,2,3-triazoles to 1-Allenyl-5-aryl-1,2,3-triazoles. J Org Chem 2017;82:5294-300. [PMID: 28474887 DOI: 10.1021/acs.joc.7b00627] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 2.4] [Reference Citation Analysis]
14 Deng X, Lei X, Nie G, Jia L, Li Y, Chen Y. Copper-Catalyzed Cross-Dehydrogenative N2-Coupling of NH-1,2,3-Triazoles with N,N -Dialkylamides: N-Amidoalkylation of NH-1,2,3-Triazoles. J Org Chem 2017;82:6163-71. [PMID: 28558242 DOI: 10.1021/acs.joc.7b00752] [Cited by in Crossref: 29] [Cited by in F6Publishing: 14] [Article Influence: 5.8] [Reference Citation Analysis]
15 Motornov VA, Tabolin AA, Novikov RA, Nelyubina YV, Ioffe SL, Smolyar IV, Nenajdenko VG. Synthesis and Regioselective N-2 Functionalization of 4-Fluoro-5-aryl-1,2,3-N H -triazoles: Synthesis and Regioselective N-2 Functionalization of 4-Fluoro-5-aryl-1,2,3-N H -triazoles. Eur J Org Chem 2017;2017:6851-60. [DOI: 10.1002/ejoc.201701338] [Cited by in Crossref: 22] [Cited by in F6Publishing: 9] [Article Influence: 4.4] [Reference Citation Analysis]
16 Re He Man XJAT, Liu YC, Li XX, Zhao ZG. Highly N2 -selective allylation of NH -1,2,3-triazoles with allenamides mediated by N -iodosuccinimide. New J Chem 2019;43:14739-46. [DOI: 10.1039/c9nj03014j] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 1.7] [Reference Citation Analysis]
17 Gupta S, Chandna N, Singh AK, Jain N. Regioselective Synthesis of N2-Alkylated-1,2,3 Triazoles and N1-Alkylated Benzotriazoles: Cu2S as a Recyclable Nanocatalyst for Oxidative Amination of N, N-Dimethylbenzylamines. J Org Chem 2018;83:3226-35. [PMID: 29463081 DOI: 10.1021/acs.joc.8b00107] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
18 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]
19 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]
20 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]
21 Peters SJ, Patel K. Electron Distribution in 1,2,3-Benzotriazole and 1,2,3-Triazole Anion Radical Isomers: An EPR and DFT Study. J Org Chem 2021;86:14786-96. [PMID: 34633818 DOI: 10.1021/acs.joc.1c01584] [Reference Citation Analysis]
22 Ma Y, Zhang X, Yang Y, Hu L, Xiong Y. Synthesis of 2-alkyl triazoles with solvothermal conditions. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132765] [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 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]
26 Payra S, Saha A, Banerjee S. On Water Cu@g‐C 3 N 4 Catalyzed Synthesis of NH‐1,2,3‐Triazoles via [2+3] Cycloadditions of Nitroolefins/Alkynes and Sodium Azide. ChemCatChem 2018;10:5468-74. [DOI: 10.1002/cctc.201801524] [Cited by in Crossref: 28] [Cited by in F6Publishing: 9] [Article Influence: 7.0] [Reference Citation Analysis]
27 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]