BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Zhu C, Zeng H, Chen F, Liu C, Zhu R, Wu W, Jiang H. Copper-catalyzed coupling of oxime acetates and aryldiazonium salts: an azide-free strategy toward N -2-aryl-1,2,3-triazoles. Org Chem Front 2018;5:571-6. [DOI: 10.1039/c7qo00874k] [Cited by in Crossref: 35] [Cited by in F6Publishing: 1] [Article Influence: 8.8] [Reference Citation Analysis]
Number Citing Articles
1 Baidya M, Mallick S, De Sarkar S. Regioselective Synthesis of N2-Aryl 1,2,3-Triazoles via Electro-oxidative Coupling of Enamines and Aryldiazonium Salts. Org Lett 2022. [PMID: 35112868 DOI: 10.1021/acs.orglett.1c04099] [Reference Citation Analysis]
2 Xie R, Liu J, Zhang Q, Yang Y, Song L, Shao T, Liu K, Zhu Y. Copper-catalyzed aerobic oxidative domino cyclization of methyl azaarenes with 6-amino-pyrimidine-2,4-diones and pyrazol-5-amines: access to dipyrimidine/dipyrazolo-fused pyridines. Org Chem Front 2021;8:2274-9. [DOI: 10.1039/d0qo01588a] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 7.0] [Reference Citation Analysis]
3 Tian Y, Zhang F, Nie J, Cheung CW, Ma J. Metal‐free Decarboxylative Annulation of 2‐Aryl‐2‐isocyano‐acetates with Aryldiazonium Salts: General Access to 1,3‐Diaryl‐1,2,4‐triazoles. Adv Synth Catal 2021;363:227-33. [DOI: 10.1002/adsc.202001016] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
4 Liu YY, Wei Y, Huang ZH, Liu Y. Mild and efficient copper-catalyzed oxidative cyclization of oximes with 2-aminobenzyl alcohols at room temperature: synthesis of polysubstituted quinolines. Org Biomol Chem 2021;19:659-66. [PMID: 33399162 DOI: 10.1039/d0ob02348e] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Ramaraju A, Upare A, Blanch EW, Maniam S, Sridhar B, Bathula SR, Raji Reddy C. Chemoselective [3 + 2] annulation of oxime acetate with 2-aryl-3-ethoxycarbonyl-pyrroline-4,5-dione: an entry to pyrrolo[2,3-b]pyrrole derivatives. Org Biomol Chem 2021;19:7875-82. [PMID: 34549208 DOI: 10.1039/d1ob00990g] [Reference Citation Analysis]
6 Fu Y, Zhao X, Chen D, Luo J, Huang S. Cu-catalyzed coupling of indanone oxime acetates with thiols to 2,3-difunctionalized indenones. Chem Commun (Camb) 2021;57:10719-22. [PMID: 34581714 DOI: 10.1039/d1cc04167c] [Reference Citation Analysis]
7 Zhu C, Zeng H, Chen F, Liu C, Jiang H. Copper‐Catalyzed Cyclization of Aryl Amines and Aryldiazonium Salts under Air: Access to N ‐2‐Aryl‐Naphthotriazoles. Adv Synth Catal 2019;361:5149-59. [DOI: 10.1002/adsc.201900981] [Cited by in Crossref: 8] [Article Influence: 2.7] [Reference Citation Analysis]
8 Ni J, Mao X, Zhang A. Copper‐Catalyzed Synthesis of gem ‐Bisarylthio Enamines under Redox‐Neutral Conditions. Adv Synth Catal 2019;361:2004-8. [DOI: 10.1002/adsc.201900035] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 2.3] [Reference Citation Analysis]
9 Huang Y, Chen D, Zheng Y, Huang S. Synthesis of 3‐Sulfonyl Indenones via Copper‐Catalyzed Redox‐Neutral Coupling Reaction. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202104347] [Reference Citation Analysis]
10 Zhang X, Pan Y, Wang H, Liang C, Ma X, Jiao W, Shao H. Strategy to Construct 1,2,3‐Triazoles by K 2 CO 3 ‐Mediated [4+1] Annulation Reactions of N ‐Acetyl Hydrazones with Bifunctional Amino Reagents. Adv Synth Catal 2021;363:459-63. [DOI: 10.1002/adsc.202001375] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Miao CB, Guan HR, Tang Y, Wang K, Ren WL, Lyu X, Yao C, Yang HT. Copper-Catalyzed Bisannulations of Malonate-Tethered O-Acyl Oximes with Pyridine, Pyrazine, Pyridazine, and Quinoline Derivatives for the Construction of Dihydroindolizine-Fused Pyrrolidinones and Analogues. Org Lett 2021;23:8699-704. [PMID: 34723547 DOI: 10.1021/acs.orglett.1c03078] [Reference Citation Analysis]
12 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]
13 Zhu C, Zeng H, Chen F, Yang Z, Cai Y, Jiang H. Intermolecular C(sp 3 )−H Amination Promoted by Internal Oxidants: Synthesis of Trifluoroacetylated Hydrazones. Angew Chem 2018;130:17461-5. [DOI: 10.1002/ange.201810502] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
14 Wu P, He Y, Wang H, Zhou Y, Yu Z. Copper(II)-Catalyzed C–H Nitrogenation/Annulation Cascade of Ketene N , S -Acetals with Aryldiazonium Salts: A Direct Access to N2 -Substituted Triazole and Triazine Derivatives. Org Lett 2020;22:310-5. [DOI: 10.1021/acs.orglett.9b04335] [Cited by in Crossref: 14] [Article Influence: 4.7] [Reference Citation Analysis]
15 Feng FF, Li JK, Liu XY, Zhang FG, Cheung CW, Ma JA. General Synthesis of Tri-Carbo-Substituted N2-Aryl-1,2,3-triazoles via Cu-Catalyzed Annulation of Azirines with Aryldiazonium Salts. J Org Chem 2020;85:10872-83. [PMID: 32691600 DOI: 10.1021/acs.joc.0c01433] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]