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For: Zhang J, Xu T, Chen Z, Wu X. Metal-free oxidative cyclization of trifluoroacetimidohydrazides with methylhetarenes: a facile access to 3-hetaryl-5-trifluoromethyl-1,2,4-triazoles. Org Chem Front 2021;8:4490-5. [DOI: 10.1039/d1qo00790d] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 12.0] [Reference Citation Analysis]
Number Citing Articles
1 Lin B, Zhang Z, Yao Y, You Y, Weng Z. Regioselective Synthesis of 5-Trifluoromethyl 1,2,4-Triazoles via [3 + 2]-Cycloaddition of Nitrile Imines with CF3CN. Molecules 2022;27:6568. [PMID: 36235104 DOI: 10.3390/molecules27196568] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
2 Wang B, Sun Y, Cheng A, Zhu Y, Wang J, Chen Z, Wu X. Metal-free synthesis of 3-trifluoromethyl-1,2,4-triazoles via multi-component reaction of trifluoroacetimidoyl chlorides, hydrazine hydrate and benzene-1,3,5-triyl triformate. Front Chem 2022;10:1013977. [DOI: 10.3389/fchem.2022.1013977] [Reference Citation Analysis]
3 Zhu YP, Zhou Y, Li WJ, Liu FR, Wang WC, Hao KY, Chao BY, Shi TR, Wu AX, Sun YY. Iodine-Promoted Oxidative Cyclization of Methyl Azaarenes and α-Amino Ketones for One-Pot Synthesis of 2-Azaaryl-5-aryl Oxazoles. J Org Chem 2022. [PMID: 36067376 DOI: 10.1021/acs.joc.2c01399] [Reference Citation Analysis]
4 Zhang Y, Wei G, Qiu S, Chen Z, Wu X. Heating-induced decarboxylative cyclization for the synthesis of 5-trifluoromethyl-1,2,4-triazoles from trifluoroacetimidohydrazides and α-oxocarboxylic acids. Green Synthesis and Catalysis 2022. [DOI: 10.1016/j.gresc.2022.08.001] [Reference Citation Analysis]
5 Lu S, Zhang J, Li J, Chen Z, Wu X. Metal-free synthesis of 3-trifluoromethyl-1,2,4-triazoles via oxidative cyclization of trifluoroacetimidohydrazides with N,N-dimethylformamide as carbon synthons. Green Synthesis and Catalysis 2022. [DOI: 10.1016/j.gresc.2022.06.007] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Lu S, Sun Y, Zhang J, Chen Z, Wu X. Metal-free Synthesis of 5-Trifluoromethyl-1,2,4-triazoles via elemental sulfur promoted oxidative cyclization of trifluoroacetimidohydrazides with benzylic and aliphatic amines. Molecular Catalysis 2022;524:112336. [DOI: 10.1016/j.mcat.2022.112336] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Liu X, Liu H, Bian C, Wang KH, Wang J, Huang D, Su Y, Lv X, Hu Y. Synthesis of 3-Trifluoromethyl-1,2,4-triazolines and 1,2,4-Triazoles via Tandem Addition/Cyclization of Trifluoromethyl N-Acylhydrazones with Cyanamide. J Org Chem 2022. [PMID: 35412831 DOI: 10.1021/acs.joc.2c00176] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
8 Kamal R, Omkar, Kumar V, Kumar R. Hydroxy(tosyloxy)iodobenzene (HTIB): A Convenient Oxidizing Agent for the Synthesis of Heterocycles. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202103719] [Reference Citation Analysis]
9 Zhang J, Tang J, Chen Z, Wu X. Elemental Sulfur and Dimethyl Sulfoxide‐Promoted Oxidative Cyclization of Trifluoroacetimidohydrazides with Methylhetarenes for the Synthesis of 3‐Hetaryl ‐5‐trifluoromethyl‐1,2,4‐triazoles. Chin J Chem 2021;39:3443-7. [DOI: 10.1002/cjoc.202100579] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 6.0] [Reference Citation Analysis]
10 Lu S, Yang H, Zhang J, Chen Z, Wu X. Oxidative Cyclization of Trifluoroacetimidohydrazides with D‐Glucose for the Metal‐Free Synthesis of 3‐Trifluoromethyl‐1,2,4‐Triazoles. Adv Synth Catal 2021;363:4982-7. [DOI: 10.1002/adsc.202100989] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
11 Tang J, Zhang J, Zhang Y, Chen Z, Wu X. Palladium-catalyzed carbonylative synthesis of 5-trifluoromethyl-1,2,4-triazoles from trifluoroacetimidohydrazides and aryl iodides. Org Chem Front 2021;8:6089-94. [DOI: 10.1039/d1qo01064f] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]