BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Hu S, Yang Z, Chen Z, Wu X. Metal‐Free Synthesis of 5‐Trifluoromethyl‐1,2,4‐Triazoles from Iodine‐Mediated Annulation of Trifluoroacetimidoyl Chlorides and Hydrazones. Adv Synth Catal 2019;361:4949-54. [DOI: 10.1002/adsc.201900983] [Cited by in Crossref: 22] [Cited by in F6Publishing: 8] [Article Influence: 7.3] [Reference Citation Analysis]
Number Citing Articles
1 Markos A, Janecký L, Chvojka T, Martinek T, Martinez‐seara H, Klepetářová B, Beier P. Haloalkenyl Imidoyl Halides as Multifacial Substrates in the Stereoselective Synthesis of N ‐Alkenyl Compounds. Adv Synth Catal 2021;363:3258-66. [DOI: 10.1002/adsc.202100009] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
2 Chen Z, Wang W, Yang H, Wu X. Palladium-Catalyzed Four-Component Carbonylative Cyclization Reaction of Trifluoroacetimidoyl Chlorides, Propargyl Amines, and Diaryliodonium Salts: Access to Trifluoromethyl-Containing Trisubstituted Imidazoles. Org Lett 2020;22:1980-4. [DOI: 10.1021/acs.orglett.0c00328] [Cited by in Crossref: 27] [Cited by in F6Publishing: 6] [Article Influence: 13.5] [Reference Citation Analysis]
3 Yang H, Lu SN, Chen Z, Wu XF. Silver-Mediated [3 + 2] Cycloaddition of Azomethine Ylides with Trifluoroacetimidoyl Chlorides for the Synthesis of 5-(Trifluoromethyl)imidazoles. J Org Chem 2021;86:4361-70. [PMID: 33615797 DOI: 10.1021/acs.joc.1c00131] [Cited by in Crossref: 6] [Article Influence: 6.0] [Reference Citation Analysis]
4 Matsuzaki H, Takeda N, Yasui M, Okazaki M, Suzuki S, Ueda M. Synthesis of multi-substituted 1,2,4-triazoles utilising the ambiphilic reactivity of hydrazones. Chem Commun (Camb) 2021;57:12187-90. [PMID: 34730140 DOI: 10.1039/d1cc05326d] [Reference Citation Analysis]
5 Chen Z, Wang L, Zhang J, Wu X. Palladium-catalyzed three-component carbonylative synthesis of 2-(trifluoromethyl)quinazolin-4(3 H )-ones from trifluoroacetimidoyl chlorides and amines. Org Chem Front 2020;7:2499-504. [DOI: 10.1039/d0qo00819b] [Cited by in Crossref: 19] [Cited by in F6Publishing: 6] [Article Influence: 9.5] [Reference Citation Analysis]
6 Peng X, Zhang F, Ma J. Cu‐Catalysed Three‐Component Reaction of Aryldiazonium Salts with Fluorinated Diazo Reagents and Nitriles: Access to Difluoro‐ and Trifluoromethylated N1 ‐Aryl‐1,2,4‐triazoles. Adv Synth Catal 2020;362:4432-7. [DOI: 10.1002/adsc.202000776] [Cited by in Crossref: 13] [Article Influence: 6.5] [Reference Citation Analysis]
7 Wang LC, Du S, Chen Z, Wu XF. FeCl3-Mediated Synthesis of 2-(Trifluoromethyl)quinazolin-4(3H)-ones from Isatins and Trifluoroacetimidoyl Chlorides. Org Lett 2020;22:5567-71. [PMID: 32610908 DOI: 10.1021/acs.orglett.0c01927] [Cited by in Crossref: 21] [Cited by in F6Publishing: 2] [Article Influence: 10.5] [Reference Citation Analysis]
8 Du S, Yang Z, Tang J, Chen Z, Wu XF. Synthesis of 3H-1,2,4-Triazol-3-ones via NiCl2-Promoted Cascade Annulation of Hydrazonoyl Chlorides and Sodium Cyanate. Org Lett 2021;23:2359-63. [PMID: 33691408 DOI: 10.1021/acs.orglett.1c00568] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
9 Du S, Wang WF, Song Y, Chen Z, Wu XF. Palladium-Catalyzed Cascade Carbonylative Synthesis of 1,2,4-Triazol-3-ones from Hydrazonoyl Chlorides and NaN3. Org Lett 2021;23:974-8. [PMID: 33433219 DOI: 10.1021/acs.orglett.0c04167] [Cited by in Crossref: 10] [Cited by in F6Publishing: 3] [Article Influence: 10.0] [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: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 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] [Reference Citation Analysis]
12 Song Y, Wang LC, Du S, Chen Z, Wu XF. The cascade coupling/iodoaminocyclization reaction of trifluoroacetimidoyl chlorides and allylamines: metal-free access to 2-trifluoromethyl-imidazolines. Org Biomol Chem 2021;19:6115-9. [PMID: 34165110 DOI: 10.1039/d1ob00986a] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Chen Z, Hu S, Wu X. Trifluoroacetimidoyl halides: a potent synthetic origin. Org Chem Front 2020;7:223-54. [DOI: 10.1039/c9qo01167f] [Cited by in Crossref: 21] [Article Influence: 10.5] [Reference Citation Analysis]
14 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] [Reference Citation Analysis]
15 Lv Y, Meng J, Li C, Wang X, Ye Y, Sun K. Update on the Synthesis of N‐Heterocycles via Cyclization of Hydrazones (2017–2021). Adv Synth Catal 2021;363:5235-65. [DOI: 10.1002/adsc.202101184] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Yang H, Wang L, Wang W, Chen Z, Wu X. Palladium‐Catalyzed Cascade Carbonylative Cyclization Reaction of Trifluoroacetimidoyl Chlorides and 2‐Iodoanilines: Toward 2‐(Trifluoromethyl)quinazolin‐4(3H)‐ones Synthesis. ChemistrySelect 2020;5:11072-6. [DOI: 10.1002/slct.202003269] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 3.5] [Reference Citation Analysis]
17 Wei Z, Zhang Q, Tang M, Zhang S, Zhang Q. Diversity-Oriented Synthesis of 1,2,4-Triazols, 1,3,4-Thiadiazols, and 1,3,4-Selenadiazoles from N-Tosylhydrazones. Org Lett 2021;23:4436-40. [PMID: 33988376 DOI: 10.1021/acs.orglett.1c01379] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Wang L, Zhang Y, Chen Z, Wu X. Palladium‐Catalyzed Carbonylative Synthesis of 2‐(Trifluoromethyl)quinazolin‐4(3 H )‐ones from Trifluoroacetimidoyl Chlorides and Nitro Compounds. Adv Synth Catal 2021;363:1417-26. [DOI: 10.1002/adsc.202001502] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 9.0] [Reference Citation Analysis]
19 Zhang J, Tang J, Chen Z, Wu X. Synthesis of 5‐Trifluoromethyl‐1,2,4‐Triazoles via Metal‐Free Annulation of Trifluoroacetimidohydrazides and Methyl Ketones. Adv Synth Catal 2021;363:3060-9. [DOI: 10.1002/adsc.202100130] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 5.0] [Reference Citation Analysis]
20 Yang H, Lu S, Song Y, Chen Z, Wu X. Copper-mediated [3 + 2] cycloaddition of trifluoroacetimidoyl chlorides and N -isocyanoiminotriphenylphosphorane for the synthesis of 3-trifluoromethyl-1,2,4-triazoles. Org Chem Front 2021;8:5040-4. [DOI: 10.1039/d1qo00843a] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 8.0] [Reference Citation Analysis]
21 Yavari I, Khaledian O. A formal [3+2] cycloaddition reaction of N -methylimidazole as a masked hydrogen cyanide: access to 1,3-disubstitued-1 H -1,2,4-triazoles. Chem Commun 2020;56:9150-3. [DOI: 10.1039/d0cc01065k] [Cited by in Crossref: 4] [Article Influence: 2.0] [Reference Citation Analysis]
22 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: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Hu S, Yang H, Chen Z, Wu X. Base-mediated [3+2] annulation of trifluoroacetimidoyl chlorides and isocyanides: An improved approach for regioselective synthesis of 5-trifluoromethyl-imidazoles. Tetrahedron 2020;76:131168. [DOI: 10.1016/j.tet.2020.131168] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
24 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: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
25 Abdelli A, Azzouni S, Plais R, Gaucher A, Efrit ML, Prim D. Recent advances in the chemistry of 1,2,4-triazoles: Synthesis, reactivity and biological activities. Tetrahedron Letters 2021;86:153518. [DOI: 10.1016/j.tetlet.2021.153518] [Reference Citation Analysis]
26 Yang H, Xu T, Lu S, Chen Z, Wu X. Synthesis of 5-trifluoromethyl-1,2,3-triazoles via base-mediated cascade annulation of diazo compounds with trifluoroacetimidoyl chlorides. Org Chem Front 2021;8:3440-5. [DOI: 10.1039/d1qo00445j] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 6.0] [Reference Citation Analysis]
27 Du S, Wang L, Yang Z, Chen Z, Wu X. A Convenient FeCl 3 ‐Mediated Synthesis of 5‐Trifluoromethyl‐1,2,4‐triazoles from Trifluoroacetimidoyl Chlorides and Hydrazides. Adv Synth Catal 2020;362:5130-4. [DOI: 10.1002/adsc.202001015] [Cited by in Crossref: 15] [Cited by in F6Publishing: 8] [Article Influence: 7.5] [Reference Citation Analysis]