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For: 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: 12] [Article Influence: 9.0] [Reference Citation Analysis]
Number Citing Articles
1 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]
2 Sun Y, Yang Z, Lu SN, Chen Z, Wu XF. Formal [4+1] Annulation of Azoalkenes with CF3-Imidoyl Sulfoxonium Ylides and Dual Double Bond Isomerization Cascade: Synthesis of Trifluoromethyl-Containing Pyrazole Derivatives. Org Lett 2022. [PMID: 36082936 DOI: 10.1021/acs.orglett.2c02746] [Reference Citation Analysis]
3 Arun R, Stiniya S, Saranya PV, Anilkumar G. An Overview of Palladium-catalyzed Trifluoromethylation Reactions. Journal of Organometallic Chemistry 2022. [DOI: 10.1016/j.jorganchem.2022.122492] [Reference Citation Analysis]
4 Tang J, Yang Z, Song Y, Chen Z, Wu X. Palladium-catalyzed norbornene-mediated dehydrogenative annulation of 3-iodochromones with trifluoroacetimidoyl chlorides for the construction of trifluoromethyl-substituted chromeno[2,3-c]quinolin-12-ones. Molecular Catalysis 2022;524:112320. [DOI: 10.1016/j.mcat.2022.112320] [Reference Citation Analysis]
5 Feng Z, Ma J, Cheung CW. Ni-Catalysed intramolecular reductive aminocarbonylation of 2-haloaryl-tethered nitroarenes for the synthesis of dibenzazepine-based heterocycles. Org Chem Front . [DOI: 10.1039/d2qo00699e] [Reference Citation Analysis]
6 Yang H, Zhang J, Chen Z, Wu XF. TFBen (Benzene-1,3,5-triyl triformate): A Powerful and Versatile CO Surrogate. Chem Rec 2021. [PMID: 34591367 DOI: 10.1002/tcr.202100220] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
7 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] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
8 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: 7] [Article Influence: 5.0] [Reference Citation Analysis]
9 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: 3] [Article Influence: 3.0] [Reference Citation Analysis]
10 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: 7] [Article Influence: 8.0] [Reference Citation Analysis]
11 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: 6] [Cited by in F6Publishing: 9] [Article Influence: 6.0] [Reference Citation Analysis]
12 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: 5] [Article Influence: 6.0] [Reference Citation Analysis]