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For: 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: 9] [Article Influence: 3.5] [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 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]
3 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] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
4 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]
5 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: 5] [Article Influence: 4.0] [Reference Citation Analysis]
6 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] [Cited by in F6Publishing: 9] [Article Influence: 6.0] [Reference Citation Analysis]
7 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]
8 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]
9 Chen W, Liu M, Li H, Wu Y. Switchable and efficient conversion of 2-amido-aryl oxazolines to quinazolin-4(3 H )-ones and N -(2-chloroethyl)benzamides. Org Chem Front 2021;8:584-90. [DOI: 10.1039/d0qo01368d] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]