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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 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]
2 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]
3 Hu W, Pi C, Hu D, Han X, Wu Y, Cui X. Rh(III)-Catalyzed Synthesis of Indazolo[2,3-a]quinolines: Vinylene Carbonate as C1 and C2 Building Blocks. Org Lett 2022. [PMID: 35377649 DOI: 10.1021/acs.orglett.2c00580] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 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]
5 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]