22-13: Visible-light-induced nickel-catalyzed radical cross-couplings to access α-aryl-α-trifluoromethyl alcohols

       Feng Chen, Xiu-Hua Xu, Lingling Chu and Feng-Ling Qing*    

        Org. Lett. 2022, 24, 9332−9336. DOI: 10.1021/acs.orglett.2c03943 

22-12: trans-Trifluoromethyltetrafluorosulfanyl Chloride: selective synthesis and reaction with diazo compounds

       Xin Zhao, Jia-Yi Shou, Josiah J. Newton and Feng-Ling Qing*    

        Org. Lett. 2022, 24, 8412-8416. DOI: 10.1021/acs.orglett.2c03540 

22-11: Practical synthesis of NFSI derivatives through ArSO₂NHF without F₂

       Yu-Yang Zhang, Xiu-Hua Xu and Feng-Ling Qing*    

        Chin. J. Chem. 2022, 40, 2956-2962. DOI: 10.1002/cjoc.202200537  

22-10: Three-Component Reaction of Pentafluorosulfanyl Chloride, Alkenes and Diazo Compounds and Synthesis of Pentafluorosulfanylfurans

       Jia-Yi Shou and Feng-Ling Qing*    

        Angew. Chem. Int. Ed. 2022, 61, e202208860. DOI: 10.10202/anie.202208860 

22-9: A Fruitful Decade of Organicfluorine Chemistry: New Reagents and Reactions

       Feng-Ling Qing*, Xin-Yuan Liu*, Jun-An Ma*, Qilong Shen*, Qiuling Song*, and Pingping Tang*    

        CCS Chem. 2022, 4, 2518-2549. DOI: 10.31635/ccschem.022.202201935 

22-8: The radical reaction of ethynylbenziodoxolone (EBX) reagents and pentafluorosulfanyl chloride: new approach to SF₅-substituted alkynes 

       Jia-Yi Shou, Xiu-Hua Xu and Feng-Ling Qing* 

        J. Fluorine Chem. 2022, 261-262, 110018. DOI: 10.1016/j.jfluchem.2022.110018 

22-7: Regioselective oxidative C-H heptafluoroisopropylation of heteroarenes with heptafluoroisopropyl silver

       Chao-Lai Tong, Xiu-Hua Xu and Feng-Ling Qing*    

        Org. Chem. Front. 2022, 9, 4435-4440. DOI: 10.1039/D2QO00787H  

22-6: Photoredox catalyzed difluoro(phenylthio)methylation of 2,3-allenoic acids with {difluoro(phenylthio)methyl}triphenylphosphonium triflate 

       Yao-Yao Zhu, Shuai Liu, Yangen Huang, Xiu-Hua Xu and Feng-Ling Qing* 

        J. Fluorine Chem. 2022, 257-258, 109969. DOI: 10.1016/j.jfluchem.2022.109969 

22-5: Trifluoromethylation with CF₃I and other related reagents 

       Xiu-Hua Xu and Feng-Ling Qing*   

        The Chemical Transformations of C1 Compounds. Volume 2. Chapter 36  

                 DOI: 10.1002/9783527831883.ch36

22-4: General synthesis of N-trifluoromethyl compounds with N-trifluoromethylamine hydroxyl reagents

       Shuai Liu, Yangen Huang, Juan Wang, Xiu-Hua Xu and Feng-Ling Qing*    

        J. Am. Chem. Soc. 2022, 143, 1962-1970. DOI: 10.1021/jacs.1c12467 

22-3: Photoredox catalyzed C-H trifluoroethylaminationfunction of heteroarenes

       Juan Wang, Shuai Liu, Yangen Huang, Xiu-Hua Xu and Feng-Ling Qing*    

        Chem. Commun. 2022, 58, 1346-1349. DOI: 10.1039/D1CC06688A  

22-2: Electrochemical trifluoromethoxylation of (hetero)aromatics with a trifluoromethyl source and oxygen

       Yao Ouyang, Xiu-Hua Xu and Feng-Ling Qing*    

        Angew. Chem. Int. Ed. 2022, 61, e202114048. DOI: 10.10202/anie.202114048 

22-1: Iron-catalyzed cyanoalkylation of difluoroenol silyl ethers with cyclobutanone oxime esters

       Xiao-Lei Zhu, Yangen Huang, Xiu-Hua Xu and Feng-Ling Qing*    

        Chin. Chem. Lett. 2022, 33, 817-820. DOI: 10.1016/j.cclett.2021.07.0301