Fluorine Synthetic and Medicinal Research Group
15. Liu, Q.; Mu, Y.; Koengeter, T.; Schrock, R.; Hoveyda, A. H.* Stereodefined alkenes with a fluoro-chloro terminus as a uniquely enabling compound class.
Nature Chem. 2022, 14, 463. (IF: 24.3)
14. Liu, Q. #; Ni, C. #; Hu, J.* China's flourishing synthetic organofluorine chemistry: innovations in the new millennium.
Natl. Sci. Rev. 2017, 4, 303. (IF: 23.2)
13. Liu, Q.; Ni, C.; Wang, Q.; Meng, D.; Hu, J.* Difluoromethyl 2-pyridyl sulfoximine: a stereoselective nucleophilic reagent for difluoro(aminosulfinyl)methylation and difluoro(aminosulfonyl)methylation.
CCS Chemistry 2022, Accepted.
DOI: doi.org/10.31635/ccschem.022.202101634
12. Liu, Q.; Shen, X.; Ni, C.; Hu, J.* Stereoselective carbonyl olefination with fluorosulfoximines: facile access to Z or E terminal monofluoroalkenes.
Angew. Chem. Int. Ed. 2017, 56, 619. (IF: 16.8)
11. Wang, X. #;Zhou, M. #; Liu, Q. #;Ni, C.; Fei, Z.; Li, W.; Hu, J.* Deoxyfluorination of alcohols with aryl fluorosulfonates.
Chem. Commun. 2021, 4, 303. (IF: 6.1)
10. Liu, Q.; Kong, T.; Ni, C.; Hu, J.* Dynamic kinetic resolution enabled highly stereoselective nucleophilic fluoroalkylation to access chiral b-fluoro amines.
Org. Lett. 2022, 24, 5982. (IF: 6.0)
9. Liu, Q.; Kong, T.; Ni, C.; Hu, J.* Reagent-Controlled Highly Stereoselective Difluoromethylation: Efficient Access to Chiral a-Difluoromethylamines from Ketimines. Molecules 2022, 27, 7076. (IF: 4.9)
8. Liu, Q.; Gao, Y.; Guo, M.; Li, G.* A novel manganese(II) coordination polymer built by thiourea-based carboxylate ligand.
Synth. React. Inorg. Met-Org. Chem. 2011, 41, 958. (Currently known as Inorganic and Nano-Metal Chemistry)
9. Koengeter, T.; Qin, C.; Mai, B. K.; Liu, Q.; Mu, Y.; Liu, P.; Hoveyda, A. H.* Catalytic Cross-Metathesis Reactions that Afford E- and Z-Trisubstituted Alkenyl Bromides. Scope, Applications, Mechanistic Insights. J. Am. Chem. Soc. 2023, 145, 3774-3785. (IF: 16.3)
10. Wang, Q.; Ni, C.; Hu, M.; Xie, Q.; Liu, Q.; Pan, S.; Hu, J.* From C1 to C3: copper-catalyzed gem-bis(trifluoromethyl)olefination of α-diazo esters with TMSCF3. Angew. Chem. Int. Ed. 2020, 59, 8507. (IF: 16.8)
11. Akiyama, S.; Kubota, K.; Mikus, M. S.; Paioti, P. H. S.; Romiti, F.; Liu, Q.; Zhou, Y.; Hoveyda, A. H.*; Ito, H.* Catalytic enantioselective synthesis of allylic boronates bearing a trisubstituted alkenyl fluoride and related derivatives. Angew. Chem. Int. Ed. 2019, 58, 11998. (IF: 16.8)
12. Paioti, P. H. S.; Fager, D.; Xu, S.; Liu, Q.; Hoveyda, A. H.* Commercially available organofluorine compounds as convenient launching points for stereocontrolled synthesis of more complex derivatives. Angew. Chem. Int. Ed. 2022, accepted. (IF: 16.8) (doi.org/10.1002/anie.202208742)
13. Shen, X.; Liu, Q.; Luo, T.; Hu, J.* Nucleophilic difluoromethylation of epoxides with PhSO(NTBS)CF2H by a preorganization strategy. Chem. Eur. J. 2014, 20, 6795. (IF: 5.0)
14. Shen, X.; Liu, Q.; Zhang, W.; Hu, J.* Stereoselective synthesis of (sulfonimidoyl)cyclopropanes with (R)-PhSO(NTs)CH2Cl and a,b-unsaturated Weinreb amides: tuning the of selectivity between C-Cl and C-S bond cleavage. Eur. J. Org. Chem. 2016, 906. (IF: 3.3)
15. Shen, X.; Liu, Q.; Ni, C.; Hu, J.* Nucleophilic difluoro(phenylsulfonimidoyl)methylation of unactivated alkyl bromides with PhSO(NTBS)CF2H: facile entry into gem-difluoroalkenes. Chin. J. Chem. 2014, 32, 703. (IF: 5.6)
16. Gao, Y.; Liu, Q.; Zhang, F.; Li, G.*; Wang, W.; Lu, H. Three main group metal coordination polymers bearing imidazole-based dicarboxylates: hydro(solvo)thermal syntheses, crystal structures and properties. Polyhedron 2011, 30, 1. (IF: 3.3)