Fluorine Synthetic and Medicinal Research Group
17. Liu, Q.; Qin, C.; Wan, J.; Bin, K.; Kobayashi, H.; Zahedian, H.; Liu, P.; Hoveyda, A. H. Synthesis of Z-gem-Cl,CF3-Substituted Alkenes by Stereoselective Cross-Metathesis and the Role of Disubstituted Mo Alkylidenes.
J. Am. Chem. Soc. 2024, accepted
16. Amir H. Hoveyda, Can Qin, Xin Zhi Sui, Qinghe Liu, Xinghan Li, and Ali Nikbakht. Taking Olefin Metathesis to the Limit: Stereocontrolled Synthesis of Trisubstituted Alkenes
Acc. Chem. Res. 2023, 56, 18, 2426.
Prior to CPU:
16. 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)
15. 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)
14. 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 Chem. 2022, Accepted.
DOI: doi.org/10.31635/ccschem.022.202101634
13. 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)
12. 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)
11. 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)
10. 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)
9. 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, doi.org/10.1002/anie.202208742. (IF: 16.8) )
8. 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)
7. 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)
6. 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)
5. 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)
4. 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)
3. 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)
2. 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)
1. 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)