| Year |
Citation |
Score |
| 2023 |
Hoveyda AH, Qin C, Sui XZ, Liu Q, Li X, Nikbakht A. Taking Olefin Metathesis to the Limit: Stereocontrolled Synthesis of Trisubstituted Alkenes. Accounts of Chemical Research. PMID 37643361 DOI: 10.1021/acs.accounts.3c00341 |
0.595 |
|
| 2023 |
Koengeter T, Qin C, Mai BK, Liu Q, Mu Y, Liu P, Hoveyda AH. Catalytic Cross-Metathesis Reactions That Afford - and -Trisubstituted Alkenyl Bromides: Scope, Applications, and Mechanistic Insights. Journal of the American Chemical Society. PMID 36724200 DOI: 10.1021/jacs.2c13289 |
0.616 |
|
| 2022 |
Liu Q, Kong T, Ni C, Hu J. Reagent-Controlled Highly Stereoselective Difluoromethylation: Efficient Access to Chiral α-Difluoromethylamines from Ketimines. Molecules (Basel, Switzerland). 27. PMID 36296670 DOI: 10.3390/molecules27207076 |
0.563 |
|
| 2022 |
Paioti PHS, Gonsales SA, Xu S, Nikbakht A, Fager DC, Liu Q, Hoveyda AH. Catalytic and Stereoselective Transformations with Easily Accessible and Purchasable Allyl and Alkenyl Fluorides. Angewandte Chemie (International Ed. in English). PMID 36017964 DOI: 10.1002/anie.202208742 |
0.673 |
|
| 2022 |
Liu Q, Kong T, Ni C, Hu J. Dynamic Kinetic Resolution-Enabled Highly Stereoselective Nucleophilic Fluoroalkylation to Access Chiral β-Fluoro Amines. Organic Letters. PMID 35939038 DOI: 10.1021/acs.orglett.2c02250 |
0.55 |
|
| 2022 |
Liu Q, Mu Y, Koengeter T, Schrock RR, Hoveyda AH. Publisher Correction: Stereodefined alkenes with a fluoro-chloro terminus as a uniquely enabling compound class. Nature Chemistry. 14: 474. PMID 35332285 DOI: 10.1038/s41557-022-00930-3 |
0.439 |
|
| 2022 |
Liu Q, Mu Y, Koengeter T, Schrock RR, Hoveyda AH. Stereodefined alkenes with a fluoro-chloro terminus as a uniquely enabling compound class. Nature Chemistry. PMID 35177787 DOI: 10.1038/s41557-022-00893-5 |
0.532 |
|
| 2021 |
Wang X, Zhou M, Liu Q, Ni C, Fei Z, Li W, Hu J. Deoxyfluorination of alcohols with aryl fluorosulfonates. Chemical Communications (Cambridge, England). PMID 34318800 DOI: 10.1039/d1cc02617h |
0.524 |
|
| 2020 |
Hu J, Wang Q, Ni C, Hu M, Xie Q, Liu Q, Pan S. From C1 to C3: Copper-Catalyzed gem-Bis(trifluoromethyl)olefination of α-Diazo Esters with TMSCF3. Angewandte Chemie (International Ed. in English). PMID 32119159 DOI: 10.1002/Anie.202002409 |
0.669 |
|
| 2019 |
Akiyama S, Kubota K, Mikus MS, Paioti PHS, Romiti F, Liu Q, Zhou Y, Hoveyda AH, Ito H. Catalytic Enantioselective Synthesis of Allylic Boronates with a Trisubstituted Alkenyl Fluoride and Conversion to Compounds with a F-Substituted Stereogenic Quaternary Center. Angewandte Chemie (International Ed. in English). PMID 31194906 DOI: 10.1002/Anie.201906283 |
0.6 |
|
| 2017 |
Liu Q, Ni C, Hu J. China's flourishing synthetic organofluorine chemistry: innovations in the new millennium National Science Review. 4: 303-325. DOI: 10.1093/Nsr/Nwx058 |
0.502 |
|
| 2016 |
Liu Q, Shen X, Ni C, Hu J. Stereoselective Carbonyl Olefination with Fluorosulfoximines: Facile Access to Z or E Terminal Monofluoroalkenes. Angewandte Chemie (International Ed. in English). PMID 27879039 DOI: 10.1002/Anie.201610127 |
0.665 |
|
| 2016 |
Shen X, Liu Q, Zhang W, Hu J. Stereoselective Synthesis of (Sulfonimidoyl)cyclopropanes with (R)-PhSO(NTs)CH2Cl and α,β-Unsaturated Weinreb Amides: Tuning the of Selectivity between C-Cl and C-S Bond Cleavage European Journal of Organic Chemistry. 2016: 906-909. DOI: 10.1002/Ejoc.201501611 |
0.682 |
|
| 2016 |
Shen X, Liu Q, Zhang W, Hu J. ChemInform Abstract: Stereoselective Synthesis of (Sulfonimidoyl)cyclopropanes with (R)-PhSO(NTs)CH2Cl and α,β-Unsaturated Weinreb Amides: Tuning the of Selectivity Between C-Cl and C-S Bond Cleavage. Cheminform. 47. DOI: 10.1002/chin.201627075 |
0.549 |
|
| 2014 |
Shen X, Liu Q, Luo T, Hu J. Nucleophilic difluoromethylation of epoxides with PhSO(NTBS)CF₂H by a preorganization strategy. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 6795-800. PMID 24756897 DOI: 10.1002/Chem.201402506 |
0.651 |
|
| 2014 |
Shen X, Liu Q, Ni C, Hu J. Cover Picture: Nucleophilic Difluoro(phenylsulfonimidoyl)methylation of Unactivated Alkyl Bromides with PhSO(NTBS)CF2H: Facile Entry intogem-Difluoroalkenes (Chin. J. Chem. 8/2014) Chinese Journal of Chemistry. 32: 657-657. DOI: 10.1002/Cjoc.201490017 |
0.614 |
|
| 2014 |
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 Chinese Journal of Chemistry. 32: 703-708. DOI: 10.1002/Cjoc.201400403 |
0.669 |
|
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