| Year |
Citation |
Score |
| 2024 |
Lan S, Huang H, Liu W, Xu C, Lei X, Dong W, Liu J, Yang S, Cotman AE, Zhang Q, Fang X. Asymmetric Transfer Hydrogenation of Cyclobutenediones. Journal of the American Chemical Society. PMID 38326715 DOI: 10.1021/jacs.3c14239 |
0.346 |
|
| 2023 |
Dong W, Zhao Z, Gu CZ, Liu JG, Yang S, Fang X. Copper-Catalyzed Umpolung Reactivity of Propargylic Carbonates in the Presence of Diboronates: One Stone Four Birds. Journal of the American Chemical Society. PMID 38019885 DOI: 10.1021/jacs.3c09155 |
0.333 |
|
| 2023 |
Xu C, Zhang H, Lan S, Liu J, Yang S, Zhang Q, Fang X. Copper-Catalysed Rearrangement of Cyclic Ethynylethylene Carbonates: Synthetic Applications and Mechanistic Studies. Angewandte Chemie (International Ed. in English). PMID 36759324 DOI: 10.1002/anie.202219064 |
0.469 |
|
| 2022 |
Chen T, Liu W, Gu W, Niu S, Lan S, Zhao Z, Gong F, Liu J, Yang S, Cotman AE, Song J, Fang X. Dynamic Kinetic Resolution of β-Substituted α-Diketones via Asymmetric Transfer Hydrogenation. Journal of the American Chemical Society. PMID 36563320 DOI: 10.1021/jacs.2c11149 |
0.311 |
|
| 2022 |
Chen T, Gong F, Nagaraju S, Liu J, Yang S, Chen X, Fang X. Oxa-Nazarov Cyclization-Michael Addition Sequence for the Rapid Construction of Dihydrofuranones. Organic Letters. 24: 8837-8842. PMID 36417711 DOI: 10.1021/acs.orglett.2c03601 |
0.713 |
|
| 2021 |
Chen Z, Kong X, Niu S, Yang S, Liu J, Chen B, Luo B, Zhou C, Ding C, Fang X. N-Heterocyclic Carbene-Catalyzed Asymmetric Synthesis of Cyclopentenones. Organic Letters. PMID 33844550 DOI: 10.1021/acs.orglett.1c00870 |
0.439 |
|
| 2020 |
Liu W, Niu S, Zhao Z, Yang S, Liu J, Li Y, Fang X. Divergent Synthesis of Bicyclo[3.2.1]octenes and Cyclohexenes via Catalytic Annulations of Nazarov Reagent and Vinyl 1,2-Diketones. Organic Letters. PMID 32909760 DOI: 10.1021/Acs.Orglett.0C02763 |
0.484 |
|
| 2020 |
Liu R, Yang S, Chen Z, Kong X, Ding H, Fang X. Lewis-Acid-Catalyzed Asymmetric Alkynylation of Alkynyl 1,2-Diketones: Controllable Formation of 3(2)-Furanones and α-Hydroxy Ketones. Organic Letters. PMID 32822188 DOI: 10.1021/Acs.Orglett.0C02505 |
0.516 |
|
| 2020 |
Sun D, Yang S, Fang X. Asymmetric catalytic construction of fully substituted carbon stereocenters using acyclic α-branched β-ketocarbonyls: the “Methyl Rule” widely exists Organic Chemistry Frontiers. 7: 3557-3577. DOI: 10.1039/d0qo00673d |
0.307 |
|
| 2020 |
Liu J, Vasamsetty L, Anwar M, Yang S, Xu W, Liu J, Nagaraju S, Fang X. Organocatalyzed Kinetic Resolution of α-Functionalized Ketones: The Malonate Unit Leads the Way Acs Catalysis. 10: 2882-2893. DOI: 10.1021/Acscatal.9B05608 |
0.417 |
|
| 2019 |
Nagaraju S, Liu S, Liu J, Yang S, Liu R, Chen Z, Paplal B, Fang X. Regioselectivity-Switchable Catalytic Annulations of Alkynyl α-Diketones and α-Cyanoketones. Organic Letters. PMID 31794234 DOI: 10.1021/Acs.Orglett.9B04040 |
0.437 |
|
| 2019 |
Zhao Z, Bagdi PR, Yang S, Liu J, Xu W, Fang X. Stereodivergent Access to Enantioenriched Epoxy Alcohols with Three Stereogenic Centers via Ruthenium-Catalyzed Transfer Hydrogenation. Organic Letters. PMID 31264880 DOI: 10.1021/Acs.Orglett.9B01789 |
0.448 |
|
| 2019 |
Li X, Kong X, Yang S, Meng M, Zhan X, Zeng M, Fang X. Bifunctional Thiourea-Catalyzed Asymmetric Inverse-Electron-Demand Diels-Alder Reaction of Allyl Ketones and Vinyl 1,2-Diketones via Dienolate Intermediate. Organic Letters. PMID 30865466 DOI: 10.1021/Acs.Orglett.9B00035 |
0.58 |
|
| 2019 |
Zehra ST, Zhang G, Yang S, Fang X. Kinetic resolution of β-ketoesters with quaternary stereocenters via a carbene-catalyzed benzoin reaction. Organic & Biomolecular Chemistry. PMID 30720037 DOI: 10.1039/C8Ob02468E |
0.491 |
|
| 2019 |
Xu W, Li Y, Liu R, Yang S, Liu J, Fang X. Kinetic resolution of 2,2-disubstituted-1,3-diketones via carbene catalysis Organic Chemistry Frontiers. 6: 290-298. DOI: 10.1039/C8Qo01137K |
0.428 |
|
| 2019 |
Anwar M, Yang S, Xu W, Liu J, Perveen S, Kong X, Zehra ST, Fang X. Carbene-catalyzed asymmetric Friedel–Crafts alkylation-annulation sequence and rapid synthesis of indole-fused polycyclic alkaloids Communications Chemistry. 2. DOI: 10.1038/s42004-019-0188-2 |
0.347 |
|
| 2019 |
Zhao Z, Yang S, Lan S, Liu J, Liu S, Fang X. Asymmetric Synthesis of Dihydronaphthalene‐1,4‐Diones via Carbene‐Catalyzed Stereodivergent Reaction Advanced Synthesis & Catalysis. 361: 3943-3949. DOI: 10.1002/Adsc.201900506 |
0.566 |
|
| 2018 |
Fang X, Vasamsetty L, Yang S, Meng M, Reddy PS, Kong X, Xu W. Divergent Dynamic Kinetic Resolution of Racemic Mixture of Four Stereoisomers via N-Heterocyclic Carbene Organocatalysis. Chemistry, An Asian Journal. PMID 30303309 DOI: 10.1002/Asia.201801361 |
0.497 |
|
| 2018 |
Kong X, Yang S, Yu F, Vasamsetty L, Liu J, Liu S, Liu X, Fang X. Cyclopentadienone Formation from β,γ-Unsaturated Cyclopentenones and Its Application in Diels-Alder Reactions. The Journal of Organic Chemistry. PMID 29975528 DOI: 10.1021/Acs.Joc.8B01150 |
0.511 |
|
| 2018 |
Kong X, Song J, Liu J, Meng M, Yang S, Zeng M, Zhan X, Li C, Fang X. Brønsted base-catalyzed annulation of allyl ketones and alkynyl 1,2-diketones. Chemical Communications (Cambridge, England). PMID 29629452 DOI: 10.1039/C8Cc01020J |
0.544 |
|
| 2017 |
Liu J, Das DK, Zhang G, Yang S, Zhang H, Fang X. N-Heterocyclic Carbene-Catalyzed Umpolung of β,γ-Unsaturated 1,2-Diketones. Organic Letters. PMID 29266953 DOI: 10.1021/Acs.Orglett.7B03358 |
0.509 |
|
| 2017 |
Zhang G, Xu W, Liu J, Das DK, Yang S, Perveen S, Zhang H, Li X, Fang X. Enantioselective intermolecular all-carbon [4+2] annulation via N-heterocyclic carbene organocatalysis. Chemical Communications (Cambridge, England). PMID 29188838 DOI: 10.1039/C7Cc08680F |
0.554 |
|
| 2017 |
Perveen S, Zhao Z, Zhang G, Liu J, Anwar M, Fang X. Enantioselective Synthesis of 1,2-Dihydronaphthalenes via Oxidative N-Heterocyclic Carbene Catalysis. Organic Letters. PMID 28485600 DOI: 10.1021/Acs.Orglett.7B00555 |
0.526 |
|
| 2017 |
Kong X, Zhang G, Yang S, Liu X, Fang X. N‐Heterocyclic Carbene‐Catalyzed Umpolung of Alkynyl 1,2‐Diketones Advanced Synthesis & Catalysis. 359: 2729-2734. DOI: 10.1002/Adsc.201700700 |
0.549 |
|
| 2016 |
Wang ZA, Zeng Y, Kurra Y, Wang X, Tharp JM, Vatansever EC, Hsu WW, Dai S, Fang X, Liu WR. A Genetically Encoded Allysine for the Synthesis of Proteins with Site-Specific Lysine Dimethylation. Angewandte Chemie (International Ed. in English). PMID 27910233 DOI: 10.1002/Anie.201609452 |
0.315 |
|
| 2016 |
Wen G, Su Y, Zhang G, Lin Q, Zhu Y, Zhang Q, Fang X. Stereodivergent Synthesis of Chromanones and Flavanones via Intramolecular Benzoin Reaction. Organic Letters. PMID 27490010 DOI: 10.1021/Acs.Orglett.6B01767 |
0.588 |
|
| 2016 |
Zhang G, Yang S, Zhang X, Lin Q, Das DK, Liu J, Fang X. Dynamic Kinetic Resolution Enabled by Intramolecular Benzoin Reaction: Synthetic Applications and Mechanistic Insights. Journal of the American Chemical Society. PMID 27270409 DOI: 10.1021/Jacs.6B02929 |
0.595 |
|
| 2016 |
Lin Q, Li Y, Das DK, Zhang G, Zhao Z, Yang S, Fang X. N-Heterocyclic carbene-catalyzed desymmetrization of functionalized 1,4-dienes via Stetter Reaction. Chemical Communications (Cambridge, England). PMID 27100939 DOI: 10.1039/C6Cc01011C |
0.636 |
|
| 2016 |
Li Y, Yang S, Wen G, Lin Q, Zhang G, Qiu L, Zhang X, Du G, Fang X. Asymmetric Desymmetrization of 1,3-Diketones via Intramolecular Benzoin Reaction. The Journal of Organic Chemistry. PMID 26965068 DOI: 10.1021/Acs.Joc.5B02829 |
0.631 |
|
| 2016 |
Song L, Fang X, Wang Z, Liu K, Li C. On the Stereoselectivity of 6-Exo Cyclization of alpha-Carbamoyl Radicals. The Journal of Organic Chemistry. PMID 26926497 DOI: 10.1021/Acs.Joc.6B00008 |
0.702 |
|
| 2016 |
Zhang G, Yang S, Zhang X, Lin Q, Das DK, Liu J, Fang X. ChemInform Abstract: Dynamic Kinetic Resolution Enabled by Intramolecular Benzoin Reaction: Synthetic Applications and Mechanistic Insights. Cheminform. 47. DOI: 10.1002/CHIN.201650077 |
0.38 |
|
| 2016 |
Lin Q, Li Y, Das DK, Zhang G, Zhao Z, Yang S, Fang X. ChemInform Abstract: N-Heterocyclic Carbene-Catalyzed Desymmetrization of Functionalized 1,4-Dienes via Stetter Reaction. Cheminform. 47. DOI: 10.1002/CHIN.201638108 |
0.531 |
|
| 2016 |
Li Y, Yang S, Wen G, Lin Q, Zhang G, Qiu L, Zhang X, Du G, Fang X. ChemInform Abstract: Asymmetric Desymmetrization of 1,3-Diketones via Intramolecular Benzoin Reaction. Cheminform. 47. DOI: 10.1002/CHIN.201633037 |
0.496 |
|
| 2016 |
Song L, Fang X, Wang Z, Liu K, Li C. ChemInform Abstract: Stereoselectivity of 6-Exo Cyclization of α-Carbamoyl Radicals. Cheminform. 47. DOI: 10.1002/CHIN.201631179 |
0.306 |
|
| 2013 |
Sun H, Fang X, Chi YR, Li G. Theoretical study of N-heterocyclic carbenes-catalyzed cascade annulation of benzodienones and enals. Chirality. 25: 521-8. PMID 23798330 DOI: 10.1002/Chir.22157 |
0.7 |
|
| 2013 |
Lee YJ, Wu B, Raymond JE, Zeng Y, Fang X, Wooley KL, Liu WR. A genetically encoded acrylamide functionality. Acs Chemical Biology. 8: 1664-70. PMID 23735044 DOI: 10.1021/Cb400267M |
0.469 |
|
| 2013 |
Chen X, Fang X, Chi YR. cis-Enals in N-heterocyclic carbene-catalyzed reactions: distinct stereoselectivity and reactivity Chemical Science. 4: 2613. DOI: 10.1039/C3Sc50666E |
0.739 |
|
| 2013 |
Chen X, Fang X, Chi YR. ChemInform Abstract: cis-Enals in N-Heterocyclic Carbene-Catalyzed Reactions: Distinct Stereoselectivity and Reactivity. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201345044 |
0.762 |
|
| 2011 |
Fang X, Chen X, Lv H, Chi YR. Enantioselective Stetter reactions of enals and modified chalcones catalyzed by N-heterocyclic carbenes. Angewandte Chemie (International Ed. in English). 50: 11782-5. PMID 21990276 DOI: 10.1002/Anie.201105812 |
0.776 |
|
| 2011 |
Lv H, Mo J, Fang X, Chi YR. Formal Diels-Alder reactions of chalcones and formylcyclopropanes catalyzed by chiral N-heterocyclic carbenes. Organic Letters. 13: 5366-9. PMID 21877756 DOI: 10.1021/Ol202250S |
0.724 |
|
| 2011 |
Fang X, Chen X, Chi YR. Enantioselective Diels-Alder reactions of enals and alkylidene diketones catalyzed by N-heterocyclic carbenes. Organic Letters. 13: 4708-11. PMID 21809839 DOI: 10.1021/Ol201917U |
0.784 |
|
| 2011 |
Fang X, Jiang K, Xing C, Hao L, Chi YR. A highly regio- and stereoselective cascade annulation of enals and benzodi(enone)s catalyzed by N-heterocyclic carbenes. Angewandte Chemie (International Ed. in English). 50: 1910-3. PMID 21328668 DOI: 10.1002/Anie.201007144 |
0.652 |
|
| 2010 |
Fang X, Liu K, Li C. Efficient regio- and stereoselective formation of azocan-2-ones via 8-endo cyclization of alpha-carbamoyl radicals. Journal of the American Chemical Society. 132: 2274-83. PMID 20121130 DOI: 10.1021/Ja9082649 |
0.689 |
|
| 2009 |
Fang X, Xu H, Jiang H, Liu Y, Fu Y, Wu Y. A study on the reactions of NADH models with electron-deficient alkenes. A probe for the extreme of concerted electron-hydrogen atom transfer mechanism Tetrahedron Letters. 50: 312-315. DOI: 10.1016/J.Tetlet.2008.10.143 |
0.681 |
|
| 2007 |
Fang X, Liu YC, Li C. 9-phenyl-10-methylacridinium: a highly efficient and reusable organocatalyst for mild aromatization of 1,4-dihydropyridines by molecular oxygen. The Journal of Organic Chemistry. 72: 8608-10. PMID 17918902 DOI: 10.1021/Jo701796N |
0.686 |
|
| 2007 |
Li C, Pan Y, Lu H, Fang Y, Fang X, Chen L, Qian J, Wang J. Synthesis of Pyrroles via Copper-Catalyzed Coupling of Amines with Bromoenones Synthesis. 2007: 1242-1246. DOI: 10.1055/S-2007-965980 |
0.72 |
|
| 2006 |
Fang X, Liu Y, Wang G, Ke Y. A novel coenzyme NADH model 1-benzyl-1,4-dihydronicotinamide-mediated reaction: a single intermediate serves two mechanisms Research On Chemical Intermediates. 32: 603-611. DOI: 10.1163/156856706778400316 |
0.496 |
|
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