Year |
Citation |
Score |
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 |
0.47 |
|
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 |
0.637 |
|
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 |
0.701 |
|
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 |
0.725 |
|
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 |
0.654 |
|
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 |
0.69 |
|
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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