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Wangqing Kong, Ph.D - Publications

Affiliations: 
2002-2006 China University of Geosciences (Wu Han) 
 2006-2011 Zhejiang University, Hangzhou Shi, Zhejiang Sheng, China 
 2011-2014 Universität Zürich, Zürich, ZH, Switzerland 
 2014-2017 École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland 
 2017- Wuhan University, Wuhan Shi, Hubei Sheng, China 
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Year Citation  Score
2024 Liu W, Li W, Xu W, Wang M, Kong W. Nickel-catalyzed switchable arylative/endo-cyclization of 1,6-enynes. Nature Communications. 15: 2914. PMID 38575585 DOI: 10.1038/s41467-024-47200-z  0.454
2024 Liu W, Xing Y, Yan D, Kong W, Shen K. Nickel-catalyzed electrophiles-controlled enantioselective reductive arylative cyclization and enantiospecific reductive alkylative cyclization of 1,6-enynes. Nature Communications. 15: 1787. PMID 38413585 DOI: 10.1038/s41467-024-45617-0  0.495
2023 Pan Q, Ping Y, Kong W. Nickel-Catalyzed Ligand-Controlled Selective Reductive Cyclization/Cross-Couplings. Accounts of Chemical Research. PMID 36688822 DOI: 10.1021/acs.accounts.2c00771  0.404
2022 Liu W, Ke Y, Liu C, Kong W. Direct acylation and alkynylation of hydrocarbons synergistic decatungstate photo-HAT/nickel catalysis. Chemical Communications (Cambridge, England). PMID 36196965 DOI: 10.1039/d2cc04408k  0.344
2022 Ding Z, Kong W. Synthesis of Carbonyl-Containing Oxindoles via Ni-Catalyzed Reductive Aryl-Acylation and Aryl-Esterification of Alkenes. Molecules (Basel, Switzerland). 27. PMID 36144635 DOI: 10.3390/molecules27185899  0.458
2022 Wang K, Chen J, Liu W, Kong W. Nickel-Catalyzed Defluorinative Asymmetric Cyclization of Fluoroalkyl-Substituted 1,6-Enynes for the Synthesis of Seletracetam. Angewandte Chemie (International Ed. in English). PMID 36138513 DOI: 10.1002/anie.202212664  0.412
2022 Ping Y, Pan Q, Guo Y, Liu Y, Li X, Wang M, Kong W. Switchable 1,2-Rearrangement Enables Expedient Synthesis of Structurally Diverse Fluorine-Containing Scaffolds. Journal of the American Chemical Society. PMID 35603358 DOI: 10.1021/jacs.2c02487  0.307
2022 Ping Y, Li X, Pan Q, Kong W. Ni-Catalyzed Divergent Synthesis of 2-Benzazepine Derivatives via Tunable Cyclization and 1,4-Acyl Transfer Triggered by Amide N-C Bond Cleavage. Angewandte Chemie (International Ed. in English). PMID 35385598 DOI: 10.1002/anie.202201574  0.393
2021 Chen H, Zhou Z, Kong W. Allylic alcohol synthesis by Ni-catalyzed direct and selective coupling of alkynes and methanol. Chemical Science. 12: 9372-9378. PMID 34349909 DOI: 10.1039/d1sc02625a  0.437
2021 Li H, Chen J, Dong J, Kong W. Ni-Catalyzed Reductive Arylcyanation of Alkenes. Organic Letters. PMID 34342232 DOI: 10.1021/acs.orglett.1c02270  0.457
2021 Pan Q, Ping Y, Wang Y, Guo Y, Kong W. Ni-Catalyzed Ligand-Controlled Regiodivergent Reductive Dicarbofunctionalization of Alkenes. Journal of the American Chemical Society. PMID 34162201 DOI: 10.1021/jacs.1c03827  0.395
2021 Chen XW, Yue JP, Wang K, Gui YY, Niu YN, Liu J, Ran CK, Kong W, Zhou WJ, Yu DG. Nickel-Catalyzed Asymmetric Reductive Carbo-Carboxylation of Alkenes with CO2. Angewandte Chemie (International Ed. in English). PMID 33793030 DOI: 10.1002/anie.202102769  0.476
2020 Zhou Z, Chen J, Chen H, Kong W. Stereoselective synthesis of pentasubstituted 1,3-dienes Ni-catalyzed reductive coupling of unsymmetrical internal alkynes. Chemical Science. 11: 10204-10211. PMID 34094285 DOI: 10.1039/d0sc04173d  0.391
2020 Ding Z, Wang Y, Liu W, Chen Y, Kong W. Diastereo- and Enantioselective Construction of Spirocycles by Nickel-Catalyzed Cascade Borrowing Hydrogen Cyclization. Journal of the American Chemical Society. PMID 33356186 DOI: 10.1021/jacs.0c10055  0.404
2020 Chen Y, Ding Z, Wang Y, Liu W, Kong W. Synthesis of Indanones and Spiroindanones by Diastereoselective Annulation Based on a Hydrogen Autotransfer Strategy. Angewandte Chemie (International Ed. in English). PMID 33205565 DOI: 10.1002/anie.202013792  0.458
2020 Zhou Z, Liu W, Kong W. Ni-Catalyzed Reductive Antiarylative Cyclization of Alkynones. Organic Letters. PMID 32847361 DOI: 10.1021/Acs.Orglett.0C02534  0.455
2020 Chen J, Wang Y, Ding Z, Kong W. Synthesis of bridged tricyclo[5.2.1.0]decanes via nickel-catalyzed asymmetric domino cyclization of enynones. Nature Communications. 11: 1882. PMID 32312990 DOI: 10.1038/s41467-020-15837-1  0.475
2020 Ping Y, Kong W. Ni-Catalyzed Reductive Difunctionalization of Alkenes Synthesis. 52: 979-992. DOI: 10.1055/S-0039-1690807  0.603
2020 Zhou Z, Xu S, Zhang J, Kong W. Nickel-Catalyzed Enantioselective Electroreductive Cross-Couplings Organic Chemistry Frontiers. DOI: 10.1039/D0Qo00901F  0.373
2019 Ju B, Chen S, Kong W. Pd-Catalyzed Enantioselective Double Heck Reaction. Organic Letters. PMID 31763841 DOI: 10.1021/Acs.Orglett.9B03517  0.535
2019 Ju B, Chen S, Kong W. Enantioselective palladium-catalyzed diarylation of unactivated alkenes. Chemical Communications (Cambridge, England). PMID 31713555 DOI: 10.1039/C9Cc07036B  0.549
2019 Xu S, Wang K, Kong W. Ni-Catalyzed Reductive Arylacylation of Alkenes toward Carbonyl-Containing Oxindoles. Organic Letters. PMID 31479280 DOI: 10.1021/Acs.Orglett.9B02788  0.545
2019 Wang K, Kong W. Enantioselective Reductive Diarylation of Alkenes by Ni-Catalyzed Domino Heck Cyclization/Cross Coupling Synlett. 30: 1008-1014. DOI: 10.1055/S-0037-1612214  0.538
2019 Li Y, Ding Z, Lei A, Kong W. Ni-Catalyzed enantioselective reductive aryl-alkenylation of alkenes: application to the synthesis of (+)-physovenine and (+)-physostigmine Organic Chemistry Frontiers. 6: 3305-3309. DOI: 10.1039/C9Qo00744J  0.514
2019 Ma T, Chen Y, Li Y, Ping Y, Kong W. Nickel-Catalyzed Enantioselective Reductive Aryl Fluoroalkenylation of Alkenes Acs Catalysis. 9: 9127-9133. DOI: 10.1021/Acscatal.9B03172  0.573
2019 Ping Y, Wang K, Pan Q, Ding Z, Zhou Z, Guo Y, Kong W. Ni-Catalyzed Regio- and Enantioselective Domino Reductive Cyclization: One-Pot Synthesis of 2,3-Fused Cyclopentannulated Indolines Acs Catalysis. 9: 7335-7342. DOI: 10.1021/Acscatal.9B02081  0.577
2018 Wang K, Ding Z, Zhou Z, Kong W. Ni-Catalyzed Enantioselective Reductive Diarylation of Activated Alkenes by Domino Cyclization/Cross-Coupling. Journal of the American Chemical Society. PMID 30234979 DOI: 10.1021/Jacs.8B08190  0.547
2018 Ping Y, Li Y, Zhu J, Kong W. Construction of Quaternary Stereocenters by Palladium-Catalyzed Carbopalladation-Initiated Cascade Reactions. Angewandte Chemie (International Ed. in English). PMID 29959826 DOI: 10.1002/Anie.201806088  0.575
2018 Li Y, Wang K, Ping Y, Wang Y, Kong W. Nickel-Catalyzed Domino Heck Cyclization/Suzuki Coupling for the Synthesis of 3,3-Disubstituted Oxindoles. Organic Letters. PMID 29373029 DOI: 10.1021/Acs.Orglett.7B03713  0.61
2018 Wang K, Kong W. Cover Picture: Recent Advances in Transition Metal‐Catalyzed Asymmetric Radical Reactions (Chin. J. Chem. 3/2018) Chinese Journal of Chemistry. 36: 173-173. DOI: 10.1002/Cjoc.201880031  0.435
2018 Wang K, Kong W. Recent Advances in Transition Metal‐Catalyzed Asymmetric Radical Reactions Chinese Journal of Chemistry. 36: 247-256. DOI: 10.1002/Cjoc.201700745  0.45
2017 Kong W, Wang Q, Zhu J. Water as a Hydride Source in Palladium-Catalyzed Enantioselective Reductive Heck Reactions. Angewandte Chemie (International Ed. in English). PMID 28272769 DOI: 10.1002/Anie.201700195  0.601
2016 Kong W, Wang Q, Zhu J. Synthesis of Diversely Functionalized Oxindoles Enabled by Migratory Insertion of Isocyanide to a Transient σ-Alkylpalladium(II) Complex. Angewandte Chemie (International Ed. in English). PMID 27356093 DOI: 10.1002/Anie.201603950  0.522
2015 Kong W, Wang Q, Zhu J. Palladium-Catalyzed Enantioselective Domino Heck/Intermolecular C-H Bond Functionalization: Development and Application to the Synthesis of (+)-Esermethole. Journal of the American Chemical Society. PMID 26681502 DOI: 10.1021/Jacs.5B11625  0.619
2015 Fuentes N, Kong W, Fernández-Sánchez L, Merino E, Nevado C. Correction to "Cyclization Cascades via N-Amidyl Radicals toward Highly Functionalized Heterocyclic Scaffolds". Journal of the American Chemical Society. 137: 5852. PMID 25909145 DOI: 10.1021/Jacs.5B03070  0.607
2015 Kong W, Fuentes N, García-Domínguez A, Merino E, Nevado C. Stereoselective synthesis of highly functionalized indanes and dibenzocycloheptadienes through complex radical cascade reactions. Angewandte Chemie (International Ed. in English). 54: 2487-91. PMID 25597296 DOI: 10.1002/Anie.201409659  0.704
2015 Fuentes N, Kong W, Fernández-Sánchez L, Merino E, Nevado C. Cyclization cascades via N-amidyl radicals toward highly functionalized heterocyclic scaffolds. Journal of the American Chemical Society. 137: 964-73. PMID 25561161 DOI: 10.1021/Ja5115858  0.654
2014 Kong W, Merino E, Nevado C. Divergent reaction mechanisms in the aminofluorination of alkenes. Chimia. 68: 430-5. PMID 25198754 DOI: 10.2533/Chimia.2014.430  0.676
2014 Kong W, Merino E, Nevado C. Arylphosphonylation and arylazidation of activated alkenes. Angewandte Chemie (International Ed. in English). 53: 5078-82. PMID 24692217 DOI: 10.1002/Anie.201311241  0.655
2014 Qiu Y, Ma D, Kong W, Fu C, Ma S. Regiocontrolled 1,2-migration in cyclization of 1-(indol-2-yl)-3-alkyn-1-ols: (Ph3P)Au+vs. PtCl4 Org. Chem. Front.. 1: 62-67. DOI: 10.1039/C3Qo00006K  0.642
2013 Kong W, Casimiro M, Fuentes N, Merino E, Nevado C. Metal-free aryltrifluoromethylation of activated alkenes. Angewandte Chemie (International Ed. in English). 52: 13086-90. PMID 24174281 DOI: 10.1002/Anie.201307377  0.563
2013 Kong W, Casimiro M, Merino E, Nevado C. Copper-catalyzed one-Pot trifluoromethylation/aryl migration/ desulfonylation and C(sp2)-N bond formation of conjugated tosyl amides Journal of the American Chemical Society. 135: 14480-14483. PMID 24047140 DOI: 10.1021/Ja403954G  0.69
2013 Kong W, Feige P, De Haro T, Nevado C. Regio- and enantioselective aminofluorination of alkenes Angewandte Chemie - International Edition. 52: 2469-2473. PMID 23362120 DOI: 10.1002/Anie.201208471  0.671
2013 Snieckus V, Rocke BN, Kong W, Feige P, Haro Td, Nevado C. Piperidines and Azepines via Asymmetric Aminofluorination of Olefins Synfacts. 9: 371-371. DOI: 10.1055/S-0032-1318450  0.497
2013 Qiu Y, Kong W, Fu C, Ma S. ChemInform Abstract: Carbazoles via AuCl3-Catalyzed Cyclization of 1-(Indol-2-yl)-3-alkyn-1-ols. Cheminform. 44: no-no. DOI: 10.1002/chin.201319117  0.618
2013 Kong W, Qiu Y, Zhang X, Fu C, Ma S. ChemInform Abstract: Exclusive 1,2-Aryl Shift in Platinum(II) Chloride Catalyzed Cyclization of 1-(Indol-2-yl)-2,3-allenols. Cheminform. 44: no-no. DOI: 10.1002/chin.201310130  0.502
2012 Qiu Y, Kong W, Fu C, Ma S. Carbazoles via AuCl3-catalyzed cyclization of 1-(indol-2-yl)-3-alkyn-1-ols. Organic Letters. 14: 6198-201. PMID 23228044 DOI: 10.1021/Ol3029498  0.648
2012 Kong W, Fu C, Ma S. Efficient synthesis of carbazoles via PtCl2-catalyzed RT cyclization of 1-(indol-2-yl)-2,3-allenols: scope and mechanism. Organic & Biomolecular Chemistry. 10: 2164-73. PMID 22299129 DOI: 10.1039/C1Ob06474F  0.67
2012 Kong W, Fu C, Ma S. ChemInform Abstract: Efficient Synthesis of Carbazoles via PtCl2-Catalyzed RT Cyclization of 1-(Indol-2-yl)-2,3-allenols: Scope and Mechanism. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201231119  0.443
2012 Kong W, Qiu Y, Zhang X, Fu C, Ma S. Exclusive 1,2-Aryl Shift in Platinum(II) Chloride-Catalyzed Cyclization of 1-(Indol-2-yl)-2,3-allenols Advanced Synthesis & Catalysis. 354: 2339-2347. DOI: 10.1002/Adsc.201100935  0.609
2011 Kong W, Fu C, Ma S. General Au-catalyzed benzannulation towards naturally occurring carbazole alkaloids from methoxypropadiene. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 13134-7. PMID 21990042 DOI: 10.1002/Chem.201102251  0.509
2011 Kong W, Guo B, Fu C, Ma S. An Efficient Approach to 2-Bromoalken-3-ols by Regioselective Bromohydroxylation Reaction of Simple Allenes with NBS European Journal of Organic Chemistry. 2011: 2278-2285. DOI: 10.1002/Ejoc.201001676  0.611
2011 Kong W, Guo B, Fu C, Ma S. ChemInform Abstract: An Efficient Approach to 2-Bromoalken-3-ols by Regioselective Bromohydroxylation Reaction of Simple Allenes with NBS. Cheminform. 42: no-no. DOI: 10.1002/chin.201135045  0.56
2011 Kong W, Fu C, Ma S. ChemInform Abstract: An Efficient Synthesis of Polysubstituted Naphthalene Derivatives by Gold-Catalyzed Cyclization of 1-Arylalka-2,3-dienyl Acetates. Cheminform. 42: no-no. DOI: 10.1002/chin.201114103  0.569
2010 Kong W, Fu C, Ma S. An Efficient Synthesis of Polysubstituted Naphthalene Derivatives by Gold-Catalyzed Cyclization of 1-Arylalka-2,3-dienyl Acetates (Eur. J. Org. Chem. 34/2010) European Journal of Organic Chemistry. 2010: n/a-n/a. DOI: 10.1002/Ejoc.201090094  0.586
2010 Kong W, Fu C, Ma S. An Efficient Synthesis of Polysubstituted Naphthalene Derivatives by Gold-Catalyzed Cyclization of 1-Arylalka-2,3-dienyl Acetates European Journal of Organic Chemistry. 2010: 6545-6555. DOI: 10.1002/Ejoc.201001112  0.648
2010 Li J, Kong W, Yu Y, Fu C, Ma S. ChemInform Abstract: Electrophilic Reaction of Tertiary 2,3-Allenols with NBS in H2O or Aqueous MeCN: An Efficient Selective Synthesis of 2-Bromoallylic Ketones; 1,2-Allenyl Ketones, or 3-Bromo-2,5-dihydrofurans. Cheminform. 41. DOI: 10.1002/chin.201012064  0.61
2009 Li J, Kong W, Yu Y, Fu C, Ma S. Studies on electrophilic reaction of tertiary 2,3-allenols with NBS in H2O or aqueous MeCN: an efficient selective synthesis of 2-bromoallylic ketones, 1,2-allenyl ketones, or 3-bromo-2,5-dihydrofurans. The Journal of Organic Chemistry. 74: 8733-8. PMID 19873989 DOI: 10.1021/Jo9018717  0.656
2009 Kong W, Fu C, Ma S. An efficient synthesis of carbazoles from PtCl(2)-catalyzed cyclization of 1-(indol-2-yl)-2,3-allenols. Chemical Communications (Cambridge, England). 4572-4. PMID 19617987 DOI: 10.1039/B909649C  0.531
2009 Li J, Kong W, Fu C, Ma S. An efficient CuCN-catalyzed synthesis of optically active 2,3-allenols from optically active 1-substituted 4-chloro-2-butyn-1-ols. The Journal of Organic Chemistry. 74: 5104-6. PMID 19476327 DOI: 10.1021/Jo900710E  0.492
2009 Kong W, Cui J, Yu Y, Chen G, Fu C, Ma S. PtCl4-catalyzed cyclization reaction of beta-allenols in the presence of indoles. Organic Letters. 11: 1213-6. PMID 19215143 DOI: 10.1021/Ol802838V  0.581
2009 Kong W, Cui J, Yu Y, Chen G, Fu C, Ma S. ChemInform Abstract: PtCl4-Catalyzed Cyclization Reaction of β-Allenols in the Presence of Indoles. Cheminform. 40. DOI: 10.1002/chin.200931109  0.55
2009 Kong W, Fu C, Ma S. ChemInform Abstract: Indium- and Zinc-Mediated Barbier-Type Addition Reaction of 2,3-Allenals with Allyl Bromide: An Efficient Synthesis of 1,5,6-Alkatrien-4-ols. Cheminform. 40. DOI: 10.1002/chin.200917054  0.6
2008 Jiang X, Kong W, Chen J, Ma S. Intermolecular sequential [4 + 2]-cycloaddition-aromatization reaction of aryl-substituted allenes with DMAD affording phenanthrene and naphthalene derivatives. Organic & Biomolecular Chemistry. 6: 3606-10. PMID 19082163 DOI: 10.1039/B808767A  0.724
2008 Kong W, Fu C, Ma S. Indium and zinc-mediated Barbier-type addition reaction of 2,3-allenals with allyl bromide: an efficient synthesis of 1,5,6-alkatrien-4-ols. Organic & Biomolecular Chemistry. 6: 4587-92. PMID 19039368 DOI: 10.1039/B812869C  0.648
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