| Year |
Citation |
Score |
| 2024 |
Li Z, Wang B, Zhang C, Lo WY, Yang L, Sun J. Catalytic Enantioselective Nucleophilic α-Chlorination of Ketones with NaCl. Journal of the American Chemical Society. PMID 38238317 DOI: 10.1021/jacs.3c12826 |
0.412 |
|
| 2024 |
Gao W, Yang Q, Yang H, Yao Y, Bai J, Sun J, Sun S. Visible-Light Photoredox-Catalyzed Intermolecular α-Aminomethyl/Carboxylative Dearomatization of Indoles with CO and α-Aminoalkyl Radical Precursors. Organic Letters. PMID 38179973 DOI: 10.1021/acs.orglett.3c03755 |
0.333 |
|
| 2024 |
Li S, Feng Q, Song L, Zhang X, Wu YD, Sun J. Mild Stereoselective Synthesis of Densely Substituted [3]Dendralenes via Ru-Catalyzed Intermolecular Dimerization of 1,1-Disubstituted Allenes. Journal of the American Chemical Society. PMID 38174923 DOI: 10.1021/jacs.3c11448 |
0.46 |
|
| 2024 |
Su X, Wang Y, Feng Q, Sun J. Heterodifunctionalization of Electron-Rich Alkynes Catalyzed by Generated Silylium Ions. Organic Letters. PMID 38166166 DOI: 10.1021/acs.orglett.3c04208 |
0.379 |
|
| 2024 |
Li Y, Huang J, Han Z, Huang H, Hong B, Sun J. Organocatalytic Enantioselective Nucleophilic Addition of Indole Imine 5-Methides. Organic Letters. PMID 38165742 DOI: 10.1021/acs.orglett.3c04070 |
0.471 |
|
| 2023 |
Han Z, Zhu B, Zang Y, Zhang C, Dong XQ, Huang H, Sun J. Primary activation of -quinone methides by chiral phosphoric acid for enantioselective construction of tetraarylmethanes. Chemical Science. 15: 720-725. PMID 38179542 DOI: 10.1039/d3sc05014a |
0.445 |
|
| 2023 |
Zhu H, Xu L, Zhu B, Liao M, Li J, Han Z, Sun J, Huang H. Copper-Catalyzed Enantioselective Formal [4 + 1] and [3 + 3] Cycloaddition of Ethynylethylene Carbonates. Organic Letters. 25: 9213-9218. PMID 38100085 DOI: 10.1021/acs.orglett.3c03871 |
0.441 |
|
| 2023 |
Li J, Fang M, Liao M, Xie H, Dong XQ, Han Z, Sun J, Huang H. Synthesis of medium-sized heterocycles from oxetanes based on an allylic amination/ring-opening strategy. Chemical Communications (Cambridge, England). PMID 37986611 DOI: 10.1039/d3cc04355j |
0.354 |
|
| 2023 |
Wang J, Yu R, Nian C, Liao M, Han Z, Sun J, Huang H. Metal-Free C(sp)-H Bond Arylation of 3-Methylindole Derivatives via 3-Indole Imine Methides. Organic Letters. PMID 37966338 DOI: 10.1021/acs.orglett.3c03406 |
0.324 |
|
| 2023 |
Zhan H, Chen B, Zhu B, Li X, Han Z, Sun J, Huang H. Construction of 5-methyleneoxazolidine-2,4-diones bearing modifiable halogen groups through a halopalladation strategy. Chemical Communications (Cambridge, England). PMID 37902867 DOI: 10.1039/d3cc04475k |
0.374 |
|
| 2023 |
Han Z, Xue Y, Li X, Hu X, Dong XQ, Sun J, Huang H. Studies on the [4 + 2] cycloaddition and allylic substitution of indole-fused zwitterionic π-allylpalladium. Organic & Biomolecular Chemistry. PMID 37782136 DOI: 10.1039/d3ob01451g |
0.457 |
|
| 2023 |
Yang Q, Bai J, Yang H, Yao Y, Yao Y, Sun J, Sun S. [Cp*IrCl]-Catalyzed Amidocarbonation of Olefins with Sulfoxonium Ylides toward Functionalized Isoindolin-1-ones. Organic Letters. PMID 37751295 DOI: 10.1021/acs.orglett.3c02654 |
0.42 |
|
| 2023 |
Yang Z, Bao Y, Huang J, Han Z, Sun J, Huang H. Tandem Allylic Amination/oxa-Michael Addition of Vinyl Methylene Cyclic Carbonates via Palladium-Organo Relay Catalysis. Organic Letters. 25: 5624-5629. PMID 37486245 DOI: 10.1021/acs.orglett.3c02014 |
0.507 |
|
| 2023 |
Xie H, Chen L, Han Z, Yang Z, Sun J, Huang H. Pd-Catalyzed Ligand-Directed Divergent Cycloaddition of Cyclic 1-Azadienes with Oxo-1,4-dipoles. Organic Letters. PMID 37382587 DOI: 10.1021/acs.orglett.3c01646 |
0.399 |
|
| 2023 |
Liu S, Chan KL, Lin Z, Sun J. Asymmetric Synthesis of Remotely Chiral Naphthols and Naphthylamines via Naphthoquinone Methides. Journal of the American Chemical Society. PMID 37276009 DOI: 10.1021/jacs.3c03557 |
0.52 |
|
| 2023 |
Liu C, Sun J, Li P. Chiral Phosphine Catalyzed Allylic Alkylation of Benzylidene Succinimides with Morita-Baylis-Hillman Carbonates. Molecules (Basel, Switzerland). 28. PMID 36985797 DOI: 10.3390/molecules28062825 |
0.436 |
|
| 2023 |
Tan X, Wang Q, Sun J. Electricity-driven asymmetric bromocyclization enabled by chiral phosphate anion phase-transfer catalysis. Nature Communications. 14: 357. PMID 36690612 DOI: 10.1038/s41467-023-36000-6 |
0.347 |
|
| 2023 |
Wang Y, Li Y, Wang L, Ding S, Song L, Zhang X, Wu YD, Sun J. Ir-Catalyzed Regioselective Dihydroboration of Thioalkynes toward -Diboryl Thioethers. Journal of the American Chemical Society. PMID 36657379 DOI: 10.1021/jacs.2c10881 |
0.517 |
|
| 2023 |
Han Z, Wang W, Zhuang H, Wang J, Wang C, Wang J, Huang H, Sun J. Catalytic Enantioselective Synthesis of 2,3'-Bis(indolyl)methanes Bearing All-Carbon Quaternary Stereocenters via 2-Indole Imine Methides. Organic Letters. PMID 36641768 DOI: 10.1021/acs.orglett.2c04109 |
0.471 |
|
| 2023 |
Zhou Y, Yue X, Jiang F, Sun J, Guo W. Catalytic asymmetric synthesis of α-tertiary aminoketones from sulfoxonium ylides bearing two aryl groups. Chemical Communications (Cambridge, England). PMID 36629287 DOI: 10.1039/d2cc06147c |
0.43 |
|
| 2022 |
Guo W, Zhou Y, Xie H, Yue X, Jiang F, Huang H, Han Z, Sun J. Visible-light-induced organocatalytic enantioselective N-H insertion of α-diazoesters enabled by indirect free carbene capture. Chemical Science. 14: 843-848. PMID 36755716 DOI: 10.1039/d2sc05149d |
0.352 |
|
| 2022 |
Li W, Zhang H, Chen K, Jiang H, Sun J, Zhu S. Palladium-catalyzed intramolecular enantioselective C(sp)-H insertion of donor/donor carbenes. Chemical Science. 13: 12396-12402. PMID 36382271 DOI: 10.1039/d2sc03524c |
0.419 |
|
| 2022 |
Yang Z, Xie H, Tang L, Sun J, Han Z, Huang H. Construction of diverse polycyclic N-heterocycles cascade allylic amination/Diels-Alder reaction. Chemical Communications (Cambridge, England). PMID 36367142 DOI: 10.1039/d2cc05208c |
0.447 |
|
| 2022 |
Guo W, Jiang F, Li S, Sun J. Organocatalytic asymmetric azidation of sulfoxonium ylides: mild synthesis of enantioenriched α-azido ketones bearing a labile tertiary stereocenter. Chemical Science. 13: 11648-11655. PMID 36320381 DOI: 10.1039/d2sc03552a |
0.535 |
|
| 2022 |
Li LX, Min L, Yao TB, Ji SX, Qiao C, Tian PL, Sun J, Li CC. Total Synthesis of Yuzurine-type Alkaloid Daphgraciline. Journal of the American Chemical Society. PMID 36198113 DOI: 10.1021/jacs.2c09548 |
0.416 |
|
| 2022 |
Qian C, Huang T, Sun J, Li P. Catalyst-Controlled Divergent Reactions of 2,3-Disubstituted Indoles with Propargylic Alcohols: Synthesis of 3-Benzo[]azepines and Axially Chiral Tetrasubstituted Allenes. Organic Letters. 24: 6472-6476. PMID 36040372 DOI: 10.1021/acs.orglett.2c02642 |
0.489 |
|
| 2022 |
Sha Y, Bai J, Li M, Gao W, Yang Q, Sun J, Sun S. Base-Promoted 5-- Cyclization of -Alkynylamides or 2-En-4-ynamides with CO toward Fully Substituted Acrylates. Organic Letters. PMID 35921535 DOI: 10.1021/acs.orglett.2c02123 |
0.393 |
|
| 2022 |
Feng Q, Li S, Li Z, Yan Q, Lin X, Song L, Zhang X, Wu YD, Sun J. Ru-Catalyzed Hydroboration of Ynones Leads to a Nontraditional Mode of Reactivity. Journal of the American Chemical Society. PMID 35900878 DOI: 10.1021/jacs.2c06024 |
0.378 |
|
| 2022 |
Yan Q, Duan M, Chen C, Deng Z, Wu M, Yu P, He ML, Zhu G, Houk KN, Sun J. Organocatalytic discrimination of non-directing aryl and heteroaryl groups: enantioselective synthesis of bioactive indole-containing triarylmethanes. Chemical Science. 13: 5767-5773. PMID 35694360 DOI: 10.1039/d2sc00636g |
0.402 |
|
| 2022 |
Han Z, Zang Y, Liu C, Guo W, Huang H, Sun J. Enantioselective synthesis of triarylmethanes organocatalytic transfer hydrogenation of -quinone methides. Chemical Communications (Cambridge, England). PMID 35667384 DOI: 10.1039/d2cc01996e |
0.473 |
|
| 2022 |
Han Z, Zhuang H, Tang L, Zang Y, Guo W, Huang H, Sun J. Catalytic Asymmetric Allylic Substitution/Isomerization with Central Chirality Transposition. Organic Letters. 24: 4246-4251. PMID 35657160 DOI: 10.1021/acs.orglett.2c01559 |
0.485 |
|
| 2022 |
Tan YX, Li S, Song L, Zhang X, Wu YD, Sun J. Ruthenium-Catalyzed Geminal Hydroborative Cyclization of Enynes. Angewandte Chemie (International Ed. in English). PMID 35596681 DOI: 10.1002/anie.202204319 |
0.439 |
|
| 2022 |
Zhang R, Sun M, Yan Q, Lin X, Li X, Fang X, Sung HHY, Williams ID, Sun J. Asymmetric Synthesis of Pyrrolidines via Oxetane Desymmetrization. Organic Letters. 24: 2359-2364. PMID 35322664 DOI: 10.1021/acs.orglett.2c00564 |
0.451 |
|
| 2022 |
Tang M, Cameron L, Poland EM, Yu LJ, Moggach SA, Fuller RO, Huang H, Sun J, Thickett SC, Massi M, Coote ML, Ho CC, Bissember AC. Photoactive Metal Carbonyl Complexes Bearing N-Heterocyclic Carbene Ligands: Synthesis, Characterization, and Viability as Photoredox Catalysts. Inorganic Chemistry. PMID 35025492 DOI: 10.1021/acs.inorgchem.1c02964 |
0.678 |
|
| 2021 |
Zhang T, Zhuang H, Tang L, Han Z, Guo W, Huang H, Sun J. Catalytic Enantioselective Synthesis of 2,3-Dihydrobenzo[]oxepines via Asymmetric Oxetane Opening by Internal Carbon Nucleophiles. Organic Letters. PMID 34914391 DOI: 10.1021/acs.orglett.1c03852 |
0.441 |
|
| 2021 |
Bai J, Li M, Zhou C, Sha Y, Cheng J, Sun J, Sun S. Visible-Light Photoredox-Catalyzed Dicarbofunctionalization of Styrenes with Oxime Esters and CO: Multicomponent Reactions toward Cyanocarboxylic Acids and γ-Keto Acids. Organic Letters. PMID 34851115 DOI: 10.1021/acs.orglett.1c03938 |
0.347 |
|
| 2021 |
Zhang R, Ge S, Sun J. Correction to "SPHENOL, A New Chiral Framework for Asymmetric Synthesis". Journal of the American Chemical Society. PMID 34662110 DOI: 10.1021/jacs.1c10524 |
0.386 |
|
| 2021 |
Li Z, Li Y, Li X, Wu M, He ML, Sun J. Organocatalytic asymmetric formal oxidative coupling for the construction of all-aryl quaternary stereocenters. Chemical Science. 12: 11793-11798. PMID 34659717 DOI: 10.1039/d1sc03324g |
0.408 |
|
| 2021 |
Guo W, Wang M, Han Z, Huang H, Sun J. Organocatalytic asymmetric synthesis of α-amino esters from sulfoxonium ylides. Chemical Science. 12: 11191-11196. PMID 34522316 DOI: 10.1039/d1sc02439f |
0.506 |
|
| 2021 |
Li X, Duan M, Yu P, Houk KN, Sun J. Organocatalytic enantioselective dearomatization of thiophenes by 1,10-conjugate addition of indole imine methides. Nature Communications. 12: 4881. PMID 34385441 DOI: 10.1038/s41467-021-25165-7 |
0.452 |
|
| 2021 |
Zhang R, Ge S, Sun J. SPHENOL, A New Chiral Framework for Asymmetric Synthesis. Journal of the American Chemical Society. PMID 34358424 DOI: 10.1021/jacs.1c05709 |
0.464 |
|
| 2021 |
Liu S, Qian H, Zhang T, Xie H, Han Z, Guo W, Huang H, Sun J. A Mild Intermolecular Synthesis of Cyclopropane-Incorporated Tricyclic Skeleton: Unusual Reactivity of Isobenzopyryliums. Angewandte Chemie (International Ed. in English). PMID 34342934 DOI: 10.1002/anie.202108258 |
0.385 |
|
| 2021 |
Feng Q, Wu A, Zhang X, Song L, Sun J. An unusual formal migrative cycloaddition of aurone-derived azadienes: synthesis of benzofuran-fused nitrogen heterocycles. Chemical Science. 12: 7953-7957. PMID 34168849 DOI: 10.1039/d1sc00941a |
0.348 |
|
| 2021 |
Feng Q, Wu A, Zhang X, Song L, Sun J. An unusual formal migrative cycloaddition of aurone-derived azadienes: synthesis of benzofuran-fused nitrogen heterocycles. Chemical Science. 12: 7953-7957. PMID 34168849 DOI: 10.1039/d1sc00941a |
0.348 |
|
| 2021 |
Zhou C, Li M, Sun J, Cheng J, Sun S. Photoredox-Catalyzed α-Aminomethyl Carboxylation of Styrenes with Sodium Glycinates: Synthesis of γ-Amino Acids and γ-Lactams. Organic Letters. PMID 33783223 DOI: 10.1021/acs.orglett.1c00536 |
0.369 |
|
| 2020 |
Lai Z, Zhang R, Feng Q, Sun J. 3-Aminooxetanes: versatile 1,3-amphoteric molecules for intermolecular annulation reactions. Chemical Science. 11: 9945-9949. PMID 34094256 DOI: 10.1039/d0sc04254d |
0.32 |
|
| 2020 |
Wu A, Qian H, Zhao W, Sun J. Benzannulation of isobenzopyryliums with electron-rich alkynes: a modular access to β-functionalized naphthalenes. Chemical Science. 11: 7957-7962. PMID 34094164 DOI: 10.1039/d0sc02502j |
0.346 |
|
| 2020 |
Huang H, Zhang T, Sun J. Mild C-C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with Soft Carbon Nucleophiles. Angewandte Chemie (International Ed. in English). PMID 33459485 DOI: 10.1002/anie.202013062 |
0.39 |
|
| 2020 |
Sun S, Wang Z, Li S, Zhou C, Song L, Huang H, Sun J. An Organocatalytic Kinetic Resolution of Aziridines by Thiol Nucleophiles. Organic Letters. PMID 33382271 DOI: 10.1021/acs.orglett.0c04074 |
0.805 |
|
| 2020 |
Qian C, Li P, Sun J. Catalytic Enantioselective Synthesis of Spirooxindoles by Oxidative Rearrangement of Indoles. Angewandte Chemie (International Ed. in English). PMID 33283414 DOI: 10.1002/anie.202015175 |
0.44 |
|
| 2020 |
Liu S, Zang Y, Huang H, Sun J. In(OTf)-Catalyzed Synthesis of 2,3-Dihydro-1-benzo[]indoles and 2,3-Dihydrobenzofurans via [3 + 2] Annulation. Organic Letters. PMID 33034458 DOI: 10.1021/acs.orglett.0c02729 |
0.457 |
|
| 2020 |
Qian H, Sun S, Zhao W, Sun J. An efficient [3+2] annulation for the asymmetric synthesis of densely-functionalized pyrrolidinones and γ-butenolides. Chemical Communications (Cambridge, England). PMID 32839794 DOI: 10.1039/D0Cc05188H |
0.531 |
|
| 2020 |
Guo W, Luo Y, Sung HHY, Williams ID, Li P, Sun J. Chiral Phosphoric Acid Catalyzed Enantioselective Synthesis of α-Tertiary Amino Ketones from Sulfonium Ylides. Journal of the American Chemical Society. PMID 32697915 DOI: 10.1021/Jacs.0C07210 |
0.56 |
|
| 2020 |
Feng Q, Wu HN, Li X, Song L, Chung LW, Wu YD, Sun J. Ru-Catalyzed Geminal Hydroboration of Silyl Alkynes via a New gem-Addition Mechanism. Journal of the American Chemical Society. PMID 32668156 DOI: 10.1021/Jacs.0C05334 |
0.485 |
|
| 2020 |
Li X, Sun J. Organocatalytic Enantioselective Synthesis of Chiral Allenes: Remote Asymmetric 1,8-Addition of Indole Imine Methides. Angewandte Chemie (International Ed. in English). PMID 32558012 DOI: 10.1002/Anie.202006137 |
0.581 |
|
| 2020 |
Wang G, Huang H, Guo W, Qian C, Sun J. Unusual Skeletal Reorganization of Oxetanes for the Synthesis of 1,2-Dihydroquinolines. Angewandte Chemie (International Ed. in English). PMID 32219976 DOI: 10.1002/Anie.201916727 |
0.551 |
|
| 2020 |
Wong THM, Li X, Ma D, Sun J. HNTf-Catalyzed Synthesis of Hydrodibenzofurans by an Epoxidation/Semipinacol Rearrangement Cascade. Organic Letters. PMID 32091907 DOI: 10.1021/Acs.Orglett.0C00300 |
0.561 |
|
| 2020 |
Lai Z, Zhang R, Feng Q, Sun J. 3-Aminooxetanes: versatile 1,3-amphoteric molecules for intermolecular annulation reactions Chemical Science. DOI: 10.1039/D0Sc04254D |
0.431 |
|
| 2020 |
Wu A, Qian H, Zhao W, Sun J. Benzannulation of isobenzopyryliums with electron-rich alkynes: a modular access to β-functionalized naphthalenes Chemical Science. 11: 7957-7962. DOI: 10.1039/D0Sc02502J |
0.455 |
|
| 2020 |
Wu A, Zhao W, Sun J. Synthesis of medium-sized lactones from siloxy alkynes via ring expansion Tetrahedron. 131163. DOI: 10.1016/J.Tet.2020.131163 |
0.52 |
|
| 2019 |
Huang H, Yang W, Chen Z, Lai Z, Sun J. A mild catalytic synthesis of 2-oxazolines oxetane ring-opening: rapid access to a diverse family of natural products. Chemical Science. 10: 9586-9590. PMID 32055332 DOI: 10.1039/C9Sc03843D |
0.537 |
|
| 2019 |
Zou X, Sun G, Huang H, Wang J, Yang W, Sun J. Catalytic Enantioselective Synthesis of 1,4-Benzodioxepines. Organic Letters. PMID 31840516 DOI: 10.1021/Acs.Orglett.9B04244 |
0.596 |
|
| 2019 |
Song L, Feng Q, Wang Y, Ding S, Wu YD, Zhang X, Chung LW, Sun J. Ru-Catalyzed Migratory Geminal Semi-Hydrogenation of Internal Alkynes to Terminal Olefins. Journal of the American Chemical Society. PMID 31596081 DOI: 10.1021/Jacs.9B09658 |
0.644 |
|
| 2019 |
Zhang R, Guo W, Duan M, Houk KN, Sun J. Asymmetric Desymmetrization of Oxetanes for the Synthesis of Chiral Tetrahydrothiophenes and Tetrahydroselenophenes. Angewandte Chemie (International Ed. in English). PMID 31549762 DOI: 10.1002/Anie.201910917 |
0.587 |
|
| 2019 |
Chen M, Qian D, Sun J. Organocatalytic Enantioconvergent Synthesis of Tetrasubstituted Allenes via Asymmetric 1,8-Addition to aza--Quinone Methides. Organic Letters. PMID 31544464 DOI: 10.1021/Acs.Orglett.9B03224 |
0.584 |
|
| 2019 |
Ma D, Miao CB, Sun J. Catalytic Enantioselective House‒Meinwald Rearrangement: Efficient Construction of All-Carbon Quaternary Stereocenters. Journal of the American Chemical Society. PMID 31429560 DOI: 10.1021/Jacs.9B07514 |
0.537 |
|
| 2019 |
Ma D, Zhang Z, Chen M, Lin Z, Sun J. Organocatalytic Enantioselective Functionalization of Unactivated Indole C(sp3)-H Bonds. Angewandte Chemie (International Ed. in English). PMID 31424147 DOI: 10.1002/Anie.201909397 |
0.504 |
|
| 2019 |
Wu A, Feng Q, Sung HHY, Williams ID, Sun J. Synthesis of Eight-Membered Lactams via Formal [6+2] Cyclization of Siloxy Alkynes and Vinylazetidines. Angewandte Chemie (International Ed. in English). PMID 30888103 DOI: 10.1002/Anie.201902866 |
0.586 |
|
| 2019 |
Zhang Z, Yan J, Ma D, Sun J. Electrochemical synthesis of β-hydroxy-, β-alkoxy-, and β-carbonyloxy sulfones by vicinal difunctionalization of olefins Chinese Chemical Letters. 30: 1509-1511. DOI: 10.1016/J.Cclet.2019.04.023 |
0.36 |
|
| 2019 |
Qian D, Sun J. Frontispiece: Recent Progress in Asymmetric Ion‐Pairing Catalysis with Ammonium Salts Chemistry – a European Journal. 25. DOI: 10.1002/Chem.201981564 |
0.395 |
|
| 2018 |
Qian D, Sun J. Recent Progress on Asymmetric Ion-Pairing Catalysis on Ammoniums. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30358913 DOI: 10.1002/Chem.201803752 |
0.526 |
|
| 2018 |
Zhao W, Sun J. Triflimide (HNTf) in Organic Synthesis. Chemical Reviews. PMID 30251840 DOI: 10.1021/Acs.Chemrev.8B00279 |
0.471 |
|
| 2018 |
Yang W, Ma D, Zhou Y, Dong X, Lin Z, Sun J. NHC-Catalyzed Electrophilic Trifluoromethylation: Efficient Synthesis of γ-Trifluoromethyl α,β-Unsaturated Esters. Angewandte Chemie (International Ed. in English). PMID 30016564 DOI: 10.1002/Anie.201806674 |
0.519 |
|
| 2018 |
Liu B, Wang Y, Chen Y, Wu Q, Zhao J, Sun J. Stereoselective Synthesis of Fully-Substituted Acrylonitriles via Formal Acylcyanation of Electron-Rich Alkynes. Organic Letters. PMID 29873500 DOI: 10.1021/Acs.Orglett.8B01180 |
0.547 |
|
| 2018 |
Yan J, Chen M, Sung HH, Williams ID, Sun J. An Organocatalytic Asymmetric Synthesis of Chiral β,β-Diaryl-α-amino Acids via Addition of Azlactones to In-Situ Generated para-Quinone Methides. Chemistry, An Asian Journal. PMID 29806138 DOI: 10.1002/Asia.201800569 |
0.474 |
|
| 2018 |
Qian D, Chen M, Bissember AC, Sun J. Counterion-Induced Asymmetric Control on Azetidiniums: A Facile Access to Chiral Amines. Angewandte Chemie (International Ed. in English). PMID 29431882 DOI: 10.1002/Anie.201712395 |
0.75 |
|
| 2018 |
Wu A, Sun J. A [3+2] Cyclization of Siloxyalkynes and Isocyanides for the Synthesis of Oxazoles Synlett. 30: 515-518. DOI: 10.1055/S-0037-1610402 |
0.574 |
|
| 2018 |
Chen M, Han Y, Ma D, Wang Y, Lai Z, Sun J. Organocatalytic Enantioselective Synthesis of Chiral Diarylmethylamines from Racemic Alcohols Chinese Journal of Chemistry. 36: 587-593. DOI: 10.1002/Cjoc.201800135 |
0.428 |
|
| 2017 |
Qian D, Wu L, Lin Z, Sun J. Organocatalytic synthesis of chiral tetrasubstituted allenes from racemic propargylic alcohols. Nature Communications. 8: 567. PMID 28924216 DOI: 10.1038/S41467-017-00251-X |
0.567 |
|
| 2017 |
Chen M, Sun J. Understanding the Role of Additive Leads to an Improved Synthetic Protocol Obviating Additive: Organocatalytic Synthesis of Chiral Diarylmethyl Alkynes. Angewandte Chemie (International Ed. in English). PMID 28722279 DOI: 10.1002/Anie.201706579 |
0.548 |
|
| 2017 |
Wang Z, Sun J. Enantioselective [4 + 2] Cycloaddition of o-Quinone Methides and Vinyl Sulfides: Indirect Access to Generally Substituted Chiral Chromanes. Organic Letters. PMID 28445070 DOI: 10.1021/Acs.Orglett.7B00867 |
0.834 |
|
| 2017 |
Chen M, Sun J. Catalytic Asymmetric N-Alkylation of Indoles and Carbazoles through 1,6-Conjugate Addition of Aza-para-quinone Methides. Angewandte Chemie (International Ed. in English). PMID 28332764 DOI: 10.1002/Anie.201701947 |
0.543 |
|
| 2016 |
Yang W, Hu W, Dong X, Li X, Sun J. N-Heterocyclic Carbene Catalyzed γ-Dihalomethylenation of Enals by Single-Electron Transfer. Angewandte Chemie (International Ed. in English). PMID 27873395 DOI: 10.1002/Anie.201608371 |
0.452 |
|
| 2016 |
Li H, Tong R, Sun J. Catalytic Enantioselective Aza-Piancatelli Rearrangement. Angewandte Chemie (International Ed. in English). PMID 27785871 DOI: 10.1002/Anie.201607714 |
0.579 |
|
| 2016 |
Wang Y, Song LJ, Zhang X, Sun J. Metal-Free [2+2+2] Cycloaddition of Ynamides and Nitriles: Mild and Regioselective Synthesis of Fully Substituted Pyridines. Angewandte Chemie (International Ed. in English). PMID 27381408 DOI: 10.1002/Anie.201603889 |
0.513 |
|
| 2016 |
Song LJ, Ding S, Wang Y, Zhang X, Wu YD, Sun J. Ir-Catalyzed Regio- and Stereoselective Hydrosilylation of Internal Thioalkynes: A Combined Experimental and Computational Study. The Journal of Organic Chemistry. PMID 27232905 DOI: 10.1021/Acs.Joc.6B00854 |
0.665 |
|
| 2016 |
Yang W, Wang Z, Sun J. Enantioselective Oxetane Ring Opening with Chloride: Unusual Use of Wet Molecular Sieves for the Controlled Release of HCl. Angewandte Chemie (International Ed. in English). PMID 27122466 DOI: 10.1002/Anie.201601844 |
0.781 |
|
| 2016 |
Wong YF, Wang Z, Sun J. Chiral phosphoric acid catalyzed asymmetric addition of naphthols to para-quinone methides. Organic & Biomolecular Chemistry. PMID 26932597 DOI: 10.1039/C6Ob00125D |
0.81 |
|
| 2016 |
Wang Z, Hong W, Sun J. Organocatalytic Enantioselective Desymmetrization of meso-Aziridines and Prochiral Azetidines Current Organic Chemistry. 20: 1851-1861. DOI: 10.2174/1385272820666160331235258 |
0.83 |
|
| 2016 |
Wang Z, Hong W, Sun J. ChemInform Abstract: Organocatalytic Enantioselective Desymmetrization of Meso-Aziridines and Prochiral Azetidines Cheminform. 47. DOI: 10.1002/chin.201643216 |
0.404 |
|
| 2016 |
Lai Z, Sun J. ChemInform Abstract: Enantioselective Addition of Thiols to ortho-Quinone Methides Catalyzed by Chiral Phosphoric Acids. Cheminform. 47. DOI: 10.1002/chin.201628106 |
0.435 |
|
| 2016 |
Wang Z, Sun J. ChemInform Abstract: Recent Advances in Catalytic Asymmetric Reactions of o-Quinone Methides Cheminform. 47: no-no. DOI: 10.1002/chin.201607253 |
0.353 |
|
| 2015 |
Yang W, Sun J. Organocatalytic Enantioselective Synthesis of 1,4-Dioxanes and Other Oxa-Heterocycles by Oxetane Desymmetrization. Angewandte Chemie (International Ed. in English). PMID 26689744 DOI: 10.1002/Anie.201509888 |
0.57 |
|
| 2015 |
Lai Z, Wang Z, Sun J. Organocatalytic Asymmetric Nucleophilic Addition to o-Quinone Methides by Alcohols. Organic Letters. PMID 26637015 DOI: 10.1021/Acs.Orglett.5B03072 |
0.793 |
|
| 2015 |
Wang Z, Wong YF, Sun J. Catalytic Asymmetric 1,6-Conjugate Addition of para-Quinone Methides: Formation of All-Carbon Quaternary Stereocenters. Angewandte Chemie (International Ed. in English). PMID 26403542 DOI: 10.1002/Anie.201506701 |
0.818 |
|
| 2015 |
Zhao W, Qian H, Li Z, Sun J. Catalytic Ring Expansion of Cyclic Hemiaminals for the Synthesis of Medium-Ring Lactams. Angewandte Chemie (International Ed. in English). PMID 26136349 DOI: 10.1002/Anie.201504926 |
0.53 |
|
| 2015 |
Wang Z, Sheong FK, Sung HH, Williams ID, Lin Z, Sun J. Catalytic enantioselective intermolecular desymmetrization of azetidines. Journal of the American Chemical Society. 137: 5895-8. PMID 25921194 DOI: 10.1021/Jacs.5B03083 |
0.833 |
|
| 2015 |
Ding S, Song LJ, Wang Y, Zhang X, Chung LW, Wu YD, Sun J. Highly Regio- and Stereoselective Hydrosilylation of Internal Thioalkynes under Mild Conditions. Angewandte Chemie (International Ed. in English). 54: 5632-5. PMID 25784284 DOI: 10.1002/Anie.201500372 |
0.652 |
|
| 2015 |
Qian H, Zhao W, Wang Z, Sun J. Organocatalytic enantio- and diastereoselective synthesis of 1,2-dihydronaphthalenes from isobenzopyrylium ions. Journal of the American Chemical Society. 137: 560-3. PMID 25551644 DOI: 10.1021/Ja509824J |
0.838 |
|
| 2015 |
Wang Z, Ai F, Wang Z, Zhao W, Zhu G, Lin Z, Sun J. Organocatalytic asymmetric synthesis of 1,1-diarylethanes by transfer hydrogenation. Journal of the American Chemical Society. 137: 383-9. PMID 25482291 DOI: 10.1021/Ja510980D |
0.822 |
|
| 2015 |
Dong X, Yang W, Hu W, Sun J. N-heterocyclic carbene catalyzed enantioselective α-fluorination of aliphatic aldehydes and α-chloro aldehydes: synthesis of α-fluoro esters, amides, and thioesters. Angewandte Chemie (International Ed. in English). 54: 660-3. PMID 25394812 DOI: 10.1002/Anie.201409961 |
0.487 |
|
| 2015 |
Zhao W, Wang Z, Chu B, Sun J. Enantioselective formation of all-carbon quaternary stereocenters from indoles and tertiary alcohols bearing a directing group. Angewandte Chemie (International Ed. in English). 54: 1910-3. PMID 25088146 DOI: 10.1002/Anie.201405252 |
0.808 |
|
| 2015 |
Lai Z, Sun J. Enantioselective Addition of Thiols to ortho-Quinone Methides Catalyzed by Chiral Phosphoric Acids Synlett. DOI: 10.1055/S-0035-1560546 |
0.553 |
|
| 2015 |
Sun J, Wang Z. Recent Advances in Catalytic Asymmetric Reactions of o-Quinone Methides Synthesis. 47: e7-e7. DOI: 10.1055/S-0035-1560370 |
0.82 |
|
| 2015 |
Wong YF, Wang Z, Hong WX, Sun J. A one-pot oxidation/cycloaddition cascade synthesis of 2,4-diaryl chromans via ortho-quinone methides Tetrahedron. DOI: 10.1016/J.Tet.2015.12.011 |
0.78 |
|
| 2014 |
Luo Q, Jia G, Sun J, Lin Z. Theoretical studies on the regioselectivity of iridium-catalyzed 1,3-dipolar azide-alkyne cycloaddition reactions. The Journal of Organic Chemistry. 79: 11970-80. PMID 25222638 DOI: 10.1021/Jo5018348 |
0.514 |
|
| 2014 |
Qian H, Zhao W, Sun J. Siloxy alkynes in annulation reactions. Chemical Record (New York, N.Y.). 14: 1070-85. PMID 25171137 DOI: 10.1002/Tcr.201402042 |
0.539 |
|
| 2014 |
Wang Z, Chen Z, Sun J. Catalytic asymmetric nucleophilic openings of 3-substituted oxetanes. Organic & Biomolecular Chemistry. 12: 6028-32. PMID 24968137 DOI: 10.1039/C4Ob00920G |
0.837 |
|
| 2014 |
Dong X, Sun J. Catalytic asymmetric α-aldol reaction of vinylogous N-heterocyclic carbene enolates: formation of quaternary and labile tertiary stereocenters. Organic Letters. 16: 2450-3. PMID 24725090 DOI: 10.1021/Ol500830A |
0.49 |
|
| 2014 |
Ding S, Jia G, Sun J. Iridium-catalyzed intermolecular azide-alkyne cycloaddition of internal thioalkynes under mild conditions. Angewandte Chemie (International Ed. in English). 53: 1877-80. PMID 24474668 DOI: 10.1002/Anie.201309855 |
0.639 |
|
| 2014 |
Zhao W, Sun J. New Strategies for medium- and large-ring lactone synthesis Synlett. 25: 303-307. DOI: 10.1055/S-0033-1340308 |
0.497 |
|
| 2014 |
Zhao W, Sun J. ChemInform Abstract: New Strategies for Medium- and Large-Ring Lactone Synthesis Cheminform. 45: no-no. DOI: 10.1002/chin.201428239 |
0.31 |
|
| 2014 |
Qian H, Sun J. Organocatalytic enantio- and diastereoselective assembly of thiazolidine scaffolds by formal [3+2] annulation Asian Journal of Organic Chemistry. 3: 387-390. DOI: 10.1002/Ajoc.201400025 |
0.554 |
|
| 2013 |
Chen Z, Sun J. Enantio- and diastereoselective assembly of tetrahydrofuran and tetrahydropyran skeletons with all-carbon-substituted quaternary stereocenters. Angewandte Chemie (International Ed. in English). 52: 13593-6. PMID 24254193 DOI: 10.1002/Anie.201306801 |
0.487 |
|
| 2013 |
Qian H, Yu X, Zhang J, Sun J. Organocatalytic enantioselective synthesis of 2,3-allenoates by intermolecular addition of nitroalkanes to activated enynes. Journal of the American Chemical Society. 135: 18020-3. PMID 24224493 DOI: 10.1021/Ja409080V |
0.563 |
|
| 2013 |
Wang Z, Law WK, Sun J. Chiral phosphoric acid catalyzed enantioselective desymmetrization of meso-epoxides by thiols. Organic Letters. 15: 5964-6. PMID 24219853 DOI: 10.1021/Ol402797V |
0.842 |
|
| 2013 |
Ding S, Song LJ, Chung LW, Zhang X, Sun J, Wu YD. Ligand-controlled remarkable regio- and stereodivergence in intermolecular hydrosilylation of internal alkynes: experimental and theoretical studies. Journal of the American Chemical Society. 135: 13835-42. PMID 23971888 DOI: 10.1021/Ja405752W |
0.615 |
|
| 2013 |
Wang Z, Chen Z, Sun J. Catalytic enantioselective intermolecular desymmetrization of 3-substituted oxetanes. Angewandte Chemie (International Ed. in English). 52: 6685-8. PMID 23681611 DOI: 10.1002/Anie.201300188 |
0.833 |
|
| 2013 |
Chen Z, Wang Z, Sun J. Catalytic enantioselective synthesis of tetrahydroisoquinolines and their analogues bearing a C4 stereocenter: formal synthesis of (+)-(8S,13R)-cyclocelabenzine. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 8426-30. PMID 23677731 DOI: 10.1002/Chem.201301065 |
0.796 |
|
| 2013 |
Zhao W, Li Z, Sun J. A new strategy for efficient synthesis of medium and large ring lactones without high dilution or slow addition. Journal of the American Chemical Society. 135: 4680-3. PMID 23472580 DOI: 10.1021/Ja400883Q |
0.467 |
|
| 2013 |
Chen Z, Wang B, Wang Z, Zhu G, Sun J. Complex bioactive alkaloid-type polycycles through efficient catalytic asymmetric multicomponent aza-Diels-Alder reaction of indoles with oxetane as directing group. Angewandte Chemie (International Ed. in English). 52: 2027-31. PMID 23303578 DOI: 10.1002/Anie.201206481 |
0.806 |
|
| 2013 |
Qian H, Zhao W, Sung HH, Williams ID, Sun J. Stereoselective synthesis of aminoindanols via an efficient cascade aza-Michael-aldol reaction. Chemical Communications (Cambridge, England). 49: 4361-3. PMID 23169191 DOI: 10.1039/C2Cc37102B |
0.52 |
|
| 2013 |
Dong X, Zhao YM, Sun J. N-heterocyclic carbene (NHC) catalyzed synthesis of α,α- difluoro esters Synlett. 24: 1221-1224. DOI: 10.1055/S-0033-1338955 |
0.438 |
|
| 2013 |
Wang Z, Chen Z, Sun J. Cover Picture: Catalytic Enantioselective Intermolecular Desymmetrization of 3-Substituted Oxetanes (Angew. Chem. Int. Ed. 26/2013) Angewandte Chemie International Edition. 52: 6547-6547. DOI: 10.1002/Anie.201304412 |
0.816 |
|
| 2013 |
Wang Z, Chen Z, Sun J. Titelbild: Catalytic Enantioselective Intermolecular Desymmetrization of 3-Substituted Oxetanes (Angew. Chem. 26/2013) Angewandte Chemie. 125: 6677-6677. DOI: 10.1002/Ange.201304412 |
0.832 |
|
| 2012 |
Zhao YM, Cheung MS, Lin Z, Sun J. Enantioselective synthesis of β,γ-unsaturated α-fluoroesters catalyzed by N-heterocyclic carbenes. Angewandte Chemie (International Ed. in English). 51: 10359-63. PMID 22965929 DOI: 10.1002/Anie.201204521 |
0.395 |
|
| 2012 |
Zhao W, Wang Z, Sun J. Synthesis of eight-membered lactones: intermolecular [6+2] cyclization of amphoteric molecules with siloxy alkynes. Angewandte Chemie (International Ed. in English). 51: 6209-13. PMID 22588830 DOI: 10.1002/Anie.201200513 |
0.792 |
|
| 2012 |
Zhao YM, Tam Y, Wang YJ, Li Z, Sun J. N-heterocyclic carbene-catalyzed internal redox reaction of alkynals: an efficient synthesis of allenoates. Organic Letters. 14: 1398-401. PMID 22352302 DOI: 10.1021/Ol300111M |
0.568 |
|
| 2012 |
Oelke AJ, Sun J, Fu GC. Nickel-catalyzed enantioselective cross-couplings of racemic secondary electrophiles that bear an oxygen leaving group. Journal of the American Chemical Society. 134: 2966-9. PMID 22296603 DOI: 10.1021/Ja300031W |
0.731 |
|
| 2012 |
Fan T, Chen X, Sun J, Lin Z. DFT studies on gold-catalyzed cycloisomerization of 1,5-enynes Organometallics. 31: 4221-4227. DOI: 10.1021/Om300167U |
0.38 |
|
| 2011 |
Fujiwara Y, Sun J, Fu GC. Enantioselective Carbon-Sulfur Bond Formation: γ Additions of Aryl Thiols to Allenoates Catalyzed by a Chiral Phosphepine. Chemical Science (Royal Society of Chemistry : 2010). 2: 2196-2198. PMID 22216403 DOI: 10.1039/C1Sc00414J |
0.779 |
|
| 2010 |
Sun J, Keller VA, Meyer ST, Kozmin SA. Silver-Catalyzed Aldehyde Olefination Using Siloxy Alkynes. Advanced Synthesis & Catalysis. 352. PMID 24273478 DOI: 10.1002/Adsc.200900835 |
0.776 |
|
| 2010 |
Sinisi R, Sun J, Fu GC. Phosphine-catalyzed asymmetric additions of malonate esters to {gamma}-substituted allenoates and allenamides. Proceedings of the National Academy of Sciences of the United States of America. 107: 20652-4. PMID 20624987 DOI: 10.1073/Pnas.1003597107 |
0.735 |
|
| 2010 |
Sun J, Fu GC. Phosphine-catalyzed formation of carbon-sulfur bonds: catalytic asymmetric synthesis of gamma-thioesters. Journal of the American Chemical Society. 132: 4568-9. PMID 20222657 DOI: 10.1021/Ja101251D |
0.731 |
|
| 2010 |
Wilson JE, Sun J, Fu GC. Stereoselective phosphine-catalyzed synthesis of highly functionalized diquinanes. Angewandte Chemie (International Ed. in English). 49: 161-3. PMID 19943302 DOI: 10.1002/Anie.200905125 |
0.784 |
|
| 2010 |
Sun J, Fu GC. ChemInform Abstract: Phosphine-Catalyzed Formation of Carbon-Sulfur Bonds: Catalytic Asymmetric Synthesis of γ-Thioesters. Cheminform. 41: no-no. DOI: 10.1002/chin.201030051 |
0.704 |
|
| 2009 |
Cheng C, Sun J, Xing L, Xu J, Wang X, Hu Y. Highly chemoselective Pd-C catalytic hydrodechlorination leading to the highly efficient N-debenzylation of benzylamines. The Journal of Organic Chemistry. 74: 5671-4. PMID 19534475 DOI: 10.1021/Jo9007282 |
0.606 |
|
| 2007 |
Cao L, Sun J, Wang X, Zhu R, Shi H, Hu Y. Total synthesis of (−)-elegansidiol by using an abnormal Beckmann fragmentation of Hajos ketone oxime as a key step Tetrahedron. 63: 5036-5041. DOI: 10.1016/J.Tet.2007.03.123 |
0.651 |
|
| 2007 |
Cao L, Sun J, Wang X, Zhu R, Shi H, Hu Y. Total Synthesis of (-)-Elegansidiol (IV) by Using an Abnormal Beckmann Fragmentation of Hajos Ketone Oxime as a Key Step. Cheminform. 38. DOI: 10.1002/chin.200737174 |
0.63 |
|
| 2007 |
Zhang L, Sun J, Kozmin SA. Broensted Acid Promoted Cyclizations of Siloxy Alkynes with Unactivated Arenes, Alkenes, and Alkynes. Cheminform. 38. DOI: 10.1002/chin.200710039 |
0.344 |
|
| 2006 |
Sun J, Conley MP, Zhang L, Kozmin SA. Au- and pt-catalyzed cycloisomerizations of 1,5-enynes to cyclohexadienes with a broad alkyne scope. Journal of the American Chemical Society. 128: 9705-10. PMID 16866525 DOI: 10.1021/Ja063384N |
0.77 |
|
| 2006 |
Sun J, Kozmin SA. Silver-catalyzed hydroamination of siloxy alkynes. Angewandte Chemie (International Ed. in English). 45: 4991-3. PMID 16810653 DOI: 10.1002/Anie.200601276 |
0.731 |
|
| 2006 |
Zhang L, Sun J, Kozmin SA. Brønsted acid-promoted cyclizations of siloxy alkynes with unactivated arenes, alkenes, and alkynes Tetrahedron. 62: 11371-11380. DOI: 10.1016/J.Tet.2006.06.037 |
0.731 |
|
| 2006 |
Zhang L, Sun J, Kozmin SA. Gold and platinum catalysis of enyne cycloisomerization Advanced Synthesis and Catalysis. 348: 2271-2296. DOI: 10.1002/Adsc.200600368 |
0.7 |
|
| 2005 |
Sun J, Kozmin SA. Brønsted acid-promoted cyclizations of 1-siloxy-1,5-diynes. Journal of the American Chemical Society. 127: 13512-3. PMID 16190711 DOI: 10.1021/Ja055054T |
0.716 |
|
| 2005 |
Wang X, Dong Y, Sun J, Xu X, Li R, Hu Y. Nonracemic Betti base as a new chiral auxiliary: application to total syntheses of enantiopure (2S,6R)-dihydropinidine and (2S,6R)-isosolenopsins. The Journal of Organic Chemistry. 70: 1897-900. PMID 15730317 DOI: 10.1021/Jo0480444 |
0.618 |
|
| 2005 |
Wang S, Cao L, Shi H, Dong Y, Sun J, Hu Y. Preparation of 2-pyridone-containing tricyclic alkaloid derivatives as potential inhibitors of tumor cell proliferation by regioselective intramolecular N- and C-acylation of 2-pyridone. Chemical & Pharmaceutical Bulletin. 53: 67-71. PMID 15635233 DOI: 10.1248/Cpb.53.67 |
0.624 |
|
| 2004 |
Sun J, Dong Y, Cao L, Wang X, Wang S, Hu Y. Highly efficient chemoselective deprotection of O,O-acetals and O,O-ketals catalyzed by molecular iodine in acetone. The Journal of Organic Chemistry. 69: 8932-4. PMID 15575776 DOI: 10.1021/Jo0486239 |
0.598 |
|
| 2004 |
Wang S, Sun J, Yu G, Hu X, Liu JO, Hu Y. CuI catalyzed N-arylation of amide as a key step for the preparation of 3-aryl beta-carbolin-1-ones. Organic & Biomolecular Chemistry. 2: 1573-4. PMID 15162205 DOI: 10.1039/B406046F |
0.641 |
|
| 2004 |
Dong Y, Sun J, Wang X, Xu X, Chao L, Hu Y. Highly Regioselective N-Alkylation of Nonracemic Betti Base: A Novel One-Pot Synthesis of Chiral N-Methyl-N-alkyl Betti Bases. Cheminform. 35. DOI: 10.1016/J.Tetasy.2004.04.006 |
0.615 |
|
| 2004 |
Dong Y, Sun J, Wang X, Xu X, Cao L, Hu Y. Highly regioselective N-alkylation of nonracemic Betti base: a novel one-pot synthesis of chiral N-methyl-N-alkyl Betti bases Tetrahedron: Asymmetry. 15: 1667-1672. DOI: 10.1016/j.tetasy.2004.04.006 |
0.577 |
|
| 2001 |
Sinha SC, Sun J, Miller GP, Wartmann M, Lerner RA. Catalytic antibody route to the naturally occurring epothilones: total synthesis of epothilones A-F. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 1691-702. PMID 11349910 DOI: 10.1002/1521-3765(20010417)7:8<1691::Aid-Chem16910>3.0.Co;2-9 |
0.315 |
|
| Show low-probability matches. |