| Year |
Citation |
Score |
| 2024 |
Dai L, Zhou X, Guo J, Huang Q, Lu Y. Copper-catalyzed atroposelective synthesis of C-O axially chiral compounds enabled by chiral 1,8-naphthyridine based ligands. Chemical Science. 15: 5993-6001. PMID 38665510 DOI: 10.1039/d4sc01074d |
0.441 |
|
| 2024 |
Liu WQ, Lee BC, Song N, He Z, Shen ZA, Lu Y, Koh MJ. Electrochemical Synthesis of C(sp3)-Rich Amines by Aminative Carbofunctionalization of Carbonyl Compounds. Angewandte Chemie (International Ed. in English). e202402140. PMID 38650440 DOI: 10.1002/anie.202402140 |
0.448 |
|
| 2024 |
Zhou X, Huang Q, Guo J, Dai L, Lu Y. Catalytic Asymmetric Construction of α,α-Diaryl Aldehydes via Oxo-Hydroarylation of Terminal Alkynes. Advanced Science (Weinheim, Baden-Wurttemberg, Germany). e2309645. PMID 38650176 DOI: 10.1002/advs.202309645 |
0.403 |
|
| 2024 |
Zheng W, Tan BB, Ge S, Lu Y. Enantioselective Copper-Catalyzed Ring-Opening Diboration of Arylidenecyclopropanes to Access Chiral Skipped 1,4- and 1,3-Diboronates. Journal of the American Chemical Society. 146: 5366-5374. PMID 38354313 DOI: 10.1021/jacs.3c12675 |
0.483 |
|
| 2023 |
Zhou X, Huang Q, Guo J, Dai L, Lu Y. Molecular Editing of Pyrroles via a Skeletal Recasting Strategy. Acs Central Science. 9: 1758-1767. PMID 37780359 DOI: 10.1021/acscentsci.3c00812 |
0.353 |
|
| 2023 |
Zhou X, Huang Q, Guo J, Dai L, Lu Y. Enantioselective De Novo Synthesis of α,α-Diaryl Ketones from Alkynes. Angewandte Chemie (International Ed. in English). 62: e202310078. PMID 37724448 DOI: 10.1002/anie.202310078 |
0.368 |
|
| 2023 |
Dai L, Zhou X, Guo J, Dai X, Huang Q, Lu Y. Diastereo- and atroposelective synthesis of N-arylpyrroles enabled by light-induced phosphoric acid catalysis. Nature Communications. 14: 4813. PMID 37558716 DOI: 10.1038/s41467-023-40491-8 |
0.425 |
|
| 2022 |
Tan CXA, Li R, Zhang F, Dai L, Ullah N, Lu Y. Synthesis of Axially Chiral CF3-Substituted 2-Arylpyrroles by Sequential Phosphine-Catalyzed Asymmetric [3+2] Annulation and Oxidative Central-to-Axial Chirality Transfer. Angewandte Chemie (International Ed. in English). PMID 36200408 DOI: 10.1002/anie.202209494 |
0.436 |
|
| 2022 |
Huang Q, Zhou X, Dai L, Chen Y, Lu Y. Nickel-Hydride-Catalyzed Diastereo- and Enantioselective Hydroalkylation of Cyclopropenes. Angewandte Chemie (International Ed. in English). PMID 36124410 DOI: 10.1002/anie.202210560 |
0.5 |
|
| 2022 |
Dai L, Guo J, Huang Q, Lu Y. Asymmetric multifunctionalization of alkynes via photo-irradiated organocatalysis. Science Advances. 8: eadd2574. PMID 36103531 DOI: 10.1126/sciadv.add2574 |
0.379 |
|
| 2022 |
Wang N, Lang Y, Wang J, Wu Z, Lu Y. Phosphine-Catalyzed Sequential [3 + 2]/[3 + 2] Annulation between Allenoates and Arylidenemalononitriles for the Enantioselective Construction of Bicyclo[3,3,0]octenes and Cyclopenta[]quinolinones. Organic Letters. PMID 35584054 DOI: 10.1021/acs.orglett.2c01352 |
0.419 |
|
| 2022 |
Bai X, Zheng W, Ge S, Lu Y. Enantioselective Palladium-Catalyzed Arylborylation/Cyclization of Alkenes to Access Boryl-Functionalized Heterocyclic Compounds Containing Quaternary Stereogenic Centers. Organic Letters. PMID 35436402 DOI: 10.1021/acs.orglett.2c01082 |
0.538 |
|
| 2022 |
Wu M, Han Z, Ni H, Wang N, Ding K, Lu Y. Phosphine-catalyzed divergent domino processes between γ-substituted allenoates and carbonyl-activated alkenes. Chemical Science. 13: 3161-3168. PMID 35414887 DOI: 10.1039/d1sc06364b |
0.519 |
|
| 2022 |
Zhang F, Dai X, Dai L, Zheng W, Chan WL, Tang X, Zhang X, Lu Y. Phosphine-Catalyzed Enantioselective (3+2) Annulation of Vinylcyclopropanes with Imines for the Synthesis of Chiral Pyrrolidines. Angewandte Chemie (International Ed. in English). e202203212. PMID 35357071 DOI: 10.1002/anie.202203212 |
0.763 |
|
| 2021 |
Chen Y, Zhu K, Huang Q, Lu Y. Regiodivergent sulfonylarylation of 1,3-enynes nickel/photoredox dual catalysis. Chemical Science. 12: 13564-13571. PMID 34777776 DOI: 10.1039/d1sc04320j |
0.477 |
|
| 2021 |
Chen Y, Wang J, Lu Y. Decarboxylative 1,4-carbocyanation of 1,3-enynes to access tetra-substituted allenes copper/photoredox dual catalysis. Chemical Science. 12: 11316-11321. PMID 34667542 DOI: 10.1039/d1sc02896k |
0.358 |
|
| 2021 |
Wang N, Wu Z, Wang J, Ullah N, Lu Y. Recent applications of asymmetric organocatalytic annulation reactions in natural product synthesis. Chemical Society Reviews. PMID 34286704 DOI: 10.1039/d0cs01124j |
0.364 |
|
| 2021 |
Zhang F, Zeng J, Gao M, Wang L, Chen GQ, Lu Y, Zhang X. Concise, scalable and enantioselective total synthesis of prostaglandins. Nature Chemistry. PMID 34045714 DOI: 10.1038/s41557-021-00706-1 |
0.373 |
|
| 2021 |
Mei GJ, Koay WL, Tan CXA, Lu Y. Catalytic asymmetric preparation of pyrroloindolines: strategies and applications to total synthesis. Chemical Society Reviews. 50: 5985-6012. PMID 34027944 DOI: 10.1039/d0cs00530d |
0.323 |
|
| 2021 |
Alvin Tan CX, Mei GJ, Lu Y. Phosphine-Catalyzed Asymmetric Allylic Alkylation of Achiral MBH Carbonates with 3,3'-Bisindolines: Enantioselective Construction of Quaternary Stereogenic Centers. Organic Letters. PMID 33615793 DOI: 10.1021/acs.orglett.1c00201 |
0.425 |
|
| 2020 |
Tasdan Y, Mei GJ, Lu Y. Enantioselective synthesis of mixed 3,3'-bisindoles via a phosphine-catalyzed umpolung γ-addition of 3'-indolyl-3-oxindoles to allenoates. Science Bulletin. 65: 557-563. PMID 36659187 DOI: 10.1016/j.scib.2020.01.017 |
0.597 |
|
| 2020 |
Ni H, Wong YL, Wu M, Han Z, Ding K, Lu Y. Highly Enantioselective [3 + 2] Annulation of 3-Butynoates with β-Trifluoromethyl Enones Promoted by an Amine-Phosphine Binary Catalytic System. Organic Letters. PMID 32155074 DOI: 10.1021/Acs.Orglett.0C00681 |
0.617 |
|
| 2020 |
Mei GJ, Zheng W, Gonçalves TP, Tang X, Huang KW, Lu Y. Catalytic Asymmetric Formal [3+2] Cycloaddition of Azoalkenes with 3-Vinylindoles: Synthesis of 2,3-Dihydropyrroles. Iscience. 23: 100873. PMID 32062452 DOI: 10.1016/J.Isci.2020.100873 |
0.584 |
|
| 2019 |
Lu Y, Bai X, Wu C, Ge S. Pd/Cu-Catalyzed Enantioselective Sequential Heck-Sonogashira Coupling: Asymmetric Synthesis of Oxindoles Containing Trifluoromethylated Quaternary Stereogenic Centers. Angewandte Chemie (International Ed. in English). PMID 31664752 DOI: 10.1002/Anie.201913148 |
0.598 |
|
| 2019 |
Lu Y, Mei GJ, Tang X, Tasdan Y. Enantioselective Dearomatization of Indoles via an Azoalkene-enabled (3+2) Reaction: Facile Access to Pyrroloindolines. Angewandte Chemie (International Ed. in English). PMID 31592562 DOI: 10.1002/Anie.201911686 |
0.567 |
|
| 2019 |
Wu M, Han Z, Li K, Wu J, Ding K, Lu Y. A Cyclohexyl-Fused Spirobiindane-derived Phosphine-catalyzed Synthesis of Tricyclic γ-Lactams and Kinetic Resolution of γ-Substituted Allenoates. Journal of the American Chemical Society. PMID 31545594 DOI: 10.1021/Jacs.9B07418 |
0.604 |
|
| 2019 |
Wang X, Lu M, Su Q, Zhou M, Addepalli Y, Yao W, Wang Z, Lu Y. Phosphine-catalyzed [4 + 2] cycloadditions of allenic ketones: Enantioselective synthesis of functionalized tetrahydropyridines. Chemistry, An Asian Journal. PMID 31508886 DOI: 10.1002/Asia.201901104 |
0.62 |
|
| 2019 |
Lu Y, Li K, Gonçalves TP, Huang KW. Dearomatization of 3-Nitroindoles via a Phosphine-catalyzed Enantioselective [3+2] Annulation Reaction. Angewandte Chemie (International Ed. in English). PMID 30770616 DOI: 10.1002/Anie.201900248 |
0.567 |
|
| 2019 |
Lu Y, Chan WL, Tang X, Zhang F, Quek G, Mei GJ. Phosphine-catalyzed (3+2) Annulation of Isoindigos with Allenes: Highly Enantioselective Creation of Two Vicinal Quaternary Stereogenic Centers. Angewandte Chemie (International Ed. in English). PMID 30746821 DOI: 10.1002/Anie.201900758 |
0.749 |
|
| 2019 |
Zhang J, Chan W, Chen L, Ullah N, Lu Y. Creation of bispiro[pyrazolone-3,3′-oxindoles] via a phosphine-catalyzed enantioselective [3 + 2] annulation of the Morita–Baylis–Hillman carbonates with pyrazoloneyldiene oxindoles Organic Chemistry Frontiers. 6: 2210-2214. DOI: 10.1039/C9Qo00471H |
0.509 |
|
| 2018 |
Ni H, Chan WL, Lu Y. Phosphine-Catalyzed Asymmetric Organic Reactions. Chemical Reviews. PMID 30204423 DOI: 10.1021/Acs.Chemrev.8B00261 |
0.718 |
|
| 2018 |
Jin Z, Ni H, Zhou B, Zheng W, Lu Y. Phosphine-Catalyzed Formal Oxa-[4 + 2] Annulation Employing Nitroethylene and Enones: Enantioselective Synthesis of Dihydropyrans. Organic Letters. PMID 30133289 DOI: 10.1021/Acs.Orglett.8B02519 |
0.616 |
|
| 2018 |
Yu Z, Jin Z, Duan M, Bai R, Lu Y, Lan Y. Toward a Predictive Understandings of Phosphine-Catalyzed [3+2] Annulation of Allenoates with Acrylate or Imine. The Journal of Organic Chemistry. PMID 30113828 DOI: 10.1021/Acs.Joc.8B01259 |
0.435 |
|
| 2018 |
Zhao Y, Kok GPY, Shao PL, Liao JY, Bte Sheikh Ismail SNF, Yao W, Lu Y. Divergent, Enantioselective Synthesis of Pyrroles, 3H Pyrroles and Bicyclic Imidazolines by Ag- or P-Catalyzed [3 + 2] Cycloaddition of Allenoates with Activated Isocyanides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29774613 DOI: 10.1002/Chem.201801768 |
0.605 |
|
| 2018 |
Han D, Chen Y, Wang S, Xiao M, Lu Y, Meng Y. Effect of In-Situ Dehydration on Activity and Stability of Cu–Ni–K2O/Diatomite as Catalyst for Direct Synthesis of Dimethyl Carbonate Catalysts. 8: 343. DOI: 10.3390/Catal8090343 |
0.477 |
|
| 2018 |
Han D, Chen Y, Wang S, Xiao M, Lu Y, Meng Y. Effect of Alkali-Doping on the Performance of Diatomite Supported Cu-Ni Bimetal Catalysts for Direct Synthesis of Dimethyl Carbonate Catalysts. 8: 302. DOI: 10.3390/Catal8080302 |
0.392 |
|
| 2018 |
Li K, Jin Z, Chan W, Lu Y. Enantioselective Construction of Bicyclic Pyran and Hydrindane Scaffolds via Intramolecular Rauhut–Currier Reactions Catalyzed by Thiourea-Phosphines Acs Catalysis. 8: 8810-8815. DOI: 10.1021/Acscatal.8B02706 |
0.566 |
|
| 2017 |
Ni H, Yu Z, Yao W, Lan Y, Ullah N, Lu Y. Catalyst-controlled regioselectivity in phosphine catalysis: the synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate. Chemical Science. 8: 5699-5704. PMID 28989609 DOI: 10.1039/C7Sc02176C |
0.523 |
|
| 2017 |
Yao W, Yu Z, Wen S, Ni H, Ullah N, Lan Y, Lu Y. Chiral phosphine-mediated intramolecular [3 + 2] annulation: enhanced enantioselectivity by achiral Brønsted acid. Chemical Science. 8: 5196-5200. PMID 28970906 DOI: 10.1039/C7Sc00952F |
0.528 |
|
| 2017 |
Lu Y, Ni H, Tang X, Zheng W, Yao W, Ullah N. Phosphine-catalyzed Enantioselective Formal [4+4] Annulation of alpha,beta-Unsaturated Imines and Allene Ketones: Construction of Eight-membered Rings. Angewandte Chemie (International Ed. in English). PMID 28816392 DOI: 10.1002/Anie.201707183 |
0.569 |
|
| 2017 |
Wang Z, Wang T, Yao W, Lu Y. Phosphine-Catalyzed Enantioselective [4 + 2] Annulation of o-Quinone Methides with Allene Ketones. Organic Letters. PMID 28723160 DOI: 10.1021/Acs.Orglett.7B01936 |
0.602 |
|
| 2017 |
Wang Z, Xu H, Su Q, Hu P, Shao PL, He Y, Lu Y. Enantioselective Synthesis of Tetrahydropyridines/Piperidines via Stepwise [4 + 2]/[2 + 2] Cyclizations. Organic Letters. PMID 28560873 DOI: 10.1021/Acs.Orglett.7B01221 |
0.586 |
|
| 2017 |
Li H, Lu Y. Enantioselective Construction of All‐Carbon Quaternary Stereogenic Centers by Using Phosphine Catalysis Asian Journal of Organic Chemistry. 6: 1130-1145. DOI: 10.1002/Ajoc.201700220 |
0.44 |
|
| 2017 |
Zhou B, Li K, Jiang C, Lu Y, Hayashi T. Modified Amino Acid-Derived Phosphine-Imine Ligands for Palladium-Catalyzed Asymmetric Arylation of Cyclic N
-Sulfonyl Imines Advanced Synthesis & Catalysis. 359: 1969-1975. DOI: 10.1002/Adsc.201700003 |
0.63 |
|
| 2016 |
Yao W, Dou X, Wen S, Wu J, Vittal JJ, Lu Y. Enantioselective desymmetrization of cyclohexadienones via an intramolecular Rauhut-Currier reaction of allenoates. Nature Communications. 7: 13024. PMID 27698487 DOI: 10.1038/Ncomms13024 |
0.773 |
|
| 2016 |
Lu Y, Zhou B, Jiang C, Gandi VR, Hayashi T. Palladium-Catalyzed Asymmetric Arylation for the Preparation of Trifluoromethylated/Perfluoroalkylated 2-Quinazolinone Derivatives with High (>99%) Enantioselectivity. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27377667 DOI: 10.1002/Chem.201603105 |
0.704 |
|
| 2016 |
Wang T, Han X, Zhong F, Yao W, Lu Y. Amino Acid-Derived Bifunctional Phosphines for Enantioselective Transformations. Accounts of Chemical Research. PMID 27310293 DOI: 10.1021/Acs.Accounts.6B00163 |
0.814 |
|
| 2016 |
Han X, Ni H, Chan WL, Gai X, Wang Y, Lu Y. Highly enantioselective synthesis of dihydrocoumarin-fused dihydropyrans via the phosphine-catalyzed [4 + 2] annulation of allenones with 3-aroylcoumarins. Organic & Biomolecular Chemistry. PMID 27173844 DOI: 10.1039/C6Ob00955G |
0.796 |
|
| 2016 |
Dou X, Lu Y, Hayashi T. Base-Free Conditions for Rhodium-Catalyzed Asymmetric Arylation To Produce Stereochemically Labile α-Aryl Ketones. Angewandte Chemie (International Ed. in English). PMID 27100902 DOI: 10.1002/Anie.201601709 |
0.802 |
|
| 2016 |
Ni H, Yao W, Waheed A, Ullah N, Lu Y. Enantioselective [4 + 2]-Annulation of Oxadienes and Allenones Catalyzed by an Amino Acid Derived Phosphine: Synthesis of Functionalized Dihydropyrans. Organic Letters. PMID 27091405 DOI: 10.1021/Acs.Orglett.6B00760 |
0.615 |
|
| 2016 |
Han X, Chan WL, Yao W, Wang Y, Lu Y. Phosphine-mediated Highly Enantioselective Spirocyclization with Ketimines as Substrates. Angewandte Chemie (International Ed. in English). PMID 27080309 DOI: 10.1002/Anie.201600453 |
0.772 |
|
| 2016 |
Ni H, Yao W, Lu Y. Enantioselective [3 + 2] annulation of α-substituted allenoates with β,γ-unsaturated N-sulfonylimines catalyzed by a bifunctional dipeptide phosphine. Beilstein Journal of Organic Chemistry. 12: 343-8. PMID 26977194 DOI: 10.3762/Bjoc.12.37 |
0.548 |
|
| 2016 |
Wen S, Li X, Yao W, Waheed A, Ullah N, Lu Y. Highly Enantioselective Conjugate Addition of Glycine Imines to Activated Alkenes Catalyzed by Amino-Acid-Derived Chiral Phosphonium Salts European Journal of Organic Chemistry. 2016: 4298-4301. DOI: 10.1002/Ejoc.201600794 |
0.553 |
|
| 2016 |
Wen S, Li X, Lu Y. Enantioselective Alkylation of Glycine Imine Promoted by Amino‐Acid‐Derived Phosphonium Salts Asian Journal of Organic Chemistry. 5: 1457-1460. DOI: 10.1002/Ajoc.201600394 |
0.617 |
|
| 2015 |
Wang T, Yu Z, Hoon DL, Huang KW, Lan Y, Lu Y. Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric γ-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings. Chemical Science. 6: 4912-4922. PMID 29142722 DOI: 10.1039/C5Sc01614B |
0.564 |
|
| 2015 |
Wang T, Yu Z, Hoon DL, Phee CY, Lan Y, Lu Y. Regiodivergent Enantioselective γ-Additions of Oxazolones to 2,3-Butadienoates Catalyzed by Phosphines: Synthesis of α,α-Disubstituted α-Amino Acids and N,O-Acetal Derivatives. Journal of the American Chemical Society. PMID 26629975 DOI: 10.1021/Jacs.5B10524 |
0.469 |
|
| 2015 |
Gandi VR, Lu Y. Phosphine-catalyzed regioselective Michael addition to allenoates. Chemical Communications (Cambridge, England). PMID 26392131 DOI: 10.1039/C5Cc06197K |
0.52 |
|
| 2015 |
Xu LW, Chen Y, Lu Y. Catalytic Silylations of Alcohols: Turning Simple Protecting-Group Strategies into Powerful Enantioselective Synthetic Methods. Angewandte Chemie (International Ed. in English). 54: 9456-66. PMID 26202094 DOI: 10.1002/Anie.201504127 |
0.395 |
|
| 2015 |
Wang T, Hoon DL, Lu Y. Enantioselective synthesis of 3-fluoro-3-allyl-oxindoles via phosphine-catalyzed asymmetric γ-addition of 3-fluoro-oxindoles to 2,3-butadienoates. Chemical Communications (Cambridge, England). 51: 10186-9. PMID 26013076 DOI: 10.1039/C5Cc03289J |
0.603 |
|
| 2015 |
Kwiatkowski J, Lu Y. Asymmetric Michael addition of α-fluoro-α-nitro esters to nitroolefins: towards synthesis of α-fluoro-α-substituted amino acids. Organic & Biomolecular Chemistry. 13: 2350-9. PMID 25563391 DOI: 10.1039/C4Ob02486A |
0.43 |
|
| 2015 |
Yao W, Dou X, Lu Y. Highly enantioselective synthesis of 3,4-dihydropyrans through a phosphine-catalyzed [4+2] annulation of allenones and β,γ-unsaturated α-keto esters. Journal of the American Chemical Society. 137: 54-7. PMID 25401753 DOI: 10.1021/Ja5109358 |
0.749 |
|
| 2015 |
Wang T, Yu Z, Hoon DL, Huang KW, Lan Y, Lu Y. Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric γ-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings Chemical Science. 6: 4912-4922. DOI: 10.1039/c5sc01614b |
0.309 |
|
| 2015 |
Zhou B, Ming So C, Lu Y, Hayashi T. A chiral bicyclo[2.2.2]octa-2,5-diene ligand substituted with the ferrocenyl group and its use for rhodium-catalyzed asymmetric 1,4-addition reactions Organic Chemistry Frontiers. 2: 127-132. DOI: 10.1039/C4Qo00292J |
0.568 |
|
| 2015 |
Gandi VR, Lu Y, Hayashi T. A chiral phosphine-olefin ligand derived from l-hydroxyproline and its use in the rhodium-catalyzed asymmetric 1,4-addition Tetrahedron Asymmetry. DOI: 10.1016/J.Tetasy.2015.05.004 |
0.668 |
|
| 2015 |
Zhang M, Xiao M, Wang S, Han D, Lu Y, Meng Y. Cerium oxide-based catalysts made by template-precipitation for the dimethyl carbonate synthesis from Carbon dioxide and methanol Journal of Cleaner Production. 103: 847-853. DOI: 10.1016/J.Jclepro.2014.09.024 |
0.472 |
|
| 2015 |
Zhou Y, Wang S, Xiao M, Han D, Lu Y, Meng Y. Formation of dimethyl carbonate on nature clay supported bimetallic copper-nickel catalysts Journal of Cleaner Production. 103: 925-933. DOI: 10.1016/J.Jclepro.2014.08.075 |
0.399 |
|
| 2015 |
Kwiatkowski J, Lu Y. Highly enantioselective Michael addition of 2-fluoro-1,3-diketones to nitroalkenes European Journal of Organic Chemistry. 2015: 320-324. DOI: 10.1002/Ejoc.201403361 |
0.589 |
|
| 2014 |
Dou X, Yao W, Jiang C, Lu Y. Enantioselective N-alkylation of isatins and synthesis of chiral N-alkylated indoles. Chemical Communications (Cambridge, England). 50: 11354-7. PMID 25163647 DOI: 10.1039/C4Cc04586F |
0.714 |
|
| 2014 |
Jiang C, Lu Y, Hayashi T. High performance of a palladium phosphinooxazoline catalyst in the asymmetric arylation of cyclic N-sulfonyl ketimines. Angewandte Chemie (International Ed. in English). 53: 9936-9. PMID 25044954 DOI: 10.1002/Anie.201406147 |
0.656 |
|
| 2014 |
Dou X, Yao W, Wen S, Lu Y. Facile regiospecific synthesis of 2,3-disubstituted indoles from isatins. Chemical Communications (Cambridge, England). 50: 9469-72. PMID 25011926 DOI: 10.1039/C4Cc04555F |
0.745 |
|
| 2014 |
Kwiatkowski J, Lu Y. Asymmetric Michael addition of α-fluoro-α-nitroalkanes to nitroolefins: facile preparation of fluorinated amines and tetrahydropyrimidines. Chemical Communications (Cambridge, England). 50: 9313-6. PMID 24999796 DOI: 10.1039/C4Cc03513E |
0.454 |
|
| 2014 |
Han X, Yao W, Wang T, Tan YR, Yan Z, Kwiatkowski J, Lu Y. Asymmetric synthesis of spiropyrazolones through phosphine-catalyzed [4+1] annulation. Angewandte Chemie (International Ed. in English). 53: 5643-7. PMID 24737675 DOI: 10.1002/Anie.201311214 |
0.63 |
|
| 2014 |
Wang T, Yao W, Zhong F, Pang GH, Lu Y. Phosphine-catalyzed enantioselective γ-addition of 3-substituted oxindoles to 2,3-butadienoates and 2-butynoates: use of prochiral nucleophiles. Angewandte Chemie (International Ed. in English). 53: 2964-8. PMID 24520067 DOI: 10.1002/Anie.201307757 |
0.819 |
|
| 2014 |
Shang JY, Li L, Lu Y, Yang KF, Xu LW. Enantioselective fluorination reaction of β-Ketoester-catalyzed chiral primary amine-based multifunctional catalyst systems Synthetic Communications. 44: 101-114. DOI: 10.1080/00397911.2013.791697 |
0.608 |
|
| 2014 |
Dou X, Yao W, Wen S, Lu Y. Synthesis of 2,3-Disubstituted Indoles from Isatins Synfacts. 10: 1189-1189. DOI: 10.1055/S-0034-1379341 |
0.509 |
|
| 2014 |
Yang W, Cui YM, Zhou W, Li L, Yang KF, Zheng ZJ, Lu Y, Xu LW. Enantioselective primary amine catalyzed aldol-type construction of trifluoromethylated tertiary alcohols Synlett. 25: 1461-1465. DOI: 10.1055/S-0033-1341281 |
0.606 |
|
| 2014 |
Kwiatkowski J, Lu Y. Highly enantioselective preparation of fluorinated phosphonates by michael addition of α-fluoro-β-ketophosphonates to nitroalkenes Asian Journal of Organic Chemistry. 3: 458-461. DOI: 10.1002/Ajoc.201300211 |
0.465 |
|
| 2013 |
Dou X, Zhou B, Yao W, Zhong F, Jiang C, Lu Y. A facile approach for the asymmetric synthesis of oxindoles with a 3-sulfenyl-substituted quaternary stereocenter. Organic Letters. 15: 4920-3. PMID 24067143 DOI: 10.1021/Ol402579X |
0.858 |
|
| 2013 |
Dou X, Yao W, Zhou B, Lu Y. Asymmetric synthesis of 3-spirocyclopropyl-2-oxindoles via intramolecular trapping of chiral aza-ortho-xylylene. Chemical Communications (Cambridge, England). 49: 9224-6. PMID 23995624 DOI: 10.1039/C3Cc45369C |
0.782 |
|
| 2013 |
Han X, Lee R, Chen T, Luo J, Lu Y, Huang KW. Kinetic evidence of an apparent negative activation enthalpy in an organocatalytic process. Scientific Reports. 3: 2557. PMID 23990028 DOI: 10.1038/Srep02557 |
0.418 |
|
| 2013 |
Dou X, Lu Y. Enantioselective conjugate addition of 3-fluoro-oxindoles to vinyl sulfone: an organocatalytic access to chiral 3-fluoro-3-substituted oxindoles. Organic & Biomolecular Chemistry. 11: 5217-21. PMID 23842569 DOI: 10.1039/C3Ob41267A |
0.807 |
|
| 2013 |
Lee R, Zhong F, Zheng B, Meng Y, Lu Y, Huang KW. The origin of enantioselectivity in the L-threonine-derived phosphine-sulfonamide catalyzed aza-Morita-Baylis-Hillman reaction: effects of the intramolecular hydrogen bonding. Organic & Biomolecular Chemistry. 11: 4818-24. PMID 23774825 DOI: 10.1039/C3Ob40144H |
0.79 |
|
| 2013 |
Luo J, Wang H, Zhong F, Kwiatkowski J, Xu LW, Lu Y. Highly diastereoselective and enantioselective direct Michael addition of phthalide derivatives to nitroolefins. Chemical Communications (Cambridge, England). 49: 5775-7. PMID 23689801 DOI: 10.1039/C3Cc42187B |
0.823 |
|
| 2013 |
Yang W, Jiang KZ, Lu X, Yang HM, Li L, Lu Y, Xu LW. Molecular assembly of an achiral phosphine and a chiral primary amine: a highly efficient supramolecular catalyst for the enantioselective Michael reaction of aldehydes with maleimides. Chemistry, An Asian Journal. 8: 1182-90. PMID 23554319 DOI: 10.1002/Asia.201300141 |
0.592 |
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| 2013 |
Zhong F, Dou X, Han X, Yao W, Zhu Q, Meng Y, Lu Y. Chiral phosphine catalyzed asymmetric Michael addition of oxindoles. Angewandte Chemie (International Ed. in English). 52: 943-7. PMID 23225504 DOI: 10.1002/Anie.201208285 |
0.845 |
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| 2013 |
Chen GY, Lu Y. Highly enantioselective Michael addition of α-substituted nitrophosphonates to a vinyl sulfone Synthesis (Germany). 45: 1654-1658. DOI: 10.1055/S-0033-1338434 |
0.519 |
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| 2013 |
Luo J, Jiang C, Wang H, Xu LW, Lu Y. Direct asymmetric Michael addition of phthalide derivatives to chalcones Tetrahedron Letters. 54: 5261-5265. DOI: 10.1016/J.Tetlet.2013.07.108 |
0.532 |
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| 2013 |
Zhong F, Jiang C, Yao W, Xu LW, Lu Y. Molecular sieve mediated decarboxylative Mannich and aldol reactions of β-ketoacids Tetrahedron Letters. 54: 4333-4336. DOI: 10.1016/J.Tetlet.2013.06.030 |
0.49 |
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| 2013 |
Luo J, Wu W, Xu LW, Meng Y, Lu Y. Enantioselective direct fluorination and chlorination of cyclic β-ketoesters mediated by phase-transfer catalysts Tetrahedron Letters. 54: 2623-2626. DOI: 10.1016/J.Tetlet.2013.03.028 |
0.509 |
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| 2013 |
Li F, Li L, Yang W, Zheng LS, Zheng ZJ, Jiang K, Lu Y, Xu LW. Chiral Ar-BINMOL-derived salan as fluorescent sensor for recognition of CuCl and cascade discrimination of α-amino acids Tetrahedron Letters. 54: 1584-1588. DOI: 10.1016/J.Tetlet.2013.01.047 |
0.36 |
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| 2013 |
Zhou YJ, Xiao M, Wang SJ, Han DM, Lu YX, Meng YZ. Effects of Mo promoters on the Cu-Fe bimetal catalysts for the DMC formation from CO2 and methanol Chinese Chemical Letters. 24: 307-310. DOI: 10.1016/J.Cclet.2013.02.001 |
0.335 |
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| 2012 |
Jiang C, Zhong F, Lu Y. Asymmetric organocatalytic decarboxylative Mannich reaction using β-keto acids: A new protocol for the synthesis of chiral β-amino ketones. Beilstein Journal of Organic Chemistry. 8: 1279-83. PMID 23019459 DOI: 10.3762/Bjoc.8.144 |
0.791 |
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| 2012 |
Dou X, Zhong F, Lu Y. A highly enantioselective synthesis of functionalized 2,3-dihydrofurans by a modified Feist-Bénary reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 13945-8. PMID 23008240 DOI: 10.1002/Chem.201202504 |
0.848 |
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| 2012 |
Chen GY, Zhong F, Lu Y. Asymmetric allylic alkylation of isatin-derived Morita-Baylis-Hillman carbonates with nitroalkanes. Organic Letters. 14: 3955-7. PMID 22830594 DOI: 10.1021/Ol301962E |
0.761 |
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| 2012 |
Zhong F, Yao W, Dou X, Lu Y. Enantioselective construction of 3-hydroxy oxindoles via decarboxylative addition of β-ketoacids to isatins. Organic Letters. 14: 4018-21. PMID 22830448 DOI: 10.1021/Ol301855W |
0.837 |
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| 2012 |
Zhong F, Chen GY, Han X, Yao W, Lu Y. Asymmetric construction of functionalized bicyclic imides via [3 + 2] annulation of MBH carbonates catalyzed by dipeptide-based phosphines. Organic Letters. 14: 3764-7. PMID 22789100 DOI: 10.1021/Ol301647G |
0.774 |
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| 2012 |
Dou X, Lu Y. Diastereodivergent synthesis of 3-spirocyclopropyl-2-oxindoles through direct enantioselective cyclopropanation of oxindoles. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 8315-9. PMID 22674465 DOI: 10.1002/Chem.201200655 |
0.763 |
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| 2012 |
Zhong F, Luo J, Chen GY, Dou X, Lu Y. Highly enantioselective regiodivergent allylic alkylations of MBH carbonates with phthalides. Journal of the American Chemical Society. 134: 10222-7. PMID 22621622 DOI: 10.1021/Ja303115M |
0.855 |
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| 2012 |
Luo J, Wang H, Zhong F, Kwiatkowski J, Xu LW, Lu Y. Direct asymmetric Mannich reaction of phthalides: facile access to chiral substituted isoquinolines and isoquinolinones. Chemical Communications (Cambridge, England). 48: 4707-9. PMID 22488217 DOI: 10.1039/C2Cc31439H |
0.837 |
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| 2012 |
Dou X, Han X, Lu Y. From the Feist-Bénary reaction to organocatalytic domino Michael-alkylation reactions: asymmetric synthesis of 3(2H)-furanones. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 85-9. PMID 22162312 DOI: 10.1002/Chem.201102796 |
0.74 |
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| 2012 |
Han X, Zhong F, Wang Y, Lu Y. Versatile enantioselective [3+2] cyclization between imines and allenoates catalyzed by dipeptide-based phosphines. Angewandte Chemie (International Ed. in English). 51: 767-70. PMID 22162303 DOI: 10.1002/Anie.201106672 |
0.817 |
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| 2012 |
Zhao Q, Han X, Wei Y, Shi M, Lu Y. Asymmetric [3+2] annulation of allenes with maleimides catalyzed by dipeptide-derived phosphines: facile creation of functionalized bicyclic cyclopentenes containing two tertiary stereogenic centers. Chemical Communications (Cambridge, England). 48: 970-2. PMID 22143407 DOI: 10.1039/C2Cc16904E |
0.565 |
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| 2012 |
Chen Y, Xiao M, Wang S, Han D, Lu Y, Meng Y. Porous diatomite-immobilized Cu-Ni bimetallic nanocatalysts for direct synthesis of dimethyl carbonate Journal of Nanomaterials. 2012. DOI: 10.1155/2012/610410 |
0.461 |
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| 2012 |
Zhong F, Han X, Wang Y, Lu Y. Highly enantioselective [4 + 2] annulations catalyzed by amino acid-based phosphines: Synthesis of functionalized cyclohexenes and 3-spirocyclohexene-2- oxindoles Chemical Science. 3: 1231-1234. DOI: 10.1039/C2Sc00963C |
0.553 |
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| 2012 |
Zhou Y, Wang S, Xiao M, Han D, Lu Y, Meng Y. Novel Cu-Fe bimetal catalyst for the formation of dimethyl carbonate from carbon dioxide and methanol Rsc Advances. 2: 6831-6837. DOI: 10.1039/C2Ra20359F |
0.344 |
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| 2012 |
Shen H, Lu X, Jiang KZ, Yang KF, Lu Y, Zheng ZJ, Lai GQ, Xu LW. Dimethylbut-2-ynedioate mediated esterification of acids via sp 3 C-N bond cleavage of benzylic tertiary amines Tetrahedron. 68: 8916-8923. DOI: 10.1016/J.Tet.2012.08.024 |
0.45 |
|
| 2011 |
Chen GY, Zhong F, Lu Y. Highly enantioselective and regioselective substitution of Morita-Baylis-Hillman carbonates with nitroalkanes. Organic Letters. 13: 6070-3. PMID 22035214 DOI: 10.1021/Ol202555V |
0.81 |
|
| 2011 |
Liu C, Dou X, Lu Y. Organocatalytic asymmetric aldol reaction of hydroxyacetone with β,γ-unsaturated α-keto esters: facile access to chiral tertiary alcohols. Organic Letters. 13: 5248-51. PMID 21902199 DOI: 10.1021/Ol2021274 |
0.784 |
|
| 2011 |
Han X, Wang Y, Zhong F, Lu Y. Enantioselective Morita-Baylis-Hillman reaction promoted by L-threonine-derived phosphine-thiourea catalysts. Organic & Biomolecular Chemistry. 9: 6734-40. PMID 21858321 DOI: 10.1039/C1Ob05881A |
0.802 |
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| 2011 |
Zhong F, Han X, Wang Y, Lu Y. Highly enantioselective [3+2] annulation of Morita-Baylis-Hillman adducts mediated by L-threonine-derived phosphines: synthesis of 3-spirocyclopentene-2-oxindoles having two contiguous quaternary centers. Angewandte Chemie (International Ed. in English). 50: 7837-41. PMID 21728218 DOI: 10.1002/Anie.201102094 |
0.767 |
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| 2011 |
Liu C, Zhu Q, Huang KW, Lu Y. Primary amine/CSA ion pair: a powerful catalytic system for the asymmetric enamine catalysis. Organic Letters. 13: 2638-41. PMID 21510614 DOI: 10.1021/Ol200747X |
0.604 |
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| 2011 |
Zhong F, Wang Y, Han X, Huang KW, Lu Y. L-threonine-derived novel bifunctional phosphine-sulfonamide catalyst-promoted enantioselective aza-Morita-Baylis-Hillman reaction. Organic Letters. 13: 1310-3. PMID 21332151 DOI: 10.1021/Ol103145G |
0.806 |
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| 2011 |
Luo J, Wang H, Han X, Xu LW, Kwiatkowski J, Huang KW, Lu Y. The direct asymmetric vinylogous aldol reaction of furanones with α-ketoesters: access to chiral γ-butenolides and glycerol derivatives. Angewandte Chemie (International Ed. in English). 50: 1861-4. PMID 21328657 DOI: 10.1002/Anie.201006316 |
0.557 |
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| 2011 |
Han X, Wang Y, Zhong F, Lu Y. Enantioselective [3 + 2] cycloaddition of allenes to acrylates catalyzed by dipeptide-derived phosphines: facile creation of functionalized cyclopentenes containing quaternary stereogenic centers. Journal of the American Chemical Society. 133: 1726-9. PMID 21226456 DOI: 10.1021/Ja1106282 |
0.806 |
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| 2011 |
Zhong F, Chen GY, Lu Y. Enantioselective Morita-Baylis-Hillman reaction of isatins with acrylates: facile creation of 3-hydroxy-2-oxindoles. Organic Letters. 13: 82-5. PMID 21138329 DOI: 10.1021/Ol102597S |
0.8 |
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| 2011 |
Shetty RS, Lee Y, Liu B, Husain A, Joseph RW, Lu Y, Nelson D, Mihelcic J, Chao W, Moffett KK, Schumacher A, Flubacher D, Stojanovic A, Bukhtiyarova M, Williams K, et al. Synthesis and pharmacological evaluation of N-(3-(1H-indol-4-yl)-5-(2-methoxyisonicotinoyl)phenyl)methanesulfonamide (LP-261), a potent antimitotic agent. Journal of Medicinal Chemistry. 54: 179-200. PMID 21126027 DOI: 10.1021/Jm100659V |
0.305 |
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| 2011 |
Wang SX, Han X, Zhong F, Wang Y, Lu Y. Novel amino acid based bifunctional chiral phosphines Synlett. 2766-2778. DOI: 10.1055/S-0031-1289538 |
0.604 |
|
| 2011 |
Zhong F, Han X, Wang Y, Lu Y. [3+2] Annulation of MBH AdductsPromoted by Bifunctional Phosphines Synfacts. 2011: 1020-1020. DOI: 10.1055/S-0030-1260921 |
0.515 |
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| 2011 |
Han X, Wang SX, Zhong F, Lu Y. Formation of functionalized cyclopentenes via catalytic asymmetric [3+2] cycloaddition of acrylamides with an allenoate promoted by dipeptide-derived phosphines Synthesis. 1859-1864. DOI: 10.1055/S-0030-1260460 |
0.604 |
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| 2011 |
Zhong F, Wang Y, Han X, Huang K-, Lu Y. A Novel Bifunctional Phosphine Catalyst for Aza-Morita-Baylis-HillmanReactions Synfacts. 2011: 551-551. DOI: 10.1055/S-0030-1259857 |
0.454 |
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| 2011 |
Han X, Wang Y, Zhong F, Lu Y. Dipeptide-Based Phosphine Catalyst for Cycloaddition of Allenesto Acrylates Synfacts. 2011: 442-442. DOI: 10.1055/S-0030-1259612 |
0.455 |
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| 2011 |
Shi ZH, Sheng H, Yang KF, Jiang JX, Lai GQ, Lu Y, Xu LW. Diarylprolinol silyl ether catalyzed asymmetric friedel-crafts alkylation of indoles with α,β-unsaturated aldehydes: Enhanced enantioselectivity and mechanistic investigations European Journal of Organic Chemistry. 66-70. DOI: 10.1002/Ejoc.201001404 |
0.528 |
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| 2011 |
Wang H, Luo J, Han X, Lu Y. Enantioselective synthesis of chromanones via a tryptophan-derived bifunctional thiourea-catalyzed oxa-Michael-Michael cascade reaction Advanced Synthesis and Catalysis. 353: 2971-2975. DOI: 10.1002/Adsc.201100419 |
0.655 |
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| 2010 |
Liu X, Lu Y. Asymmetric synthesis of 2-aryl-2,3-dihydro-4-quinolones via bifunctional thiourea-mediated intramolecular cyclization. Organic Letters. 12: 5592-5. PMID 21047098 DOI: 10.1021/Ol102519Z |
0.583 |
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| 2010 |
Zhu Q, Lu Y. Stereocontrolled creation of all-carbon quaternary stereocenters by organocatalytic conjugate addition of oxindoles to vinyl sulfone. Angewandte Chemie (International Ed. in English). 49: 7753-6. PMID 20821787 DOI: 10.1002/Anie.201003837 |
0.358 |
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| 2010 |
Zhu Q, Lu Y. Facile synthesis of bicyclic amidines and imidazolines from 1,2-diamines. Organic Letters. 12: 4156-9. PMID 20726557 DOI: 10.1021/Ol101747N |
0.569 |
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| 2010 |
Liu X, Lu Y. Bifunctional thiourea-promoted cascade aza-Michael-Henry-dehydration reactions: asymmetric preparation of 3-nitro-1,2-dihydroquinolines. Organic & Biomolecular Chemistry. 8: 4063-5. PMID 20648391 DOI: 10.1039/C0Ob00223B |
0.643 |
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| 2010 |
Liu C, Lu Y. Primary amine/(+)-CSA salt-promoted organocatalytic conjugate addition of nitro esters to enones. Organic Letters. 12: 2278-81. PMID 20411973 DOI: 10.1021/ol1006407 |
0.432 |
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| 2010 |
Zhu Q, Lu Y. Chiral primary amine mediated conjugate addition of branched aldehydes to vinyl sulfone: asymmetric generation of quaternary carbon centers. Chemical Communications (Cambridge, England). 46: 2235-7. PMID 20234917 DOI: 10.1039/B919549A |
0.538 |
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| 2010 |
Jiang Z, Yang H, Han X, Luo J, Wong MW, Lu Y. Direct asymmetric aldol reactions between aldehydes and ketones catalyzed by L-tryptophan in the presence of water. Organic & Biomolecular Chemistry. 8: 1368-77. PMID 20204209 DOI: 10.1039/B921460G |
0.524 |
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| 2010 |
Jiang ZY, Wu JR, Li L, Chen XH, Lai GQ, Jiang JX, Lu Y, Xu LW. Efficient Lewis acid-assisted Brønsted acid (LBA) catalysis in the iron-catalyzed Friedel-Crafts alkylation reaction of indoles Central European Journal of Chemistry. 8: 669-673. DOI: 10.2478/S11532-010-0016-0 |
0.438 |
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| 2010 |
Jiang Z, Lu Y. Direct asymmetric aldol reaction of acetone with α-ketoesters catalyzed by primary-tertiary diamine organocatalysts Tetrahedron Letters. 51: 1884-1886. DOI: 10.1016/J.Tetlet.2010.02.044 |
0.562 |
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| 2010 |
Han X, Zhong F, Lu Y. Highly enantioselective amination reactions of fluorinated keto esters catalyzed by novel chiral guanidines derived from cinchona alkaloids Advanced Synthesis and Catalysis. 352: 2778-2782. DOI: 10.1002/Adsc.201000562 |
0.644 |
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| 2009 |
Han X, Kwiatkowski J, Xue F, Huang KW, Lu Y. Asymmetric Mannich reaction of fluorinated ketoesters with a tryptophan-derived bifunctional thiourea catalyst. Angewandte Chemie (International Ed. in English). 48: 7604-7. PMID 19739170 DOI: 10.1002/Anie.200903635 |
0.602 |
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| 2009 |
Han X, Luo J, Liu C, Lu Y. Asymmetric generation of fluorine-containing quaternary carbons adjacent to tertiary stereocenters: uses of fluorinated methines as nucleophiles. Chemical Communications (Cambridge, England). 2044-6. PMID 19333485 DOI: 10.1039/B823184B |
0.622 |
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| 2009 |
Xu LW, Luo J, Lu Y. Asymmetric catalysis with chiral primary amine-based organocatalysts. Chemical Communications (Cambridge, England). 1807-21. PMID 19319412 DOI: 10.1039/B821070E |
0.583 |
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| 2009 |
Zhu Q, Lu Y. Enantioselective conjugate addition of nitroalkanes to vinyl sulfone: an organocatalytic access to chiral amines. Organic Letters. 11: 1721-4. PMID 19317479 DOI: 10.1021/Ol9003349 |
0.603 |
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| 2009 |
Luo J, Xu LW, Hay RA, Lu Y. Asymmetric Michael addition mediated by novel cinchona alkaloid-derived bifunctional catalysts containing sulfonamides. Organic Letters. 11: 437-40. PMID 19072133 DOI: 10.1021/Ol802486M |
0.555 |
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| 2009 |
Zhu Q, Lu Y. Chiral amine-mediated asymmetric conjugate additions to vinyl sulfones Australian Journal of Chemistry. 62: 951-955. DOI: 10.1071/Ch09137 |
0.512 |
|
| 2009 |
Han X, Luo J, Liu C, Lu Y. Asymmetric Generation of Fluorine Containing Quaternary CarbonCenters Synfacts. 2009: 564-564. DOI: 10.1055/S-0029-1216582 |
0.382 |
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| 2009 |
Luo J, Xu L-, Hay RAS, Lu Y. Bifunctional Cinchona Sulfonamides in Asymmetric MichaelReaction Synfacts. 2009: 331-331. DOI: 10.1055/S-0028-1087730 |
0.543 |
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| 2009 |
Ju Y, Xu L, Li L, Lai G, Qiu H, Jiang J, Lu Y. Erratum to “Noyori’s Ts-DPEN ligand: an efficient bifunctional primary amine-based organocatalyst in enantio- and diastereoselective Michael addition of 1,3-dicarbonyl indane compounds to nitroolefins” [Tetrahedron Lett. 49 (2008) 6773] Tetrahedron Letters. 50: 135. DOI: 10.1016/J.Tetlet.2008.10.123 |
0.382 |
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| 2009 |
Bian J, Xiao M, Wang S, Wang X, Lu Y, Meng Y. Highly effective synthesis of dimethyl carbonate from methanol and carbon dioxide using a novel copper-nickel/graphite bimetallic nanocomposite catalyst Chemical Engineering Journal. 147: 287-296. DOI: 10.1016/J.Cej.2008.11.006 |
0.401 |
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| 2009 |
Bian J, Xiao M, Wang SJ, Lu YX, Meng YZ. Graphite oxide as a novel host material of catalytically active Cu-Ni bimetallic nanoparticles Catalysis Communications. 10: 1529-1533. DOI: 10.1016/j.catcom.2009.04.009 |
0.331 |
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| 2009 |
Bian J, Xiao M, Wang S, Lu Y, Meng Y. Direct synthesis of DMC from CH3OH and CO2 over V-doped Cu-Ni/AC catalysts Catalysis Communications. 10: 1142-1145. DOI: 10.1016/J.Catcom.2008.12.008 |
0.407 |
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| 2009 |
Bian J, Xiao M, Wang SJ, Lu YX, Meng YZ. Carbon nanotubes supported Cu-Ni bimetallic catalysts and their properties for the direct synthesis of dimethyl carbonate from methanol and carbon dioxide Applied Surface Science. 255: 7188-7196. DOI: 10.1016/J.Apsusc.2009.03.057 |
0.373 |
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| 2008 |
Zhu Q, Cheng L, Lu Y. Asymmetric organocatalytic Michael addition of ketones to vinyl sulfone. Chemical Communications (Cambridge, England). 6315-7. PMID 19048140 DOI: 10.1039/B816307C |
0.593 |
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| 2008 |
Zhu Q, Lu Y. Organocatalytic Michael addition of aldehydes to vinyl sulfones: enantioselective alpha-alkylations of aldehydes and their derivatives. Organic Letters. 10: 4803-6. PMID 18834133 DOI: 10.1021/ol8019296 |
0.46 |
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| 2008 |
Ghosh A, Luo J, Liu C, Weltrowska G, Lemieux C, Chung NN, Lu Y, Schiller PW. Novel opioid peptide derived antagonists containing (2S)-2-methyl-3-(2,6-dimethyl-4-carbamoylphenyl)propanoic acid [(2S)-Mdcp]. Journal of Medicinal Chemistry. 51: 5866-70. PMID 18800771 DOI: 10.1021/Jm8004702 |
0.306 |
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| 2008 |
Xu LW, Lu Y. Primary amino acids: privileged catalysts in enantioselective organocatalysis. Organic & Biomolecular Chemistry. 6: 2047-53. PMID 18528563 DOI: 10.1039/B803116A |
0.559 |
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| 2008 |
Ju Y, Xu L, Li L, Lai G, Qiu H, Jiang J, Lu Y. Noyori’s Ts-DPEN ligand: an efficient bifunctional primary amine-based organocatalyst in enantio- and diastereoselective Michael addition of 1,3-dicarbonyl indane compounds to nitroolefins Tetrahedron Letters. 49: 6773-6777. DOI: 10.1016/J.Tetlet.2008.09.025 |
0.494 |
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| 2007 |
Cheng L, Han X, Huang H, Wong MW, Lu Y. Highly diastereoselective and enantioselective direct organocatalytic anti-selective Mannich reactions employing N-tosylimines. Chemical Communications (Cambridge, England). 4143-5. PMID 17925956 DOI: 10.1039/B706793C |
0.536 |
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| 2007 |
Cheng L, Wu X, Lu Y. Direct asymmetric three-component organocatalytic anti-selective Mannich reactions in a purely aqueous system. Organic & Biomolecular Chemistry. 5: 1018-20. PMID 17377652 DOI: 10.1039/B701579H |
0.533 |
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| 2007 |
Cheng L, Aw C, Ong SS, Lu Y. Facile cleavage of ethers in ionic liquid Bulletin of the Chemical Society of Japan. 80: 2008-2010. DOI: 10.1246/Bcsj.80.2008 |
0.382 |
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| 2007 |
Wu X, Jiang Z, Shen H, Lu Y. Highly Efficient Threonine-Derived Organocatalysts for Direct Asymmetric Aldol Reactions in Water Advanced Synthesis & Catalysis. 349: 812-816. DOI: 10.1002/Adsc.200600564 |
0.514 |
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| 2006 |
Jiang Z, Liang Z, Wu X, Lu Y. Asymmetric aldol reactions catalyzed by tryptophan in water. Chemical Communications (Cambridge, England). 2801-3. PMID 17009468 DOI: 10.1039/B606154K |
0.497 |
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| 2006 |
Lu Y. Recent advances in the stereocontrolled synthesis of antisense phosphorothioates. Mini Reviews in Medicinal Chemistry. 6: 319-30. PMID 16515471 DOI: 10.2174/138955706776073439 |
0.302 |
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| 2006 |
Jiang Z, Liang Z, Wu X, Lu Y. l-Tryptophan-Catalyzed Aldol Reaction in Water Synfacts. 2006: 842-842. DOI: 10.1055/S-2006-942030 |
0.395 |
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| 2006 |
Cao M, Meng Y, Lu Y. Synthesis of dimethyl carbonate (dmc) from co2, ethylene oxide and methanol using heterogeneous anion exchange resins as catalysts Reaction Kinetics and Catalysis Letters. 88: 251-259. DOI: 10.1007/S11144-006-0059-6 |
0.497 |
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| 2005 |
Cao M, Meng Y, Lu Y. Synthesis of diphenyl carbonate from dimethyl carbonate and phenol using O2-promoted PbO/MgO catalysts Catalysis Communications. 6: 802-807. DOI: 10.1016/J.Catcom.2005.07.020 |
0.447 |
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| 2001 |
Lu Y, Nguyen TM-, Weltrowska G, Berezowska I, Lemieux C, Chung NN, Schiller PW. [2', 6'-dimethyltyrosine]dynorphin A(1-11)-NH2 analogues lacking an N-terminal amino group : Potent and selective κ opioid antagonists Journal of Medicinal Chemistry. 44: 3048-3053. PMID 11543672 DOI: 10.1021/Jm0101186 |
0.302 |
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| 2001 |
Lu Y, Weltrowska G, Lemieux C, Chung NN, Schiller PW. Stereospecific synthesis of (2S)-2-methyl-3-(2′,6′-dimethyl-4′-hydroxyphenyl)-propionic acid (Mdp) and its incorporation into an opioid peptide Bioorganic & Medicinal Chemistry Letters. 11: 323-325. PMID 11212101 DOI: 10.1016/S0960-894X(00)00660-0 |
0.32 |
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| 2001 |
Lu Y, Schiller PW. Stereospecific Syntheses of 2-Alkyl and 2-Phenyl Substituted 3-(2,6-Dimethyl-4-hydroxyphenyl)propanoic Acids Synthesis. 2001: 1639-1644. DOI: 10.1055/S-2001-16757 |
0.44 |
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| 2001 |
Lu Y, Just G. Stereoselective synthesis of dithymidine phosphorothioates using D-xylose derived chiral auxiliaries Tetrahedron. 57: 1677-1687. DOI: 10.1016/S0040-4020(00)01170-4 |
0.701 |
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| 2000 |
Lu Y, Just G. Stereoselective Synthesis of R(P)- and S(P)-Dithymidine Phosphorothioates via Chiral Indolooxazaphosphorine Intermediates Derived from Tryptophan This work was financially supported by Natural Science and Engineering Research Council of Canada (NSERC). We thank Nadim Saadeh and Dr. Orval Mamer, McGill University biomedical mass spectroscopy unit, for recording mass spectra. Angewandte Chemie (International Ed. in English). 39: 4521-4524. PMID 11169657 DOI: 10.1002/1521-3773(20001215)39:24<4521::Aid-Anie4521>3.0.Co;2-M |
0.536 |
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| 2000 |
Manoharan M, Lu Y, Casper MD, Just G. Allyl group as a protecting group for internucleotide phosphate and thiophosphate linkages in oligonucleotide synthesis: facile oxidation and deprotection conditions. Organic Letters. 2: 243-6. PMID 10814292 |
0.55 |
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| 2000 |
Lu Y, Just G. Study on the diastereoselective synthesis of dithymidine phosphorothioates through a D-xylose derived chiral auxiliary and development of a novel catalyst Tetrahedron Letters. 41: 9223-9227. DOI: 10.1016/S0040-4039(00)01678-6 |
0.663 |
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| 2000 |
Lu Y, Just G. Stereoselective synthesis of phosphorothioate and alkylphosphinate analogs using a L-tryptophan derived chiral auxiliary Tetrahedron. 56: 4355-4365. DOI: 10.1016/S0040-4020(00)00308-2 |
0.664 |
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