| Year |
Citation |
Score |
| 2023 |
Leung VM, Pook CM, Chan TC, Yeung YY. Trialkylphosphonium Oxoborate as C(sp3)-H Oxyanion Hole Catalyst for Diels-Alder Reaction. Chemistry, An Asian Journal. e202300981. PMID 38116878 DOI: 10.1002/asia.202300981 |
0.48 |
|
| 2023 |
Leung VM, Wong HF, Pook CM, Tse YS, Yeung YY. Trialkylphosphonium oxoborates as C(sp)-H oxyanion holes and their application in catalytic chemoselective acetalization. Chemical Science. 14: 12684-12692. PMID 38020391 DOI: 10.1039/d3sc03081d |
0.371 |
|
| 2023 |
Pan L, Lee KM, Chan YY, Ke Z, Yeung YY. Applications of the DIB-BBr Protocol in Bromination Reactions. Organic Letters. 25: 53-57. PMID 36594727 DOI: 10.1021/acs.orglett.2c03777 |
0.588 |
|
| 2022 |
Pan L, Zheng L, Chen Y, Ke Z, Yeung YY. Mechanochemical and Catalyst-Free Cascade Synthesis of 1,3-Diols and 1,4-Iodoalcohols Using Styrenes and Hypervalent Iodine Reagents. Angewandte Chemie (International Ed. in English). PMID 35829718 DOI: 10.1002/anie.202207926 |
0.694 |
|
| 2022 |
Zhang Q, Chan YY, Zhang M, Yeung YY, Ke Z. Hypervalent Chalcogenonium⋅⋅⋅π Bonding Catalysis. Angewandte Chemie (International Ed. in English). e202208009. PMID 35792421 DOI: 10.1002/anie.202208009 |
0.531 |
|
| 2021 |
Wong J, Yeung YY. Solvent and catalyst-free bromofunctionalization of olefins using a mechanochemical approach. Rsc Advances. 11: 13564-13570. PMID 35423890 DOI: 10.1039/d1ra01816g |
0.437 |
|
| 2021 |
Hu RB, Qiang S, Chan YY, Huang J, Xu T, Yeung YY. Access to Bromo-γ-butenolides via Zwitterion-Catalyzed Rearrangement of Cyclopropene Carboxylic Acids. Organic Letters. PMID 34854693 DOI: 10.1021/acs.orglett.1c03751 |
0.442 |
|
| 2021 |
Pan L, Ke Z, Yeung YY. Lewis Base Catalyzed Dioxygenation of Olefins with Hypervalent Iodine Reagents. Organic Letters. PMID 34632779 DOI: 10.1021/acs.orglett.1c02872 |
0.662 |
|
| 2021 |
Chan YC, Wang X, Lam YP, Wong J, Tse YS, Yeung YY. A Catalyst-Controlled Enantiodivergent Bromolactonization. Journal of the American Chemical Society. PMID 34350758 DOI: 10.1021/jacs.1c05680 |
0.471 |
|
| 2021 |
Jiang X, Xu X, Xu W, Yu P, Yeung YY. Catalytic Enantioselective Halocyclizations to Access Benzoxazepinones and Benzoxazecinones. Organic Letters. PMID 34342993 DOI: 10.1021/acs.orglett.1c02117 |
0.445 |
|
| 2021 |
Xiong X, Wong J, Yeung YY. Silver Salt-Mediated Allylation Reactions Using Allyl Bromides. The Journal of Organic Chemistry. PMID 33861601 DOI: 10.1021/acs.joc.1c00480 |
0.781 |
|
| 2020 |
Gieuw MH, Chen S, Ke Z, Houk KN, Yeung YY. Boron tribromide as a reagent for anti-Markovnikov addition of HBr to cyclopropanes. Chemical Science. 11: 9426-9433. PMID 34094209 DOI: 10.1039/d0sc02567d |
0.556 |
|
| 2020 |
Lam YP, Lam Z, Yeung YY. Zwitterion-Catalyzed Isomerization of Maleic to Fumaric Acid Diesters. The Journal of Organic Chemistry. PMID 33315398 DOI: 10.1021/acs.joc.0c02316 |
0.317 |
|
| 2020 |
Ke Z, Lam YP, Chan KS, Yeung YY. Zwitterion-Catalyzed Deacylative Dihalogenation of β-Oxo Amides. Organic Letters. PMID 32870014 DOI: 10.1021/Acs.Orglett.0C02701 |
0.685 |
|
| 2020 |
Ng WH, Hu RB, Lam YP, Yeung YY. Zwitterion-Catalyzed Intermolecular Bromoesterifications. Organic Letters. PMID 32639749 DOI: 10.1021/Acs.Orglett.0C01928 |
0.372 |
|
| 2020 |
Gieuw MH, Chen S, Ke Z, Houk KN, Yeung Y. Boron tribromide as a reagent for anti-Markovnikov addition of HBr to cyclopropanes Chemical Science. 11: 9426-9433. DOI: 10.1039/D0Sc02567D |
0.54 |
|
| 2020 |
Wong J, Ke Z, Yeung Y. Lipophilic indole mediated chemoselective α-monobromination of 1,3-dicarbonyl compounds Tetrahedron Letters. 61: 151772. DOI: 10.1016/J.Tetlet.2020.151772 |
0.674 |
|
| 2020 |
Xiong X, Zheng T, Wang X, Tse YS, Yeung Y. Access to Chiral Bisphenol Ligands (BPOL) through Desymmetrizing Asymmetric Ortho-Selective Halogenation Chem. 6: 919-932. DOI: 10.1016/J.Chempr.2020.01.009 |
0.783 |
|
| 2020 |
Leung VM, Gieuw MH, Ke Z, Yeung Y. Intermolecular Electrophilic Bromoesterification and Bromoetherification of Unactivated Cyclopropanes Advanced Synthesis & Catalysis. 362: 2039-2044. DOI: 10.1002/Adsc.201901665 |
0.657 |
|
| 2019 |
Chan YC, Yeung YY. Halogen-Bond-Catalyzed Addition of Carbon-Based Nucleophiles to N-Acylimminium Ions. Organic Letters. PMID 31282678 DOI: 10.1021/Acs.Orglett.9B02006 |
0.472 |
|
| 2019 |
Shi Y, Wong J, Ke Z, Yeung YY. Lipophilic Indole-Catalyzed Intermolecular Bromoesterification of Olefins in Nonpolar Media. The Journal of Organic Chemistry. PMID 30816048 DOI: 10.1021/Acs.Joc.9B00029 |
0.722 |
|
| 2019 |
Lam Y, Wang X, Tan F, Ng W, Tse YS, Yeung Y. Amide/Iminium Zwitterionic Catalysts for (Trans)esterification: Application in Biodiesel Synthesis Acs Catalysis. 9: 8083-8092. DOI: 10.1021/Acscatal.9B01959 |
0.555 |
|
| 2019 |
Ke Z, Yeung Y. Unearthing the Mechanism of Umpolung Amide Synthesis Chem. 5: 1014-1016. DOI: 10.1016/J.Chempr.2019.04.014 |
0.631 |
|
| 2019 |
Wang H, Wang Y, Liu S, Mai Y, Zong X, Gao H, Hu R, Jiang X, Yeung Y. Enantioselective Fluorocyclizations Mediated by Amino‐Acid‐Derived Phthalazine Advanced Synthesis & Catalysis. 361: 5334-5339. DOI: 10.1002/Adsc.201900814 |
0.441 |
|
| 2018 |
He X, Wang X, Tse YS, Ke Z, Yeung YY. Applications of Selenonium Cation as a Lewis Acid in Organocatalytic Reactions. Angewandte Chemie (International Ed. in English). PMID 30084241 DOI: 10.1002/Anie.201806965 |
0.659 |
|
| 2018 |
Jiang X, Liu S, Yang S, Jing M, Xu L, Yu P, Wang Y, Yeung YY. Enantioselective Bromolactonization of Deactivated Olefinic Acids. Organic Letters. PMID 29750534 DOI: 10.1021/Acs.Orglett.8B01125 |
0.516 |
|
| 2018 |
Lam YP, Yeung YY. Metal-free Allylic Oxidation of Steroids Using TBAI/TBHP Organocatalytic Protocol. Chemistry, An Asian Journal. PMID 29569349 DOI: 10.1002/Asia.201800256 |
0.335 |
|
| 2018 |
Gieuw MH, Ke Z, Yeung YY. Lewis Base-Promoted Ring-Opening 1,3-Dioxygenation of Unactivated Cyclopropanes using Hypervalent Iodine Reagent. Angewandte Chemie (International Ed. in English). PMID 29431266 DOI: 10.1002/Anie.201713422 |
0.612 |
|
| 2018 |
Chan YC, Yeung YY. Halogen-Bond Catalyzed Bromocarbocyclization. Angewandte Chemie (International Ed. in English). PMID 29424047 DOI: 10.1002/Anie.201800261 |
0.408 |
|
| 2018 |
Shi Y, Ke Z, Yeung Y. Environmentally benign indole-catalyzed position-selective halogenation of thioarenes and other aromatics Green Chemistry. 20: 4448-4452. DOI: 10.1039/C8Gc02415D |
0.599 |
|
| 2018 |
Xiong X, Yeung Y. Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications Acs Catalysis. 8: 4033-4043. DOI: 10.1021/Acscatal.8B00327 |
0.806 |
|
| 2018 |
See JY, Yang H, Zhao Y, Wong MW, Ke Z, Yeung Y. Desymmetrizing Enantio- and Diastereoselective Selenoetherification through Supramolecular Catalysis Acs Catalysis. 8: 850-858. DOI: 10.1021/Acscatal.7B03510 |
0.724 |
|
| 2018 |
Jiang X, Wang H, He H, Wang W, Wang Y, Ke Z, Yeung Y. Enantioseletive Fluorination of 3-Functionalized Oxindoles Using Electron-rich Amino Urea Catalyst Advanced Synthesis & Catalysis. 360: 4710-4714. DOI: 10.1002/Adsc.201801133 |
0.623 |
|
| 2018 |
Gieuw MH, Leung VM, Ke Z, Yeung Y. Electrophilic Bromolactonization of Cyclopropyl Diesters Using Lewis Basic Chalcogenide Catalysts Advanced Synthesis & Catalysis. 360: 4306-4311. DOI: 10.1002/Adsc.201800886 |
0.657 |
|
| 2018 |
Ke Z, Chen T, Yeung Y, Han Z, Ding K. Indole‐Catalyzed Bromolactonization: Preparation of Bromolactone in Lipophilic Media Organic Syntheses. 95: 256-266. DOI: 10.1002/0471264229.Os095.18 |
0.532 |
|
| 2017 |
Xiong X, Tan F, Yeung YY. Zwitterionic-Salt-Catalyzed Site-Selective Monobromination of Arenes. Organic Letters. PMID 28782957 DOI: 10.1021/Acs.Orglett.7B01899 |
0.8 |
|
| 2017 |
Liu Y, Yeung YY. Ring strain-dictated divergent fluorinating Prins cyclization or semipinacol rearrangement. Organic & Biomolecular Chemistry. PMID 28749510 DOI: 10.1039/C7Ob01567D |
0.428 |
|
| 2017 |
Liu Y, Yeung YY. Synthesis of Macrocyclic Ketones through Catalyst-Free Electrophilic Halogen-Mediated Semipinacol Rearrangement: Application to the Total Synthesis of (±)-Muscone. Organic Letters. PMID 28244759 DOI: 10.1021/Acs.Orglett.7B00350 |
0.459 |
|
| 2017 |
Liu Y, Tse YS, Kwong FY, Yeung Y. Accessing Axially Chiral Biaryls via Organocatalytic Enantioselective Dynamic-Kinetic Resolution-Semipinacol Rearrangement Acs Catalysis. 7: 4435-4440. DOI: 10.1021/Acscatal.7B01056 |
0.416 |
|
| 2017 |
Yu WZ, Cheng YA, Wong MW, Yeung Y. Atmosphere- and Temperature-Controlled Regioselective Aminobromination of Olefins Advanced Synthesis & Catalysis. 359: 234-239. DOI: 10.1002/Adsc.201600821 |
0.435 |
|
| 2016 |
Xiong X, Yeung YY. Highly ortho-Selective Chlorination of Anilines Using a Secondary Ammonium Salt Organocatalyst. Angewandte Chemie (International Ed. in English). PMID 27900807 DOI: 10.1002/Anie.201607388 |
0.803 |
|
| 2016 |
Gieuw MH, Ke Z, Yeung YY. Lewis Base Catalyzed Stereo- and Regioselective Bromocyclization. Chemical Record (New York, N.Y.). PMID 27701807 DOI: 10.1002/Tcr.201600088 |
0.692 |
|
| 2016 |
Chen T, Yeung YY. Trifluoroacetic acid catalyzed highly regioselective bromocyclization of styrene-type carboxylic acid. Organic & Biomolecular Chemistry. PMID 27126404 DOI: 10.1039/C6Ob00756B |
0.392 |
|
| 2016 |
Wong YC, Yeung YY. A convenient method for the synthesis of α-carboxylate ester bromolactones via bromolactonization of alkenoic diesters. Organic & Biomolecular Chemistry. PMID 26932838 DOI: 10.1039/C6Ob00311G |
0.501 |
|
| 2016 |
Ke Z, Tan CK, Liu Y, Lee KGZ, Yeung YY. Catalytic and enantioselective bromoetherification of olefinic 1,3-diols: Mechanistic insight Tetrahedron. 72: 2683-2689. DOI: 10.1016/J.Tet.2015.09.016 |
0.697 |
|
| 2016 |
Ke Z, Wong YC, See JY, Yeung YY. Electrophilic Bromolactonization of Cyclopropyl Carboxylic Acids Using Lewis Basic Sulfide Catalyst Advanced Synthesis and Catalysis. 358: 1719-1724. DOI: 10.1002/Adsc.201500999 |
0.699 |
|
| 2015 |
Cheng YA, Yu WZ, Yeung YY. An Unexpected Bromolactamization of Olefinic Amides Using a Three-Component Co-catalyst System. The Journal of Organic Chemistry. PMID 26679219 DOI: 10.1021/Acs.Joc.5B02390 |
0.504 |
|
| 2015 |
Wong YC, Ke Z, Yeung YY. Lewis Basic Sulfide Catalyzed Electrophilic Bromocyclization of Cyclopropylmethyl Amide. Organic Letters. 17: 4944-7. PMID 26439814 DOI: 10.1021/Acs.Orglett.5B02557 |
0.718 |
|
| 2015 |
Cheng YA, Yu WZ, Yeung YY. Carbamate-catalyzed enantioselective bromolactamization. Angewandte Chemie (International Ed. in English). 54: 12102-6. PMID 26314397 DOI: 10.1002/Anie.201504724 |
0.523 |
|
| 2015 |
Niu W, Yeung YY. Catalytic and highly enantioselective selenolactonization. Organic Letters. 17: 1660-3. PMID 25763679 DOI: 10.1021/Acs.Orglett.5B00377 |
0.545 |
|
| 2015 |
Yu WZ, Chen F, Cheng YA, Yeung YY. Catalyst-free and metal-free electrophilic bromoamidation of unactivated olefins using the N-bromosuccinimide/sulfonamide protocol. The Journal of Organic Chemistry. 80: 2815-21. PMID 25646563 DOI: 10.1021/Jo502416R |
0.447 |
|
| 2015 |
Zhao Y, Wong YC, Yeung YY. An unexpected 2,3-dihydrofuran derivative ring opening initiated by electrophilic bromination: scope and mechanistic study. The Journal of Organic Chemistry. 80: 453-9. PMID 25469549 DOI: 10.1021/Jo502453F |
0.517 |
|
| 2015 |
Chen T, Foo TJY, Yeung YY. Indole-Catalyzed Bromolactonization in Lipophilic Solvent: A Solid-Liquid Phase Transfer Approach Acs Catalysis. 5: 4751-4755. DOI: 10.1021/Acscatal.5B01182 |
0.453 |
|
| 2015 |
Cheng YA, Yu WZ, Yeung YY. Carbamate-Catalyzed Enantioselective Bromolactamization Angewandte Chemie - International Edition. 54: 12102-12106. DOI: 10.1002/anie.201504724 |
0.482 |
|
| 2014 |
Zhou J, Yeung YY. Diastereoselective synthesis of functionalized pyrrolidines through N-bromosuccinimide-induced aziridine ring expansion cascade of cinnamylaziridine. Organic & Biomolecular Chemistry. 12: 7482-5. PMID 25156246 DOI: 10.1039/C4Ob01384K |
0.372 |
|
| 2014 |
Zhou J, Yeung YY. Synthesis of reboxetine intermediate and carnitine acetyltransferase inhibitor via NBS-induced electrophilic multicomponent reaction. The Journal of Organic Chemistry. 79: 4644-9. PMID 24742295 DOI: 10.1021/Jo500609A |
0.469 |
|
| 2014 |
Tay DW, Leung GY, Yeung YY. Desymmetrization of diolefinic diols by enantioselective amino-thiocarbamate-catalyzed bromoetherification: synthesis of chiral spirocycles. Angewandte Chemie (International Ed. in English). 53: 5161-4. PMID 24706539 DOI: 10.1002/Anie.201310136 |
0.552 |
|
| 2014 |
Ke Z, Tan CK, Chen F, Yeung YY. Catalytic asymmetric bromoetherification and desymmetrization of olefinic 1,3-diols with C2-symmetric sulfides. Journal of the American Chemical Society. 136: 5627-30. PMID 24697791 DOI: 10.1021/Ja5029155 |
0.68 |
|
| 2014 |
Zhou J, Yeung YY. N-bromosuccinimide-induced aminocyclization-aziridine ring-expansion cascade: an asymmetric and highly stereoselective approach toward the synthesis of azepane. Organic Letters. 16: 2134-7. PMID 24689521 DOI: 10.1021/Ol5005609 |
0.419 |
|
| 2014 |
Cheng YA, Yu WZ, Yeung YY. Recent advances in asymmetric intra- and intermolecular halofunctionalizations of alkenes. Organic & Biomolecular Chemistry. 12: 2333-43. PMID 24595745 DOI: 10.1039/C3Ob42335B |
0.445 |
|
| 2014 |
Tan CK, Yu WZ, Yeung YY. Stereoselective bromofunctionalization of alkenes. Chirality. 26: 328-43. PMID 24339201 DOI: 10.1002/Chir.22272 |
0.428 |
|
| 2014 |
Zhao Y, Ng AWT, Yeung YY. Mild propargylic oxidation using a diacetoxyiodobenzene/tert-butyl hydroperoxide protocol Tetrahedron Letters. 55: 4370-4372. DOI: 10.1016/J.Tetlet.2014.06.032 |
0.37 |
|
| 2014 |
Tan CK, Er JC, Yeung YY. Synthesis of chiral butenolides using amino-thiocarbamate-catalyzed asymmetric bromolactonization Tetrahedron Letters. 55: 1243-1246. DOI: 10.1016/J.Tetlet.2014.01.009 |
0.537 |
|
| 2014 |
Zhou J, Yeung Y. ChemInform Abstract: Synthesis of Reboxetine Intermediate (IV) and Carnitine Acetyltransferase Inhibitor (VIII) via NBS-Induced Electrophilic Multicomponent Reaction. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201442048 |
0.363 |
|
| 2014 |
Tan CK, Er JC, Yeung Y. ChemInform Abstract: Synthesis of Chiral Butenolides Using Amino-thiocarbamate-catalyzed Asymmetric Bromolactonization. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201428088 |
0.39 |
|
| 2013 |
Tan CK, Yeung YY. Recent advances in stereoselective bromofunctionalization of alkenes using N-bromoamide reagents. Chemical Communications (Cambridge, England). 49: 7985-96. PMID 23903206 DOI: 10.1039/C3Cc43950J |
0.467 |
|
| 2013 |
Zhao Y, Jiang X, Yeung YY. Catalytic, enantioselective, and highly chemoselective bromocyclization of olefinic dicarbonyl compounds. Angewandte Chemie (International Ed. in English). 52: 8597-601. PMID 23852877 DOI: 10.1002/Anie.201304107 |
0.531 |
|
| 2013 |
Ke Z, Yeung YY. NBS-initiated electrophilic phenoxyetherification of olefins. Organic Letters. 15: 1906-9. PMID 23544361 DOI: 10.1021/Ol4005646 |
0.631 |
|
| 2013 |
Tay DW, Tsoi IT, Er JC, Leung GY, Yeung YY. Lewis basic selenium catalyzed chloroamidation of olefins using nitriles as the nucleophiles. Organic Letters. 15: 1310-3. PMID 23461531 DOI: 10.1021/Ol400249X |
0.577 |
|
| 2013 |
Chen F, Tan CK, Yeung YY. C2-symmetric cyclic selenium-catalyzed enantioselective bromoaminocyclization. Journal of the American Chemical Society. 135: 1232-5. PMID 23312005 DOI: 10.1021/Ja311202E |
0.544 |
|
| 2013 |
Zhou L, Tay DW, Chen J, Leung GY, Yeung YY. Enantioselective synthesis of 2-substituted and 3-substituted piperidines through a bromoaminocyclization process. Chemical Communications (Cambridge, England). 49: 4412-4. PMID 23072774 DOI: 10.1039/C2Cc36578B |
0.542 |
|
| 2013 |
Jiang X, Lim Z, Yeung Y. Studies on the ring-opening of bicyclic cyclopropanes activated by a carbonyl group Tetrahedron Letters. 54: 1798-1801. DOI: 10.1016/J.Tetlet.2013.01.053 |
0.399 |
|
| 2012 |
Zhou J, Zhou L, Yeung YY. Multicomponent approach in the synthesis of 2,2,6-trisubstituted morpholine derivatives. Organic Letters. 14: 5250-3. PMID 23020247 DOI: 10.1021/Ol3024105 |
0.435 |
|
| 2012 |
Cheng YA, Chen T, Tan CK, Heng JJ, Yeung YY. Efficient medium ring size bromolactonization using a sulfur-based zwitterionic organocatalyst. Journal of the American Chemical Society. 134: 16492-5. PMID 22998611 DOI: 10.1021/Ja307210N |
0.513 |
|
| 2012 |
Jiang X, Tan CK, Zhou L, Yeung YY. Enantioselective bromolactonization using an S-alkyl thiocarbamate catalyst. Angewandte Chemie (International Ed. in English). 51: 7771-5. PMID 22730413 DOI: 10.1002/Ange.201202079 |
0.504 |
|
| 2012 |
Tan CK, Le C, Yeung YY. Enantioselective bromolactonization of cis-1,2-disubstituted olefinic acids using an amino-thiocarbamate catalyst. Chemical Communications (Cambridge, England). 48: 5793-5. PMID 22499150 DOI: 10.1039/C2Cc31148H |
0.496 |
|
| 2012 |
Chen J, Zhou L, Yeung YY. A highly enantioselective approach towards 2-substituted 3-bromopyrrolidines. Organic & Biomolecular Chemistry. 10: 3808-11. PMID 22437158 DOI: 10.1039/C2Ob25327E |
0.475 |
|
| 2012 |
Chen J, Zhou L, Tan CK, Yeung YY. An enantioselective approach toward 3,4-dihydroisocoumarin through the bromocyclization of styrene-type carboxylic acids. The Journal of Organic Chemistry. 77: 999-1009. PMID 22175914 DOI: 10.1021/Jo202221C |
0.446 |
|
| 2012 |
Zhao Y, Chew X, Leung GY, Yeung Y. Oxidative transformation of azides to aryl nitriles using DIB/TBHP: scope and mechanistic insights Tetrahedron Letters. 53: 4766-4769. DOI: 10.1016/J.Tetlet.2012.06.131 |
0.387 |
|
| 2011 |
Chen J, Chng S, Zhou L, Yeung YY. Scope and mechanistic studies of electrophilic alkoxyetherification. Organic Letters. 13: 6456-9. PMID 22087786 DOI: 10.1021/Ol202751S |
0.451 |
|
| 2011 |
Zhou L, Chen J, Zhou J, Yeung YY. N-Bromosuccinimide promoted one-pot synthesis of guanidine: scope and mechanism. Organic Letters. 13: 5804-7. PMID 21988188 DOI: 10.1021/Ol202402Y |
0.482 |
|
| 2011 |
Zhao Y, Yim WL, Tan CK, Yeung YY. An unexpected oxidation of unactivated methylene C-H using DIB/TBHP protocol. Organic Letters. 13: 4308-11. PMID 21786789 DOI: 10.1021/Ol2016466 |
0.337 |
|
| 2011 |
Zhou L, Chen J, Tan CK, Yeung YY. Enantioselective bromoaminocyclization using amino-thiocarbamate catalysts. Journal of the American Chemical Society. 133: 9164-7. PMID 21539367 DOI: 10.1021/Ja201627H |
0.54 |
|
| 2011 |
Tan CK, Zhou L, Yeung YY. Aminothiocarbamate-catalyzed asymmetric bromolactonization of 1,2-disubstituted olefinic acids. Organic Letters. 13: 2738-41. PMID 21520898 DOI: 10.1021/Ol200840E |
0.537 |
|
| 2011 |
Zhou L, Zhou J, Tan CK, Chen J, Yeung YY. N-bromosuccinimide initiated one-pot synthesis of imidazoline. Organic Letters. 13: 2448-51. PMID 21486027 DOI: 10.1021/Ol2006902 |
0.458 |
|
| 2011 |
Chen J, Chng S, Zhou L, Yeung YY. Scope and mechanistic studies of electrophilic alkoxyetherification Organic Letters. 13: 6456-6459. DOI: 10.1021/ol202751s |
0.351 |
|
| 2011 |
Tan CK, Chen F, Yeung Y. Studies toward Lewis basic thiocarbamate and thiourea mediated bromolactonization: the effect of a trace amount of water on the reactivity and enantioselectivity Tetrahedron Letters. 52: 4892-4895. DOI: 10.1016/J.Tetlet.2011.07.049 |
0.455 |
|
| 2010 |
Zhou L, Tan CK, Jiang X, Chen F, Yeung YY. Asymmetric bromolactonization using amino-thiocarbamate catalyst. Journal of the American Chemical Society. 132: 15474-6. PMID 20945837 DOI: 10.1021/Ja1048972 |
0.592 |
|
| 2010 |
Zhou L, Tan CK, Zhou J, Yeung YY. Facile, efficient, and catalyst-free electrophilic aminoalkoxylation of olefins: scope and application. Journal of the American Chemical Society. 132: 10245-7. PMID 20662501 DOI: 10.1021/Ja104168Q |
0.603 |
|
| 2010 |
Zhao Y, Yeung YY. An unprecedented method for the generation of tert-butylperoxy radical using DIB/TBHP protocol: solvent effect and application on allylic oxidation. Organic Letters. 12: 2128-31. PMID 20387842 DOI: 10.1021/Ol100603Q |
0.352 |
|
| 2010 |
Chen F, Jiang X, Er JC, Yeung Y. Molecular sieves as an efficient and recyclable catalyst for bromolactonization and bromoacetoxylation reactions Tetrahedron Letters. 51: 3433-3435. DOI: 10.1016/J.Tetlet.2010.04.113 |
0.5 |
|
| 2010 |
Chen F, Jiang X, Er JC, Yeung Y. ChemInform Abstract: Molecular Sieves as an Efficient and Recyclable Catalyst for Bromolactonization and Bromoacetoxylation Reactions. Cheminform. 41. DOI: 10.1002/CHIN.201042036 |
0.449 |
|
| 2010 |
Chow H, Wan C, Low K, Yeung Y. ChemInform Abstract: A Highly Selective Synthesis of Diarylethynes and Their Oligomers by a Palladium-Catalyzed Sonogashira Coupling Reaction under Phase Transfer Conditions. Cheminform. 32: no-no. DOI: 10.1002/chin.200128096 |
0.388 |
|
| 2009 |
Chein RJ, Yeung YY, Corey EJ. Highly enantioselective oxazaborolidine-catalyzed reduction of 1,3-dicarbonyl compounds: role of the additive diethylaniline. Organic Letters. 11: 1611-4. PMID 19278241 DOI: 10.1021/Ol900258F |
0.625 |
|
| 2008 |
Yeung YY, Corey EJ. A simple, efficient, and enantiocontrolled synthesis of a near-structural mimic of platensimycin. Organic Letters. 10: 3877-8. PMID 18665602 DOI: 10.1021/Ol801400A |
0.392 |
|
| 2007 |
Yeung YY, Chein RJ, Corey EJ. Conversion of Torgov's synthesis of estrone into a highly enantioselective and efficient process. Journal of the American Chemical Society. 129: 10346-7. PMID 17672468 DOI: 10.1021/Ja0742434 |
0.419 |
|
| 2006 |
Shing TK, Yeung YY. Synthetic studies towards pentacyclic quassinoids: total synthesis of unnatural (-)-14-epi-samaderine E and natural (-)-samaderine Y from (S)-(+)-carvone. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 8367-77. PMID 16927353 DOI: 10.1002/CHIN.200709205 |
0.42 |
|
| 2006 |
Yeung YY, Gao X, Corey EJ. A general process for the haloamidation of olefins. Scope and mechanism. Journal of the American Chemical Society. 128: 9644-5. PMID 16866514 DOI: 10.1021/Ja063675W |
0.529 |
|
| 2006 |
Shing TK, Yeung YY, Su PL. Mild manganese(III) acetate catalyzed allylic oxidation: application to simple and complex alkenes. Organic Letters. 8: 3149-51. PMID 16805574 DOI: 10.1021/ol0612298 |
0.302 |
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| 2006 |
Yeung YY, Hong S, Corey EJ. A short enantioselective pathway for the synthesis of the anti-influenza neuramidase inhibitor oseltamivir from 1,3-butadiene and acrylic acid. Journal of the American Chemical Society. 128: 6310-1. PMID 16683783 DOI: 10.1021/Ja0616433 |
0.633 |
|
| 2001 |
Chow HF, Wan CW, Low KH, Yeung YY. A highly selective synthesis of diarylethynes and their oligomers by a palladium-catalyzed Sonogashira coupling reaction under phase transfer conditions. The Journal of Organic Chemistry. 66: 1910-3. PMID 11262146 DOI: 10.1021/Jo001538Q |
0.656 |
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