| Year |
Citation |
Score |
| 2024 |
Tang M, Lu H, Zu L. Collective total synthesis of stereoisomeric yohimbine alkaloids. Nature Communications. 15: 941. PMID 38296955 DOI: 10.1038/s41467-024-45140-2 |
0.371 |
|
| 2022 |
Chen L, Xie K, Zhang J, Zu L. Total Synthesis of Spiro[cyclohexane-2-indoline] Alkaloids: A Regio- and Diastereoselective Spirocyclization Approach. Angewandte Chemie (International Ed. in English). PMID 36224105 DOI: 10.1002/anie.202212042 |
0.397 |
|
| 2022 |
Wei B, Cheng P, Zu L. Total Synthesis of (+)-Gilbertine: A Cyclopentanone-Based Approach. Organic Letters. 24: 7320-7322. PMID 36184813 DOI: 10.1021/acs.orglett.2c02778 |
0.371 |
|
| 2021 |
Zhang Z, Zu L. Asymmetric Total Synthesis of Asperversin A. Organic Letters. PMID 33656897 DOI: 10.1021/acs.orglett.1c00366 |
0.482 |
|
| 2019 |
Wang Z, Zu L. Organocatalytic enantioselective direct alkylation of phloroglucinol derivatives: asymmetric total synthesis of (+)-aflatoxin B. Chemical Communications (Cambridge, England). PMID 30984932 DOI: 10.1039/C9Cc01833F |
0.519 |
|
| 2018 |
Yao X, Shan X, Zu L. Divergent Coupling of 2-Carbonyl-anilines and Diazo-cyclopentanones: Asymmetric Total Synthesis of (+)-Leucomidine A. Organic Letters. PMID 30270632 DOI: 10.1021/Acs.Orglett.8B02823 |
0.477 |
|
| 2018 |
Qiwen L, Zu L. Organocatalytic Enantioselective Cross-Vinylogous Rauhut-Currier Reaction of Methyl Coumalate with Enals. Angewandte Chemie (International Ed. in English). PMID 29873432 DOI: 10.1002/Anie.201805019 |
0.398 |
|
| 2018 |
Xie X, Zu L. Skeletal Rearrangements as Strategies for the Total Syntheses of Indole Alkaloids Synlett. 29: 1008-1013. DOI: 10.1055/S-0036-1591560 |
0.466 |
|
| 2017 |
Xie X, Wei B, Li G, Zu L. Unified Total Syntheses of Structurally Diverse Akuammiline Alkaloids. Organic Letters. PMID 28952737 DOI: 10.1021/Acs.Orglett.7B02698 |
0.359 |
|
| 2017 |
Yu Y, Li J, Jiang L, Zhang JR, Zu L. Catalytic Enantioselective Aza-pinacol Rearrangement. Angewandte Chemie (International Ed. in English). PMID 28618154 DOI: 10.1002/Anie.201705539 |
0.511 |
|
| 2017 |
Wang C, Wang Z, Xie X, Yao X, Li G, Zu L. Total Synthesis of (±)-Grandilodine B. Organic Letters. PMID 28294627 DOI: 10.1021/Acs.Orglett.7B00591 |
0.479 |
|
| 2017 |
Li H, Cheng P, Jiang L, Yang JL, Zu L. Bio-Inspired Fragmentations: Rapid Assembly of Indolones, 2-Quinolinones, and (-)-Goniomitine. Angewandte Chemie (International Ed. in English). PMID 28128515 DOI: 10.1002/Anie.201611830 |
0.531 |
|
| 2016 |
Jiang L, Yu Y, Li G, Zu L. Divergent Synthesis of Hydro-g-carbolines and Multi-substituted Indoles via Grob Fragmentation-Mannich Cyclization. Chemistry, An Asian Journal. PMID 27558845 DOI: 10.1002/Asia.201600980 |
0.467 |
|
| 2016 |
Li G, Xie X, Zu L. Total Synthesis of Calophyline A. Angewandte Chemie (International Ed. in English). PMID 27294980 DOI: 10.1002/Anie.201604770 |
0.529 |
|
| 2016 |
Yu Y, Li G, Zu L. The Development of Aza-Pinacol and Aza-Semipinacol Rearrangements for the Synthesis of Nitrogen-Containing Molecules Synlett. DOI: 10.1055/S-0035-1561385 |
0.512 |
|
| 2016 |
Li G, Xie X, Zu L. Back Cover: Total Synthesis of Calophyline A (Angew. Chem. Int. Ed. 35/2016) Angewandte Chemie. 55: 10524-10524. DOI: 10.1002/Anie.201606061 |
0.406 |
|
| 2016 |
Li G, Xie X, Zu L. Rücktitelbild: Total Synthesis of Calophyline A (Angew. Chem. 35/2016) Angewandte Chemie. 128: 10680-10680. DOI: 10.1002/Ange.201606061 |
0.461 |
|
| 2015 |
Yu Y, Li G, Jiang L, Zu L. An Indoxyl-Based Strategy for the Synthesis of Indolines and Indolenines. Angewandte Chemie (International Ed. in English). PMID 26315307 DOI: 10.1002/Anie.201505173 |
0.534 |
|
| 2015 |
Yao X, Xie X, Wang C, Zu L. Rapid Assembly of Functionalized Hydrodibenzofurans via Semipinacol Rearrangements. Organic Letters. 17: 4356-9. PMID 26295372 DOI: 10.1021/Acs.Orglett.5B02202 |
0.39 |
|
| 2015 |
Li H, Wang Z, Zu L. [3 + 2] Annulations between indoles and α,β-unsaturated ketones: Access to pyrrolo[1,2-a]indoles and model reactions toward the originally assigned structure of yuremamine Rsc Advances. 5: 60962-60965. DOI: 10.1039/C5Ra11904A |
0.415 |
|
| 2015 |
Jiang L, Xie X, Zu L. tert-Butyl hypochlorite mediated diastereoselective oxidative coupling: Access to 1-functionalized tetrahydrocarbazoles Rsc Advances. 5: 9204-9207. DOI: 10.1039/C4Ra14092C |
0.321 |
|
| 2014 |
Yu Y, Wang C, He X, Yao X, Zu L. Efficient assembly of polysubstituted pyrroles via a (3 + 2) cycloaddition/skeletal rearrangement/redox isomerization cascade reaction. Organic Letters. 16: 3580-3. PMID 24960109 DOI: 10.1021/Ol501580B |
0.55 |
|
| 2014 |
Zu L, Zhao Y, Gu G. Recent Development in the Synthesis of Natural Saponins and Their Derivatives Journal of Carbohydrate Chemistry. 33: 269-297. DOI: 10.1080/07328303.2014.957387 |
0.34 |
|
| 2013 |
Hong YJ, Irmisch S, Wang SC, Garms S, Gershenzon J, Zu L, Köllner TG, Tantillo DJ. Theoretical and experimental analysis of the reaction mechanism of MrTPS2, a triquinane-forming sesquiterpene synthase from chamomile. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 13590-600. PMID 23963956 DOI: 10.1002/Chem.201301018 |
0.71 |
|
| 2012 |
Zu L, Xu M, Lodewyk MW, Cane DE, Peters RJ, Tantillo DJ. Effect of isotopically sensitive branching on product distribution for pentalenene synthase: support for a mechanism predicted by quantum chemistry. Journal of the American Chemical Society. 134: 11369-71. PMID 22738258 DOI: 10.1021/Ja3043245 |
0.704 |
|
| 2011 |
Zu L, Boal BW, Garg NK. Total synthesis of (±)-aspidophylline A. Journal of the American Chemical Society. 133: 8877-9. PMID 21553860 DOI: 10.1021/Ja203227Q |
0.752 |
|
| 2011 |
Zu L, Boal BW, Garg NK. Synthesis of (±)-Aspidophylline A Synfacts. 2011: 925-925. DOI: 10.1055/S-0030-1260929 |
0.713 |
|
| 2010 |
Schammel AW, Boal BW, Zu L, Mesganaw T, Garg NK. Exploration of the interrupted Fischer indolization reaction. Tetrahedron. 66: 4687-4695. PMID 20798890 DOI: 10.1016/J.Tet.2010.02.050 |
0.602 |
|
| 2009 |
Zu L, Zhang S, Xie H, Wang W. Catalytic asymmetric oxa-Michael-Michael cascade for facile construction of chiral chromans via an aminal intermediate. Organic Letters. 11: 1627-30. PMID 19320506 DOI: 10.1021/Ol9003433 |
0.464 |
|
| 2009 |
Li H, Zu L, Xie H, Wang W. Organocatalytic EnantioselectiveConjugate Addition of 2-Fluoromalonate to Nitroolefins: Direct Synthesisof Chiral Fluorinated γ-Nitro Carboxylic Acid Derivatives Synthesis. 2009: 1525-1530. DOI: 10.1055/S-0028-1088124 |
0.35 |
|
| 2008 |
Li H, Zu L, Xie H, Wang J, Wang W. Highly enantio- and diastereoselective organocatalytic cascade aza-Michael-Michael reactions: a direct method for the synthesis of trisubstituted chiral pyrrolidines. Chemical Communications (Cambridge, England). 5636-8. PMID 18997977 DOI: 10.1039/B812464G |
0.45 |
|
| 2008 |
Zu L, Xie H, Li H, Wang J, Yu X, Wang W. Chiral amine-catalyzed enantioselective cascade aza-ene-type cyclization reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 6333-5. PMID 18546446 DOI: 10.1002/Chem.200800829 |
0.478 |
|
| 2008 |
Xie H, Zu L, Oueis HR, Li H, Wang J, Wang W. Proline-catalyzed direct inverse electron demand diels-alder reactions of ketones with 1,2,4,5-tetrazines. Organic Letters. 10: 1923-6. PMID 18410125 DOI: 10.1021/Ol800417Q |
0.443 |
|
| 2008 |
Zu L, Xie H, Li H, Wang J, Wang W. Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water. Organic Letters. 10: 1211-4. PMID 18271596 DOI: 10.1021/Ol800074Z |
0.438 |
|
| 2007 |
Wang J, Li H, Xie H, Zu L, Shen X, Wang W. Organocatalytic enantioselective cascade Michael-aldol condensation reactions: efficient assembly of densely functionalized chiral cyclopentenes. Angewandte Chemie (International Ed. in English). 46: 9050-3. PMID 17952893 DOI: 10.1002/Anie.200703163 |
0.47 |
|
| 2007 |
Xie H, Zu L, Li H, Wang J, Wang W. Organocatalytic enantioselective cascade Michael-alkylation reactions: synthesis of chiral cyclopropanes and investigation of unexpected organocatalyzed stereoselective ring opening of cyclopropanes. Journal of the American Chemical Society. 129: 10886-94. PMID 17691786 DOI: 10.1021/Ja073262A |
0.542 |
|
| 2007 |
Zu L, Li H, Xie H, Wang J, Jiang W, Tang Y, Wang W. Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions. Angewandte Chemie (International Ed. in English). 46: 3732-4. PMID 17431863 DOI: 10.1002/Anie.200700485 |
0.515 |
|
| 2007 |
Li H, Zu L, Xie H, Wang J, Jiang W, Wang W. Enantioselective organocatalytic double Michael addition reactions. Organic Letters. 9: 1833-5. PMID 17373806 DOI: 10.1021/Ol070581Y |
0.463 |
|
| 2007 |
Li H, Wang J, Xie H, Zu L, Jiang W, Duesler EN, Wang W. Chiral Diphenylprolinol TES ether promoted conjugate addition-aldol-dehydration reactions between alpha,beta-unsaturated aldehydes and 2-N-protected amino benzaldehydes. Organic Letters. 9: 965-8. PMID 17298072 DOI: 10.1021/Ol062877U |
0.42 |
|
| 2007 |
Zu L, Wang J, Li H, Xie H, Jiang W, Wang W. Cascade Michael--aldol reactions promoted by hydrogen bonding mediated catalysis. Journal of the American Chemical Society. 129: 1036-7. PMID 17263377 DOI: 10.1021/Ja067781+ |
0.432 |
|
| 2007 |
Li H, Wang J, E-Nunu T, Zu L, Jiang W, Wei S, Wang W. One-pot approach to chiral chromenes via enantioselective organocatalytic domino oxa-Michael-aldol reaction. Chemical Communications (Cambridge, England). 507-9. PMID 17252110 DOI: 10.1039/B611502K |
0.483 |
|
| 2007 |
Zu L, Xie H, Li H, Wang J, Jiang W, Wang W. Organocatalytic Domino Michael-Aldol Reaction to Chiral Benzothiopyrans Synfacts. 2007: 1132-1132. DOI: 10.1055/S-2007-991297 |
0.463 |
|
| 2007 |
Wang J, Zu L, Li H, Xie H, Wang W. Cinchona Alkaloid Based Thiourea Promoted Enantioselective Conjugate Addition of N-Heterocycles to Enones Synthesis. 2007: 2576-2580. DOI: 10.1055/S-2007-983786 |
0.477 |
|
| 2007 |
Zu L, Li H, Xie H, Wang J, Jiang W, Tang Y, Wang W. Highly Enantio- and Diastereoselective Cascade Double Michael Addition Synfacts. 2007: 758-758. DOI: 10.1055/S-2007-968633 |
0.461 |
|
| 2007 |
Wang J, Li H, Zu L, Jiang W, Wang W. Conjugate Addition of Nitroalkanes to Nitroolefins Synfacts. 2007: 215-215. DOI: 10.1055/S-2006-955792 |
0.348 |
|
| 2007 |
Zu L, Xie H, Li H, Wang J, Wang W. Highly Enantioselective Organocatalytic Conjugate Addition of Nitromethane to α,β‐Unsaturated Aldehydes: Three‐Step Synthesis of Optically Active Baclofen Advanced Synthesis & Catalysis. 349: 2660-2664. DOI: 10.1002/Adsc.200700353 |
0.446 |
|
| 2007 |
Zu L, Xie H, Li H, Wang J, Jiang W, Wang W. Chiral Amine Thiourea‐Promoted Enantioselective Domino Michael‐Aldol Reactions between 2‐Mercaptobenzaldehydes and Maleimides Advanced Synthesis & Catalysis. 349: 1882-1886. DOI: 10.1002/Adsc.200700158 |
0.434 |
|
| 2007 |
Wang J, Heikkinen LD, Li H, Zu L, Jiang W, Xie H, Wang W. Quinine‐Catalyzed Enantioselective Michael Addition of Diphenyl Phosphite to Nitroolefins: Synthesis of Chiral Precursors of α‐Substituted β‐Aminophosphonates Advanced Synthesis & Catalysis. 349: 1052-1056. DOI: 10.1002/Adsc.200600429 |
0.496 |
|
| 2006 |
Wang J, Li H, Zu L, Jiang W, Xie H, Duan W, Wang W. Organocatalytic enantioselective conjugate additions to enones. Journal of the American Chemical Society. 128: 12652-3. PMID 17002351 DOI: 10.1021/ja065187u |
0.418 |
|
| 2006 |
Wang W, Li H, Wang J, Zu L. Enantioselective organocatalytic tandem Michael-Aldol reactions: one-pot synthesis of chiral thiochromenes. Journal of the American Chemical Society. 128: 10354-5. PMID 16895386 DOI: 10.1021/Ja063328M |
0.487 |
|
| 2006 |
Zu L, Wang J, Li H, Wang W. A recyclable fluorous (S)-pyrrolidine sulfonamide promoted direct, highly enantioselective Michael addition of ketones and aldehydes to nitroolefins in water. Organic Letters. 8: 3077-9. PMID 16805556 DOI: 10.1021/Ol061053+ |
0.419 |
|
| 2006 |
Wang J, Li H, Lou B, Zu L, Guo H, Wang W. Enantio- and diastereoselective Michael addition reactions of unmodified aldehydes and ketones with nitroolefins catalyzed by a pyrrolidine sulfonamide. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 4321-32. PMID 16575937 DOI: 10.1002/Chem.200600115 |
0.439 |
|
| 2006 |
Wang J, Li H, Zu L, Wang W. Enantioselective organocatalytic Michael addition reactions between N-heterocycles and nitroolefins. Organic Letters. 8: 1391-4. PMID 16562899 DOI: 10.1021/Ol0601794 |
0.415 |
|
| 2006 |
Li H, Wang J, Zu L, Wang W. Organocatalytic One-Pot Synthesis of Chiral Thiochromenes Synfacts. 2006: 1065-1065. DOI: 10.1055/S-2006-949371 |
0.465 |
|
| 2006 |
Wang J, Li H, Zu L, Wang W. Enantioselective Michael Addition ofN-Heterocycles to Nitroolefins Synfacts. 2006: 609-609. DOI: 10.1055/S-2006-941779 |
0.479 |
|
| 2006 |
Zu L, Li H, Wang J, Yu X, Wang W. Highly enantioselective aldehyde–nitroolefin Michael addition reactions catalyzed by recyclable fluorous (S) diphenylpyrrolinol silyl ether Tetrahedron Letters. 47: 5131-5134. DOI: 10.1016/J.Tetlet.2006.05.067 |
0.448 |
|
| 2006 |
Li H, Zu L, Wang J, Wang W. Organocatalytic enantioselective Michael addition of thioacetic acid to enones Tetrahedron Letters. 47: 3145-3148. DOI: 10.1016/J.Tetlet.2006.02.140 |
0.484 |
|
| 2006 |
Li H, Wang J, Zu L, Wang W. Organocatalytic asymmetric conjugate addition of thioacetic acid to β-nitrostyrenes Tetrahedron Letters. 47: 2585-2589. DOI: 10.1016/J.Tetlet.2006.02.036 |
0.392 |
|
| 2006 |
Wang J, Li H, Zu L, Jiang W, Wang W. Organocatalytic, Enantioselective Conjugate Addition of Nitroalkanes to Nitroolefins Advanced Synthesis & Catalysis. 348: 2047-2050. DOI: 10.1002/Adsc.200600247 |
0.455 |
|
| 2006 |
Wang J, Li H, Zu L, Wang W. Highly Enantioselective Organocatalytic Michael Addition Reactions of Ketones with Chalcones Advanced Synthesis & Catalysis. 348: 425-428. DOI: 10.1002/Adsc.200505420 |
0.478 |
|
| 2005 |
Wang J, Li H, Duan W, Zu L, Wang W. Organocatalytic asymmetric Michael addition of 2,4-pentandione to nitroolefins. Organic Letters. 7: 4713-6. PMID 16209517 DOI: 10.1021/Ol0519137 |
0.469 |
|
| 2005 |
Wang J, Li H, Yu X, Zu L, Wang W. Chiral binaphthyl-derived amine-thiourea organocatalyst-promoted asymmetric Morita-Baylis-Hillman reaction. Organic Letters. 7: 4293-6. PMID 16146410 DOI: 10.1021/Ol051822+ |
0.486 |
|
| 2003 |
Jiao XZ, Xie P, Zu LS, Liang XT. Study of stereoselective synthesis of (+/-)-neocnidilide. Journal of Asian Natural Products Research. 5: 165-9. PMID 12931848 DOI: 10.1080/1028602031000066870 |
0.358 |
|
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