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Guofu Zhong, Ph.D. - Publications

Affiliations: 
Division of Chemistry and Biological Chemistry Nanyang Technological University, Singapore, Singapore 
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Year Citation  Score
2019 Pan S, Wu B, Hu J, Xu R, Jiang M, Zeng X, Zhong G. Palladium-Catalyzed Allylic Substitution Reaction of Benzothiazolylacetamide with Allylic Alcohols in Water. The Journal of Organic Chemistry. PMID 31343177 DOI: 10.1021/acs.joc.9b01313  0.4
2019 Hou Y, Hu J, Xu R, Pan S, Zeng X, Zhong G. Indium-Mediated Synthesis of Benzylic Hydroperoxides. Organic Letters. PMID 31184170 DOI: 10.1021/acs.orglett.9b01070  0.4
2018 Yang L, Lv Y, Wang F, Zhong G. Correction: Chiral NHC-catalyzed 1,3-dipolar [3 + 2] cycloaddition of azomethine imines with α-chloroaldehydes for the synthesis of bicyclic pyrazolidinones. Organic & Biomolecular Chemistry. PMID 30083663 DOI: 10.1039/c8ob90095g  0.44
2018 Yang L, Lv Y, Wang F, Zhong G. Chiral NHC-catalyzed 1,3-dipolar [3 + 2] cycloaddition of azomethine imines with α-chloroaldehydes for the synthesis of bicyclic pyrazolidinones. Organic & Biomolecular Chemistry. PMID 29846371 DOI: 10.1039/c8ob00925b  0.44
2017 Dai L, Hou Y, Zhang L, Chen Z, Zeng X, Zhong G. Construction of tetrahydropyranoquinoline derivatives via an asymmetric organocatalytic aza-Michael-IED/HAD cascade reaction. Organic & Biomolecular Chemistry. PMID 29115338 DOI: 10.1039/c7ob02231j  0.4
2017 Song W, Yan P, Shen D, Chen Z, Zeng X, Zhong G. Synthesis of Cyano-Containing Phenanthridine Derivatives via Catalyst, Base and Oxidant Free Direct Cyanoalkylarylation of Isocyanides. The Journal of Organic Chemistry. PMID 28362091 DOI: 10.1021/acs.joc.7b00343  0.4
2017 Shen D, Chen Q, Yan P, Zeng X, Zhong G. Enantioselective Dearomatization of Naphthol Derivatives with Allylic Alcohols by Cooperative Iridium and Brønsted Acid Catalysis. Angewandte Chemie (International Ed. in English). PMID 28194912 DOI: 10.1002/anie.201609693  0.4
2016 Li F, Yu C, Zhang J, Zhong G. Olefination of Electron-Deficient Alkenes with Allyl Acetate: Stereo- and Regioselective Access to (2Z,4E)-Dienamides. Organic Letters. PMID 27583399 DOI: 10.1021/acs.orglett.6b02229  0.88
2016 Xie D, Shen D, Chen Q, Zhou J, Zeng X, Zhong G. N-Heterocyclic Carbene/Lewis Acid Catalyzed Enantioselective Aerobic Annulation of alpha,beta-Unsaturated Aldehydes with 1,3-Dicarbonyl Compounds. The Journal of Organic Chemistry. PMID 27337175 DOI: 10.1021/acs.joc.6b01152  0.88
2016 Zhu L, Chen Q, Shen D, Zhang W, Shen C, Zeng X, Zhong G. Enantioselective Construction of Spirocyclic Oxindole Derivatives with Multiple Stereocenters via an Organocatalytic Michael/Aldol/Hemiacetalization Cascade Reaction. Organic Letters. PMID 27145022 DOI: 10.1021/acs.orglett.6b00873  0.4
2016 Liu W, Lu Y, Zhong G, Jiang B, Pan Z. Clinical and MRI evaluation of anxiety as the first symptom of sporadic creutzfeldt-jakob disease: A case report Experimental and Therapeutic Medicine. 11: 1513-1515. DOI: 10.3892/etm.2016.3041  0.4
2016 Cheng H, Zhang R, Yang S, Wang M, Zeng X, Xie L, Xie C, Wu J, Zhong G. Assembly of Enantioenriched cis-3a,8a-Hexahydropyrrolo[2,3-b]indole Scaffolds by Silver(I)-Catalyzed Asymmetric Domino Reaction of Isocyanoacetates in the Presence of Cinchona-Derived Chiral Phosphorus Ligands Advanced Synthesis and Catalysis. DOI: 10.1002/adsc.201500538  0.4
2015 Zhang Z, Zeng X, Xie D, Chen D, Ding L, Wang A, Yang L, Zhong G. N-Heterocyclic Carbene-Catalyzed Activation of Esters of N-Hydroxyphthalimide: A Highly Enantioselective Route to Chiral Dihydropyridinones Bearing an All Carbon Quaternary Stereogenic Center. Organic Letters. PMID 26439608 DOI: 10.1021/acs.orglett.5b02527  0.88
2015 Liu S, Tan B, Dai C, Lou S, Tao A, Zhong G. Geochemical characterization and heavy metal migration in a coastal polluted aquifer incorporating tidal effects: field investigation in Chongming Island, China. Environmental Science and Pollution Research International. PMID 26300351 DOI: 10.1007/s11356-015-5010-9  0.4
2015 Wang Z, Yang X, Cai J, Shi H, Zhong G, Chi H. Vascular endothelial function of patients with stable coronary artery disease. Pakistan Journal of Medical Sciences. 31: 538-42. PMID 26150839 DOI: 10.12669/pjms.313.6892  0.44
2015 Wang F, Zheng H, Zhang G, Ding Z, Li F, Zhong G, Chen Y, Jia Y, Miao N, Wu Z, Sun X, Li L, Liang X, Cui F. Effectiveness of prevention of mother-to-child transmission practice in three provinces of Southern China. Human Vaccines & Immunotherapeutics. 0. PMID 26090956 DOI: 10.1080/21645515.2015.1023972  0.44
2015 Cheng C, Zhang L, Yang X, Zhong G. Profiling gene expression in citrus fruit calyx abscission zone (AZ-C) treated with ethylene. Molecular Genetics and Genomics : Mgg. PMID 25948248 DOI: 10.1007/s00438-015-1054-2  0.44
2015 Xie D, Yang L, Lin Y, Zhang Z, Chen D, Zeng X, Zhong G. Rapid access to spirocylic oxindoles: application of asymmetric N-heterocyclic carbene-catalyzed [3 + 3] cycloaddition of imines to oxindole-derived enals. Organic Letters. 17: 2318-21. PMID 25939021 DOI: 10.1021/acs.orglett.5b00726  0.88
2015 Zhou H, Zeng X, Ding L, Xie Y, Zhong G. Triflic Acid catalyzed formal [3 + 2] cycloaddition of donor-acceptor oxiranes and nitriles: a facile access to 3-oxazolines. Organic Letters. 17: 2385-7. PMID 25938163 DOI: 10.1021/acs.orglett.5b00911  0.88
2015 Lin Y, Yang L, Deng Y, Zhong G. Cooperative catalysis of N-heterocyclic carbene and Brønsted acid for a highly enantioselective route to unprotected spiro-indoline-pyrans. Chemical Communications (Cambridge, England). 51: 8330-3. PMID 25882587 DOI: 10.1039/c5cc02096d  0.88
2015 Wang R, Zhong G, Zhou W, Li L, Yang H, Wang F. A model for predicting cutting depth of casing using AWJ technique based on gene expression programming algorithm Zhongguo Shiyou Daxue Xuebao (Ziran Kexue Ban)/Journal of China University of Petroleum (Edition of Natural Science). 39: 60-65. DOI: 10.3969/j.issn.1673-5005.2015.01.008  0.44
2015 Zhou H, Zeng X, Xie Y, Zhong G. Synthesis of 3-Oxazolines via SnCl4-Promoted Formal [3+2] Cycloaddition of Donor-Acceptor Oxiranes and Nitriles Synlett. 26: 1693-1696. DOI: 10.1055/s-0034-1380216  0.4
2015 Liu S, Tan B, Dai C, Lou S, Tao A, Zhong G. Geochemical characterization and heavy metal migration in a coastal polluted aquifer incorporating tidal effects: field investigation in Chongming Island, China Environmental Science and Pollution Research. DOI: 10.1007/s11356-015-5010-9  0.4
2014 Hu ZM, Xie XF, Chen ZJ, Peng XY, Du TF, Cui ZQ, Ge LJ, Li T, Yuan X, Zhang X, Hu LQ, Zhong GQ, Lin SY, Wan BN, Gorini G, et al. Monte Carlo simulation of a Bonner sphere spectrometer for application to the determination of neutron field in the Experimental Advanced Superconducting Tokamak experimental hall. The Review of Scientific Instruments. 85: 11E417. PMID 25430324 DOI: 10.1063/1.4891163  0.48
2014 Du TF, Chen ZJ, Peng XY, Yuan X, Zhang X, Gorini G, Nocente M, Tardocchi M, Hu ZM, Cui ZQ, Xie XF, Ge LJ, Hu LQ, Zhong GQ, Lin SY, et al. Design of the radiation shielding for the time of flight enhanced diagnostics neutron spectrometer at Experimental Advanced Superconducting Tokamak. The Review of Scientific Instruments. 85: 11E115. PMID 25430294 DOI: 10.1063/1.4891059  0.48
2014 Peng XY, Chen ZJ, Zhang X, Hu ZM, Du TF, Cui ZQ, Xie XF, Ge LJ, Yuan X, Gorini G, Nocente M, Tardocchi M, Hu LQ, Zhong GQ, Lin SY, et al. Light output function and assembly of the time-of-flight enhanced diagnostics neutron spectrometer plastic scintillators for background reduction by double kinematic selection at EAST. The Review of Scientific Instruments. 85: 11E112. PMID 25430291 DOI: 10.1063/1.4886762  0.48
2014 Chen ZJ, Peng XY, Zhang X, Du TF, Hu ZM, Cui ZQ, Ge LJ, Xie XF, Yuan X, Gorini G, Nocente M, Tardocchi M, Hu LQ, Zhong GQ, Lin SY, et al. Data acquisition system with pulse height capability for the TOFED time-of-flight neutron spectrometer. The Review of Scientific Instruments. 85: 11D830. PMID 25430243 DOI: 10.1063/1.4885474  0.48
2014 Cui ZQ, Chen ZJ, Xie XF, Peng XY, Hu ZM, Du TF, Ge LJ, Zhang X, Yuan X, Xia ZW, Hu LQ, Zhong GQ, Lin SY, Wan BN, Fan TS, et al. Design of a magnetic shielding system for the time of flight enhanced diagnostics neutron spectrometer at Experimental Advanced Superconducting Tokamak. The Review of Scientific Instruments. 85: 11D829. PMID 25430242 DOI: 10.1063/1.4890536  0.48
2014 Meng Q, Wang S, Wang Y, Wan S, Liu K, Zhou X, Zhong G, Zhang X, Chen X. Arterial stiffness is a potential mechanism and promising indicator of orthostatic hypotension in the general population. Vasa. Zeitschrift FüR GefäSskrankheiten. 43: 423-32. PMID 25339160 DOI: 10.1024/0301-1526/a000389  0.48
2014 Yang L, Wang F, Lee R, Lv Y, Huang KW, Zhong G. Asymmetric NHC-catalyzed aza-Diels-Alder reactions: highly enantioselective route to α-amino acid derivatives and DFT calculations. Organic Letters. 16: 3872-5. PMID 24987938 DOI: 10.1021/ol501424f  0.88
2014 Tan B, Zhang X, Zhong G. Protecting-group directed stereospecific organocatalytic [3+2] cycloadditions: A facile access to chiral spirocyclic oxindoles Arkivoc. 2014: 124-142. DOI: 10.3998/ark.5550190.p008.401  0.88
2012 Lipshutz BH, Huang S, Leong WW, Zhong G, Isley NA. C-C bond formation via copper-catalyzed conjugate addition reactions to enones in water at room temperature. Journal of the American Chemical Society. 134: 19985-8. PMID 23190029 DOI: 10.1021/ja309409e  0.88
2012 Shi Z, Yu P, Loh TP, Zhong G. Catalytic asymmetric [4+2] annulation initiated by an aza-Rauhut-Currier reaction: facile entry to highly functionalized tetrahydropyridines. Angewandte Chemie (International Ed. in English). 51: 7825-9. PMID 22833412 DOI: 10.1002/anie.201203316  0.88
2012 Shi Z, Tong Q, Leong WW, Zhong G. [4+2] annulation of vinyl ketones initiated by a phosphine-catalyzed aza-Rauhut-Currier reaction: a practical access to densely functionalized tetrahydropyridines. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 9802-6. PMID 22740243 DOI: 10.1002/chem.201201318  0.88
2012 Yang L, Wang F, Chua PJ, Lv Y, Zhong LJ, Zhong G. N-heterocyclic carbene (NHC)-catalyzed highly diastereo- and enantioselective oxo-Diels-Alder reactions for synthesis of fused pyrano[2,3-b]indoles. Organic Letters. 14: 2894-7. PMID 22594458 DOI: 10.1021/ol301175z  0.88
2012 Tan B, Zeng X, Leong WW, Shi Z, Barbas CF, Zhong G. Core structure-based design of organocatalytic [3+2]-cycloaddition reactions: highly efficient and stereocontrolled syntheses of 3,3'-pyrrolidonyl spirooxindoles. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 63-7. PMID 22162076 DOI: 10.1002/chem.201103449  0.88
2011 Lu M, Lu Y, Tan PKA, Lau QY, Zhong G. Highly enantioselective synthesis of fluorinated β-amino ketones via asymmetric organocatalytic Mannich reactions: A case study of unusual reversal of regioselectivity Synlett. 477-480. DOI: 10.1055/s-0030-1259513  0.88
2010 Shi Z, Tan B, Leong WW, Zeng X, Lu M, Zhong G. Catalytic asymmetric formal [4 + 1] annulation leading to optically active cis-isoxazoline N-oxides. Organic Letters. 12: 5402-5. PMID 20958089 DOI: 10.1021/ol102181r  0.88
2010 Chua PJ, Tan B, Yang L, Zeng X, Zhu D, Zhong G. Highly stereoselective synthesis of indanes with four stereogenic centers via sequential Michael reaction and [3+2] cycloaddition. Chemical Communications (Cambridge, England). 46: 7611-3. PMID 20838691 DOI: 10.1039/c0cc01577f  0.88
2010 Lu M, Lu Y, Zhu D, Zeng X, Li X, Zhong G. Chiral Brønsted acid catalyzed enantioselective α-aminoxylation of enecarbamates. Angewandte Chemie (International Ed. in English). 49: 8588-92. PMID 20661978 DOI: 10.1002/anie.201002640  0.88
2010 Tan B, Lu Y, Zeng X, Chua PJ, Zhong G. Facile domino access to chiral bicyclo[3.2.1]octanes and discovery of a new catalytic activation mode. Organic Letters. 12: 2682-5. PMID 20469881 DOI: 10.1021/ol1007795  0.88
2010 Zeng X, Ye K, Lu M, Chua PJ, Tan B, Zhong G. Chiral Brønsted acid catalyzed enantioselective addition of alpha-isocyanoacetamides to aldehydes. Organic Letters. 12: 2414-7. PMID 20429535 DOI: 10.1021/ol1007789  0.88
2010 Xu ZJ, Zhu D, Zeng X, Wang F, Tan B, Hou Y, Lv Y, Zhong G. Diastereoselective HOTf-catalyzed three-component one-pot 1,3-dipolar cycloaddition of alpha-diazo ester, nitrosobenzene and electron-deficient alkene. Chemical Communications (Cambridge, England). 46: 2504-6. PMID 20309476 DOI: 10.1039/b924575h  0.88
2010 Tan B, Zhu D, Zhang L, Chua PJ, Zeng X, Zhong G. Water--more than just a green solvent: a stereoselective one-pot access to all-chiral tetrahydronaphthalenes in aqueous media. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 3842-8. PMID 20151437 DOI: 10.1002/chem.200902932  0.88
2009 Sun H, Kong R, Zhu D, Lu M, Ji Q, Liew CW, Lescar J, Zhong G, Liang ZX. Products of the iterative polyketide synthases in 9- and 10-membered enediyne biosynthesis. Chemical Communications (Cambridge, England). 7399-401. PMID 20024241 DOI: 10.1039/b916751j  0.88
2009 Zhu D, Lu M, Dai L, Zhong G. Highly stereoselective one-pot synthesis of bicyclic isoxazolidines with five stereogenic centers by an organocatalytic process. Angewandte Chemie (International Ed. in English). 48: 6089-92. PMID 19598191 DOI: 10.1002/anie.200901249  0.88
2009 Zeng X, Zeng X, Xu Z, Lu M, Zhong G. Highly efficient asymmetric trans-selective aziridination of diazoacetamides and N-Boc-imines catalyzed by chiral Brønsted acids. Organic Letters. 11: 3036-9. PMID 19534488 DOI: 10.1021/ol901047w  0.88
2009 Chua PJ, Tan B, Zeng X, Zhong G. L-prolinol as a highly enantioselective catalyst for Michael addition of cyclohexanone to nitroolefins. Bioorganic & Medicinal Chemistry Letters. 19: 3915-8. PMID 19359171 DOI: 10.1016/j.bmcl.2009.03.076  0.88
2009 Tan B, Zeng X, Lu Y, Chua PJ, Zhong G. Rational design of organocatalyst: highly stereoselective Michael addition of cyclic ketones to nitroolefins. Organic Letters. 11: 1927-30. PMID 19344184 DOI: 10.1021/ol900330p  0.88
2009 Tan B, Zhang X, Chua PJ, Zhong G. Recyclable organocatalysis: highly enantioselective Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins. Chemical Communications (Cambridge, England). 779-81. PMID 19322439 DOI: 10.1039/b813915f  0.88
2009 Lu M, Zhu D, Lu Y, Zeng X, Tan B, Xu Z, Zhong G. Chiral Brønsted acid-catalyzed enantioselective alpha-hydroxylation of beta-dicarbonyl compounds. Journal of the American Chemical Society. 131: 4562-3. PMID 19290662 DOI: 10.1021/ja8088907  0.88
2009 Yang L, Tan B, Wang F, Zhong G. An unexpected N-heterocyclic carbene-catalyzed annulation of enals and nitroso compounds. The Journal of Organic Chemistry. 74: 1744-6. PMID 19170534 DOI: 10.1021/jo802515g  0.88
2009 Tan B, Shi Z, Chua PJ, Li Y, Zhong G. Unusual domino michael/aldol condensation reactions employing oximes as N-selective nucleophiles: synthesis of N-hydroxypyrroles. Angewandte Chemie (International Ed. in English). 48: 758-61. PMID 19130437 DOI: 10.1002/anie.200805205  0.88
2009 Zeng X, Zhong G. Prolinol sulfinyl ester derivatives: Organocatalytic Michael addition of ketones to nitroolefins under neat conditions Synthesis. 1545-1550. DOI: 10.1055/s-0029-1216637  0.88
2009 Chua PJ, Tan B, Zhong G. Highly enantioselective l-thiaproline catalyzed α-aminoxylation of aldehydes in aqueous media Green Chemistry. 11: 543-547. DOI: 10.1039/b817950f  0.88
2009 Shi Z, Yu P, Chua PJ, Zhong G. Organocatalytic asymmetric synthesis of protected α,β-diamino acids Advanced Synthesis and Catalysis. 351: 2797-2800. DOI: 10.1002/adsc.200900580  0.88
2008 Lu M, Zhu D, Lu Y, Hou Y, Tan B, Zhong G. Organocatalytic asymmetric alpha-aminoxylation/aza-Michael reactions for the synthesis of functionalized tetrahydro-1,2-oxazines. Angewandte Chemie (International Ed. in English). 47: 10187-91. PMID 18846534 DOI: 10.1002/anie.200803731  0.88
2008 Zhu D, Lu M, Chua PJ, Tan B, Wang F, Yang X, Zhong G. A highly stereoselective organocatalytic tandem aminoxylation/aza-Michael reaction for the synthesis of tetrahydro-1,2-oxazines. Organic Letters. 10: 4585-8. PMID 18788743 DOI: 10.1021/ol801864c  0.88
2008 Tan B, Chua PJ, Zeng X, Lu M, Zhong G. A highly diastereo- and enantioselective synthesis of multisubstituted cyclopentanes with four chiral carbons by the organocatalytic domino Michael-Henry reaction. Organic Letters. 10: 3489-92. PMID 18630924 DOI: 10.1021/ol801273x  0.88
2008 Tan B, Shi Z, Chua PJ, Zhong G. Control of four stereocenters in an organocatalytic domino double Michael reaction: efficient synthesis of multisubstituted cyclopentanes. Organic Letters. 10: 3425-8. PMID 18616339 DOI: 10.1021/ol801246m  0.88
2008 Tan B, Chua PJ, Li Y, Zhong G. Organocatalytic asymmetric tandem Michael-Henry reactions: a highly stereoselective synthesis of multifunctionalized cyclohexanes with two quaternary stereocenters. Organic Letters. 10: 2437-40. PMID 18489178 DOI: 10.1021/ol8007183  0.88
2008 Zhu D, Lu M, Chua PJ, Tan B, Wang F, Yang X, Zhong G. A highly stereoselective organocatalytic tandem aminoxylation/Aza-Michael reaction for the synthesis of tetrahydro-1,2-oxazines (Organic Letters (2008) 10) Organic Letters. 10: 5629. DOI: 10.1021/ol802567n  0.88
2004 Zhu X, Tanaka F, Hu Y, Heine A, Fuller R, Zhong G, Olson AJ, Lerner RA, Barbas CF, Wilson IA. The origin of enantioselectivity in aldolase antibodies: crystal structure, site-directed mutagenesis, and computational analysis. Journal of Molecular Biology. 343: 1269-80. PMID 15491612 DOI: 10.1016/j.jmb.2004.08.102  0.88
2004 Zhong G, Yu Y. Enantioselective synthesis of allylic alcohols by the sequential aminoxylation-olefination reactions of aldehydes under ambient conditions. Organic Letters. 6: 1637-9. PMID 15128255 DOI: 10.1021/ol049524k  0.88
2004 Zhong G. Tandem aminoxylation-allylation reactions: a rapid, asymmetric conversion of aldehydes to mono-substituted 1,2-diols. Chemical Communications (Cambridge, England). 606-7. PMID 14973630 DOI: 10.1039/b314356b  0.88
2004 Zhong G, Fan J, Barbas CF. Amino alcohol catalyzed direct asymmetric aldol reactions: Enantioselective synthesis of anti-α-fluoro-β-hydroxy ketones Tetrahedron Letters. 45: 5681-5684. DOI: 10.1016/j.tetlet.2004.05.107  0.88
2004 Notz W, Watanabe SI, Chowdari NS, Zhong G, Betancort JM, Tanaka F, Barbas CF. The scope of the direct proline-catalyzed asymmetric addition of ketones to imines Advanced Synthesis and Catalysis. 346: 1131-1140. DOI: 10.1002/adsc.200404114  0.88
2003 Zhong G. A facile and rapid route to highly enantiopure 1,2-diols by novel catalytic asymmetric alpha-aminoxylation of aldehydes. Angewandte Chemie (International Ed. in English). 42: 4247-50. PMID 14502748 DOI: 10.1002/anie.200352097  0.88
2002 Córdova A, Notz W, Zhong G, Betancort JM, Barbas CF. A highly enantioselective amino acid-catalyzed route to functionalized alpha-amino acids. Journal of the American Chemical Society. 124: 1842-3. PMID 11866583 DOI: 10.1021/ja017270h  0.88
2001 Notz W, Sakthivel K, Bui T, Zhong G, Barbas CF. Amine-catalyzed direct asymmetric Mannich-type reactions Tetrahedron Letters. 42: 199-201. DOI: 10.1016/S0040-4039(00)01908-0  0.88
2000 Karlstrom A, Zhong G, Rader C, Larsen NA, Heine A, Fuller R, List B, Tanaka F, Wilson IA, Barbas CF, Lerner RA. Using antibody catalysis to study the outcome of multiple evolutionary trials of a chemical task. Proceedings of the National Academy of Sciences of the United States of America. 97: 3878-83. PMID 10760259 DOI: 10.1073/pnas.97.8.3878  0.88
1999 Zhong G, Lerner RA, Barbas III. Broadening the Aldolase Catalytic Antibody Repertoire by Combining Reactive Immunization and Transition State Theory: New Enantio- and Diastereoselectivities. Angewandte Chemie (International Ed. in English). 38: 3738-3741. PMID 10649343 DOI: 10.1002/(SICI)1521-3773(19991216)38:24<3738::AID-ANIE3738>3.0.CO;2-2  0.88
1999 List B, Shabat D, Zhong G, Turner JM, Li A, Bui T, Anderson J, Lerner RA, Barbas CF. A catalytic enantioselective route to hydroxy-substituted quaternary carbon centers: Resolution of tertiary aldols with a catalytic antibody Journal of the American Chemical Society. 121: 7283-7291. DOI: 10.1021/ja991507g  0.88
1998 Zhong G, Shabat D, List B, Anderson J, Sinha SC, Lerner RA, Barbas Iii CF. Catalytic Enantioselective Retro-Aldol Reactions: Kinetic Resolution of β-Hydroxyketones with Aldolase Antibodies. Angewandte Chemie (International Ed. in English). 37: 2481-2484. PMID 29711357 DOI: 10.1002/(SICI)1521-3773(19981002)37:18<2481::AID-ANIE2481>3.0.CO;2-T  0.88
1998 Hoffmann T, Zhong G, List B, Shabat D, Anderson J, Gramatikova S, Lerner RA, Barbas CF. Aldolase antibodies of remarkable scope Journal of the American Chemical Society. 120: 2768-2779. DOI: 10.1021/ja973676b  0.88
1998 Zhong G, Shabat D, List B, Anderson J, Sinha SC, Lerner RA, Barbas CF. Catalytic enantioselective retro-aldol reactions: Kinetic resolution of β-hydroxyketones with aldolase antibodies Angewandte Chemie - International Edition. 37: 2481-2484. DOI: 10.1002/(SICI)1521-3773(19981002)37:18<2481::AID-ANIE2481>3.0.CO;2-T  0.88
1997 Barbas CF, Heine A, Zhong G, Hoffmann T, Gramatikova S, Björnestedt R, List B, Anderson J, Stura EA, Wilson IA, Lerner RA. Immune versus natural selection: antibody aldolases with enzymic rates but broader scope. Science (New York, N.Y.). 278: 2085-92. PMID 9405338 DOI: 10.1126/science.278.5346.2085  0.88
1997 Zhong G, Hoffmann T, Lerner RA, Danishefsky S, Barbas CF. Antibody-catalyzed enantioselective Robinson annulation Journal of the American Chemical Society. 119: 8131-8132. DOI: 10.1021/ja970944x  0.88
1996 Björnestedt R, Zhong G, Lerner RA, Barbas CF. Copying nature's mechanism for the decarboxylation of β-keto acids into catalytic antibodies by reactive immunization Journal of the American Chemical Society. 118: 11720-11724. DOI: 10.1021/ja9620797  0.88
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