| Year |
Citation |
Score |
| 2023 |
Zhang T, Zhang C, Lu X, Peng C, Zhang Y, Zhu X, Zhong G, Zhang J. Synthesis of silyl indenes by ruthenium-catalyzed aldehyde- and acylsilane-enabled C-H alkylation/cyclization. Organic & Biomolecular Chemistry. PMID 38099332 DOI: 10.1039/d3ob01699d |
0.324 |
|
| 2023 |
Liao Y, Zhang C, Wang Y, Hu Y, Ding L, Zhong L, Zhong G, Zhang J. Chelation-assisted iridium-catalyzed hydroalkenylation and hydroarylation/cyclization with conjugated trienes. Organic & Biomolecular Chemistry. PMID 37042643 DOI: 10.1039/d3ob00166k |
0.344 |
|
| 2023 |
Chen X, He P, Xia S, Cui L, Zhong G, Yang L. NHC-Activations on α-, β-, γ-, and Beyond. Chemical Record (New York, N.Y.). e202200279. PMID 36916715 DOI: 10.1002/tcr.202200279 |
0.3 |
|
| 2023 |
Chen X, Xia S, Hu X, Zhong G, Yang L. Chiral NHC-Catalyzed [4+2] Cycloadditions: Highly Diastereo/Enantioselective Access to Spiro[cyclohex-4-ene-1,3'-indoles] and DFT Calculations. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 36638350 DOI: 10.1002/chem.202203818 |
0.361 |
|
| 2022 |
Dai L, Liu Y, Xu Q, Wang M, Zhu Q, Yu P, Zhong G, Zeng X. A Dynamic Kinetic Resolution Approach to Axially Chiral Diaryl Ethers by Catalytic Atroposelective Transfer Hydrogenation. Angewandte Chemie (International Ed. in English). e202216534. PMID 36536515 DOI: 10.1002/anie.202216534 |
0.395 |
|
| 2021 |
Tan B, An QJ, Xia W, Ding WY, Liu HH, Xiang SH, Wang YB, Zhong G. Nitrosobenzene-Enabled Chiral Phosphoric Acid Catalyzed Enantioselective Construction of Atropisomeric N-Arylbenzimidazoles. Angewandte Chemie (International Ed. in English). PMID 34553823 DOI: 10.1002/anie.202111251 |
0.494 |
|
| 2021 |
Lu J, Xu R, Zeng H, Zhong G, Wang M, Ni Z, Zeng X. Synthesis of C5-Allylindoles through an Iridium-Catalyzed Asymmetric Allylic Substitution/Oxidation Reaction Sequence of -Alkyl Indolines. Organic Letters. PMID 33848171 DOI: 10.1021/acs.orglett.1c00810 |
0.399 |
|
| 2020 |
Tan B, Zhang L, Shen J, Wu S, Zhong G, Wang YB. Design and Atroposelective Construction of IAN analogues via Organocatalytic Asymmetric Heteroannulation of Alkynes. Angewandte Chemie (International Ed. in English). PMID 32886439 DOI: 10.1002/Anie.202010598 |
0.612 |
|
| 2020 |
Lu X, Zhang J, Xu L, Shen W, Yu F, Ding L, Zhong G. Ruthenium-Catalyzed Brook Rearrangement Involved Domino Sequence Enabled by Acylsilane-Aldehyde Corporation. Organic Letters. PMID 32633529 DOI: 10.1021/Acs.Orglett.0C01983 |
0.451 |
|
| 2020 |
Xu R, Li K, Wang J, Lu J, Pan L, Zeng X, Zhong G. Direct enantioselective allylic substitution of 4-hydroxycoumarin derivatives with branched allylic alcohols via iridium catalysis. Chemical Communications (Cambridge, England). PMID 32578601 DOI: 10.1039/D0Cc02832K |
0.505 |
|
| 2020 |
Hu J, Pan S, Zhu S, Yu P, Xu R, Zhong G, Zeng X. Pd-Catalyzed Dearomative Asymmetric Allylic Alkylation of Naphthols with Alkoxyallenes. The Journal of Organic Chemistry. PMID 32466648 DOI: 10.1021/Acs.Joc.0C00582 |
0.397 |
|
| 2020 |
Huang Y, Xu L, Yu F, Shen W, Lu X, Ding L, Zhong L, Zhong G, Zhang J. Stereo-Selective and Atom-Economic Alkenyl C-H Allylation/ Alkenylation in Aqueous Media by Iridium Catalysis. The Journal of Organic Chemistry. PMID 32372645 DOI: 10.1021/Acs.Joc.0C00619 |
0.486 |
|
| 2020 |
Yan J, Song Z, Zhao C, Shi K, Yang L, Zhong G. Highly Chemoselective and Enantioselective Synthesis of 3,4-2-Pyrindin-2-ones by an NHC-Catalyzed [3 + 3] Cyclization. Organic Letters. PMID 32157889 DOI: 10.1021/Acs.Orglett.0C00699 |
0.523 |
|
| 2020 |
Pan S, Jiang M, Hu J, Xu R, Zeng X, Zhong G. Synthesis of 1,2-amino alcohols by decarboxylative coupling of amino acid derived α-amino radicals to carbonyl compounds via visible-light photocatalyst in water Green Chemistry. 22: 336-341. DOI: 10.1039/C9Gc03470F |
0.409 |
|
| 2019 |
Shen C, Lu X, Zhang J, Ding L, Sun Y, Zhong G. Bidentate auxiliary-directed alkenyl C-H allylation via exo-palladacycles: synthesis of branched 1,4-dienes. Chemical Communications (Cambridge, England). PMID 31657377 DOI: 10.1039/C9Cc07466J |
0.393 |
|
| 2019 |
Meng K, Sun Y, Zhang J, Zhang K, Ji X, Ding L, Zhong G. Iridium-Catalyzed Cross-Coupling Reactions of Alkenes by Hydrogen Transfer. Organic Letters. PMID 31589451 DOI: 10.1021/Acs.Orglett.9B02935 |
0.371 |
|
| 2019 |
Li T, Shen C, Sun Y, Zhang J, Xiang P, Lu X, Zhong G. Cobalt-Catalyzed Olefinic C-H Alkenylation/Alkylation Switched by Carbonyl Groups. Organic Letters. PMID 31518143 DOI: 10.1021/Acs.Orglett.9B02717 |
0.382 |
|
| 2019 |
Zhao C, Shi K, He G, Gu Q, Ru Z, Yang L, Zhong G. NHC-Catalyzed Asymmetric Formal [4 + 2] Annulation To Construct Spirocyclohexane Pyrazolone Skeletons. Organic Letters. PMID 31513417 DOI: 10.1021/Acs.Orglett.9B02927 |
0.518 |
|
| 2019 |
Xu L, Meng K, Zhang J, Sun Y, Lu X, Li T, Jiang Y, Zhong G. Iridium-catalyzed alkenyl C-H allylation using conjugated dienes. Chemical Communications (Cambridge, England). PMID 31353380 DOI: 10.1039/C9Cc04419A |
0.393 |
|
| 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 |
0.454 |
|
| 2019 |
Sun Y, Meng K, Zhang J, Jin M, Huang N, Zhong G. Additive- and Ligand-Free Cross-Coupling Reactions between Alkenes and Alkynes by Iridium Catalysis. Organic Letters. PMID 31188008 DOI: 10.1021/Acs.Orglett.9B01766 |
0.453 |
|
| 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 |
0.462 |
|
| 2019 |
Zhang L, Hu J, Xu R, Pan S, Zeng X, Zhong G. Catalytic Asymmetric Dearomative [3+2] Cyclisation of 1,4‐Quinone with 2,3‐Disubstituted Indoles Advanced Synthesis & Catalysis. 361: 5449-5457. DOI: 10.1002/Adsc.201901035 |
0.458 |
|
| 2019 |
Yan P, Pan S, Hu J, Lu L, Zeng X, Zhong G. Palladium Catalyzed Controllable Mono‐ or Di‐Allylic Substitution Reaction of Benzothiazolylacetate with Allylic Alcohols Advanced Synthesis & Catalysis. 361: 1322-1334. DOI: 10.1002/Adsc.201801351 |
0.4 |
|
| 2018 |
Lu X, Shen C, Meng K, Zhao L, Li T, Sun Y, Zhang J, Zhong G. Acylsilane directed aromatic C-H alkenylations by ruthenium catalysis. Chemical Communications (Cambridge, England). PMID 30574981 DOI: 10.1039/C8Cc08250B |
0.448 |
|
| 2018 |
Zhang L, Wu B, Chen Z, Hu J, Zeng X, Zhong G. Chiral phosphoric acid catalyzed enantioselective N-alkylation of indoles with in situ generated cyclic N-acyl ketimines. Chemical Communications (Cambridge, England). PMID 30065995 DOI: 10.1039/C8Cc05073B |
0.46 |
|
| 2018 |
Yan J, Sun R, Shi K, Li K, Yang L, Zhong G. NHC-Catalyzed Asymmetric Benzoin Reaction in Water. The Journal of Organic Chemistry. PMID 29888917 DOI: 10.1021/Acs.Joc.8B00481 |
0.467 |
|
| 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 |
0.507 |
|
| 2018 |
Zhao L, Zhang J, Zhong G, Chen Y, Wang S, Rong C, Liu T, Sun H, Wang Y. A Metal-Free Synthesis of 3-Phenoxyimidazo Heterocycles by Catalytic Oxidative Cyclization of 2-Amino-azaarenes with Lignin Models Synthesis. 50: 3169-3176. DOI: 10.1055/S-0037-1610139 |
0.394 |
|
| 2017 |
Yan J, Shi K, Zhao C, Ding L, Jiang S, Yang L, Zhong G. NHC-catalyzed [4+2] cycloaddition reactions for the synthesis of 3'-spirocyclic oxindoles via a C-F bond cleavage protocol. Chemical Communications (Cambridge, England). PMID 29250627 DOI: 10.1039/C7Cc08048D |
0.455 |
|
| 2017 |
Li T, Zhang J, Yu C, Lu X, Xu L, Zhong G. Ruthenium-catalyzed olefinic C-H alkenylation of enol-carbamates: highly stereo-selective synthesis of (Z,Z) and (Z,E)-butadienes. Chemical Communications (Cambridge, England). PMID 29154384 DOI: 10.1039/C7Cc07777G |
0.442 |
|
| 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 |
0.482 |
|
| 2017 |
Jiang S, Li K, Yan J, Shi K, Zhao C, Yang L, Zhong G. Synthetic Access to Oxazolidin-4-ones via Elimination/[3+2] Cycloaddition Reaction. The Journal of Organic Chemistry. PMID 28829132 DOI: 10.1021/Acs.Joc.7B00547 |
0.457 |
|
| 2017 |
Yu C, Zhang J, Zhong G. One step synthesis of γ-alkylidenebutenolides from simple vinyl carboxylic acids and alkenes. Chemical Communications (Cambridge, England). PMID 28828412 DOI: 10.1039/C7Cc04973K |
0.407 |
|
| 2017 |
Ding L, Yu C, Zhao Z, Li F, Zhang J, Zhong G. Facile Preparation of (2Z,4E)-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate. Journal of Visualized Experiments : Jove. PMID 28671649 DOI: 10.3791/55766 |
0.497 |
|
| 2017 |
Meng K, Zhang J, Li F, Lin Z, Zhang K, Zhong G. Amide Directed Cross-Coupling between Alkenes and Alkynes: A Regio- and Stereoselective Approach to Substituted (2Z,4Z)-Dienamides. Organic Letters. PMID 28481556 DOI: 10.1021/Acs.Orglett.7B00695 |
0.399 |
|
| 2017 |
Zhang J, Lu X, Li T, Wang S, Zhong G. Copper-catalyzed oxidative cyclization of 2-amino-azaarenes with lignin models: synthesis of 3-phenoxy imidazo heterocycles. The Journal of Organic Chemistry. PMID 28429945 DOI: 10.1021/Acs.Joc.7B00480 |
0.437 |
|
| 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 |
0.419 |
|
| 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 |
0.461 |
|
| 2017 |
Li F, Yu C, Zhang J, Zhong G. Weinreb amide directed cross-coupling reaction between electron-deficient alkenes catalyzed by a rhodium catalyst. Organic & Biomolecular Chemistry. PMID 28098326 DOI: 10.1039/C7Ob00026J |
0.443 |
|
| 2017 |
Zhu L, Yan P, Zhang L, Chen Z, Zeng X, Zhong G. TiCl4/DMAP mediated Z-selective knovenagel condensation of isatins with nitroacetates and related compounds Rsc Advances. 7: 51352-51358. DOI: 10.1039/C7Ra09951G |
0.332 |
|
| 2016 |
Yu C, Li F, Zhang J, Zhong G. A direct cross-coupling reaction of electron-deficient alkenes using an oxidizing directing group. Chemical Communications (Cambridge, England). PMID 27966727 DOI: 10.1039/C6Cc07064G |
0.399 |
|
| 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 |
0.417 |
|
| 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 |
0.455 |
|
| 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 |
0.473 |
|
| 2016 |
Li F, Shen C, Zhang J, Wu L, Zhuo X, Ding L, Zhong G. Ruthenium(II)-Catalyzed Oxidant-Free C-H Olefination of Aromatic Carboxamides with Allyl Acetate Advanced Synthesis & Catalysis. 358: 3932-3937. DOI: 10.1002/Adsc.201600569 |
0.46 |
|
| 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 |
0.413 |
|
| 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 |
0.438 |
|
| 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 |
0.507 |
|
| 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 |
0.475 |
|
| 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 |
0.506 |
|
| 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 |
0.458 |
|
| 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 |
0.3 |
|
| 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 |
0.482 |
|
| 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 |
0.535 |
|
| 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 |
0.411 |
|
| 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 |
0.53 |
|
| 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 |
0.464 |
|
| 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 |
0.503 |
|
| 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 |
0.544 |
|
| 2012 |
Shi Z, Yu P, Loh T, Zhong G. Inside Back Cover: Catalytic Asymmetric [4+2] Annulation Initiated by an Aza-Rauhut-Currier Reaction: Facile Entry to Highly Functionalized Tetrahydropyridines (Angew. Chem. Int. Ed. 31/2012) Angewandte Chemie International Edition. 51: 7861-7861. DOI: 10.1002/Anie.201205173 |
0.468 |
|
| 2012 |
Shi Z, Yu P, Loh T, Zhong G. Innenrücktitelbild: Catalytic Asymmetric [4+2] Annulation Initiated by an Aza-Rauhut-Currier Reaction: Facile Entry to Highly Functionalized Tetrahydropyridines (Angew. Chem. 31/2012) Angewandte Chemie. 124: 7983-7983. DOI: 10.1002/Ange.201205173 |
0.487 |
|
| 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 |
0.485 |
|
| 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 |
0.469 |
|
| 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 |
0.637 |
|
| 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 |
0.391 |
|
| 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 |
0.534 |
|
| 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 |
0.562 |
|
| 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 |
0.525 |
|
| 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 |
0.564 |
|
| 2010 |
Zeng X, Ye K, Lu M, Chua PJ, Tan B, Zhong G. ChemInform Abstract: Chiral Broensted Acid Catalyzed Enantioselective Addition of α-Isocyanoacetamides to Aldehydes. Cheminform. 41: no-no. DOI: 10.1002/chin.201040123 |
0.3 |
|
| 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 |
0.396 |
|
| 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 |
0.448 |
|
| 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 |
0.567 |
|
| 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 |
0.568 |
|
| 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 |
0.574 |
|
| 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 |
0.461 |
|
| 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 |
0.492 |
|
| 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 |
0.55 |
|
| 2009 |
Zhu D, Lu M, Dai L, Zhong G. One-Pot Synthesis of Bicyclic Isoxazolidines with Five StereogenicCenters Synfacts. 2009: 1034-1034. DOI: 10.1055/S-0029-1217794 |
0.4 |
|
| 2009 |
Zeng X, Xu Z, Lu M, Zhong G. Enantioselective Aziridination Using Chiral Phosphoric Acids Synfacts. 2009: 1035-1035. DOI: 10.1055/S-0029-1217787 |
0.366 |
|
| 2009 |
Tan B, Zeng X, Lu Y, Chua PJ, Zhong G. A New Pyrrolidine-Based Catalyst for Nitro-Michael Additions Synfacts. 2009: 674-674. DOI: 10.1055/S-0029-1216774 |
0.35 |
|
| 2009 |
Lu M, Zhu D, Lu Y, Zeng X, Tan B, Xu Z, Zhong G. Brønsted Acid Catalyzed α-Hydroxylationof β-Dicarbonyl Compounds Synfacts. 2009: 685-685. DOI: 10.1055/S-0029-1216766 |
0.306 |
|
| 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 |
0.432 |
|
| 2009 |
Tan B, Shi Z, Chua PJ, Li Y, Zhong G. Synthesis of N-HydroxypyrrolesUsing N-Selective Nucleophilicity of Oximes Synfacts. 2009: 373-373. DOI: 10.1055/S-0028-1087889 |
0.301 |
|
| 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 |
0.528 |
|
| 2009 |
Chua PJ, Tan B, Zhong G. ChemInform Abstract: Highly Enantioselective L-Thiaproline Catalyzed α-Aminoxylation of Aldehydes in Aqueous Media. Cheminform. 40. DOI: 10.1002/chin.200934059 |
0.442 |
|
| 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 |
0.432 |
|
| 2008 |
Lu M, Zhu D, Lu Y, Hou Y, Tan B, Zhong G. Organocatalytic Asymmetric α‐Aminoxylation/Aza‐Michael Reactions for the Synthesis of Functionalized Tetrahydro‐1,2‐oxazines Angewandte Chemie. 47: 10013-10013. PMID 19072787 DOI: 10.1002/Anie.200890274 |
0.597 |
|
| 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 |
0.499 |
|
| 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 |
0.61 |
|
| 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 |
0.609 |
|
| 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 |
0.63 |
|
| 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 |
0.648 |
|
| 2008 |
Tan B, Chua PJ, Zeng X, Zhong G. Multisubstituted Cyclopentanes by the Domino Michael-HenryReaction Synfacts. 2008: 1103-1103. DOI: 10.1055/S-2008-1078148 |
0.469 |
|
| 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 |
0.366 |
|
| 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 |
0.671 |
|
| 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 |
0.449 |
|
| 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 |
0.527 |
|
| 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 |
0.508 |
|
| 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 |
0.639 |
|
| 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 |
0.365 |
|
| 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 |
0.415 |
|
| 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 |
0.517 |
|
| 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 |
0.71 |
|
| 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 |
0.565 |
|
| 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 |
0.754 |
|
| 1999 |
Zhong G, Lerner R, Barbas C. Erweiterung des Repertoires von katalytischen Antikörpern mit Aldolaseaktivität durch Kombination von reaktiver Immunisierung und Übergangszustandstheorie: neue Enantio- und Diastereoselektivitäten Angewandte Chemie. 111: 3957-3960. DOI: 10.1002/(Sici)1521-3757(19991216)111:24<3957::Aid-Ange3957>3.0.Co;2-H |
0.413 |
|
| 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 |
0.752 |
|
| 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 |
0.733 |
|
| 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 |
0.693 |
|
| 1998 |
Zhong G, Shabat D, List B, Anderson J, Sinha SC, Lerner RA, Barbas CF. Katalytische enantioselektive Retro-Aldolreaktion: kinetische Racematspaltung von β-Hydroxyketonen durch Aldolase-Antikörper Angewandte Chemie. 110: 2609-2612. DOI: 10.1002/(Sici)1521-3757(19980918)110:18<2609::Aid-Ange2609>3.0.Co;2-E |
0.66 |
|
| 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 |
0.592 |
|
| 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 |
0.536 |
|
| 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 |
0.579 |
|
| Show low-probability matches. |