| Year |
Citation |
Score |
| 2024 |
Chen KL, Tanaka F. Organocatalytic enantioselective Mannich and retro-Mannich reactions and combinations of these reactions to afford tetrasubstituted α-amino acid derivatives. Organic & Biomolecular Chemistry. 22: 477-481. PMID 38099926 DOI: 10.1039/d3ob01855e |
0.393 |
|
| 2023 |
Garg Y, Osborne J, Vasylevskyi S, Velmurugan N, Tanaka F. 1,3-Diamine-Derived Catalysts: Design, Synthesis, and the Use in Enantioselective Mannich Reactions of Ketones. The Journal of Organic Chemistry. PMID 37460110 DOI: 10.1021/acs.joc.3c01051 |
0.456 |
|
| 2023 |
Sohail M, Tanaka F. Limiting the Loading of Reactant 1,3-Cyclohexanedione Enables the Use of Less Catalyst. The Journal of Organic Chemistry. PMID 37403968 DOI: 10.1021/acs.joc.3c00838 |
0.372 |
|
| 2022 |
Tanaka F. Amines as Catalysts: Dynamic Features and Kinetic Control of Catalytic Asymmetric Chemical Transformations to Form C-C Bonds and Complex Molecules. Chemical Record (New York, N.Y.). e202200207. PMID 36202628 DOI: 10.1002/tcr.202200207 |
0.355 |
|
| 2022 |
Aher RD, Ishikawa A, Yamanaka M, Tanaka F. Catalytic Enantioselective Construction of Decalin Derivatives by Dynamic Kinetic Desymmetrization of C2-Symmetric Derivatives through Aldol-Aldol Annulation. The Journal of Organic Chemistry. 87: 8151-8157. PMID 35666096 DOI: 10.1021/acs.joc.2c00889 |
0.412 |
|
| 2022 |
Mondal S, Aher RD, Bethi V, Lin YJ, Taniguchi T, Monde K, Tanaka F. Control of Reactions of Pyruvates by Catalysts: Direct Enantioselective Mannich Reactions of Pyruvates Catalyzed by Amine-based Catalyst Systems. Organic Letters. PMID 35226512 DOI: 10.1021/acs.orglett.2c00436 |
0.737 |
|
| 2021 |
Fujioka T, Numoto N, Akama H, Shilpa K, Oka M, Roy PK, Krishna Y, Ito N, Baker D, Oda M, Tanaka F. Varying the Directionality of Protein Catalysts for Aldol and Retro-aldol Reactions. Chembiochem : a European Journal of Chemical Biology. PMID 34698422 DOI: 10.1002/cbic.202100435 |
0.387 |
|
| 2021 |
Pasha M, Tanaka F. Organocatalytic diastereo- and enantioselective oxa-hetero-Diels-Alder reactions of enones with aryl trifluoromethyl ketones for the synthesis of trifluoromethyl-substituted tetrahydropyrans. Organic & Biomolecular Chemistry. 19: 9242-9250. PMID 34661230 DOI: 10.1039/d1ob01844b |
0.457 |
|
| 2021 |
Tanaka F, Sohail M. Dynamic Kinetic Asymmetric Transformation of Racemic Diastereomers: Diastereo- and Enantioconvergent Michael-Henry Reactions to Afford Spirooxindoles Bearing Furan-Fused Rings. Angewandte Chemie (International Ed. in English). PMID 34236757 DOI: 10.1002/anie.202108734 |
0.379 |
|
| 2021 |
Krishna Y, Tanaka F. Intramolecular Formal [4 + 2] Cycloadditions: Synthesis of Spiro Isoindolinone Derivatives and Related Molecules. Organic Letters. PMID 33601884 DOI: 10.1021/acs.orglett.1c00283 |
0.348 |
|
| 2020 |
Garg Y, Tanaka F. Enantioselective Direct -Selective Mannich-type Reactions Catalyzed by 3-Pyrrolidinecarboxylic Acid in the Presence of Potassium Carbonate: Addition of Potassium Carbonate Improves Enantioselectivities. Organic Letters. PMID 32428413 DOI: 10.1021/Acs.Orglett.0C01561 |
0.538 |
|
| 2020 |
Maram L, Tanaka F. Switching Electrophile Intermediates to Nucleophiles: Michael and Oxa-Diels-Alder Reactions to Afford Polyoxy-Functionalized Piperidine Derivatives with Tetrasubstituted Carbon. Organic Letters. PMID 32193936 DOI: 10.1021/Acs.Orglett.0C00735 |
0.439 |
|
| 2020 |
Tanaka F, Pasha M, Sohail M. Intramolecular Oxa-Michael Reactions of Aldols Generated from Enones and Isatins to Afford Spirooxindole Tetrahydropyrans Heterocycles. 101: 339. DOI: 10.3987/Com-19-S(F)26 |
0.512 |
|
| 2019 |
Zhang D, Chen Y, Cai H, Yin L, Zhong J, Man J, Zhang QF, Bethi V, Tanaka F. Direct Catalytic Asymmetric Synthesis of Oxindole-Derived δ-Hydroxy-β-ketoesters by Aldol Reactions. Organic Letters. PMID 31746616 DOI: 10.1021/Acs.Orglett.9B03527 |
0.484 |
|
| 2019 |
Sohail M, Tanaka F. Control of Chemical Reactions Using Molecules that Buffer Non-aqueous Solutions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31646678 DOI: 10.1002/Chem.201903552 |
0.407 |
|
| 2019 |
Krishna Y, Shilpa K, Tanaka F. Intramolecular Mannich and Michael Annulation Reactions of Lactam Derivatives Bearing Enals To Afford Bicyclic N-Heterocycles. Organic Letters. PMID 31584286 DOI: 10.1021/Acs.Orglett.9B03210 |
0.489 |
|
| 2019 |
Maram L, Tanaka F. Mannich Reactions of Carbohydrate Derivatives with Ketones To Afford Polyoxy-Functionalized Piperidines. Organic Letters. PMID 30693778 DOI: 10.1021/Acs.Orglett.9B00105 |
0.504 |
|
| 2019 |
Tanaka F, Enukonda J, Johnson S. C-Glycosidation of Unprotected Aldopentoses with Ketones Using Proline-Triethylamine as Catalyst Heterocycles. 99: 633. DOI: 10.3987/Com-18-S(F)13 |
0.336 |
|
| 2019 |
Sohail M, Tanaka F. Dynamic stereoselective annulation via aldol-oxa-cyclization cascade reaction to afford spirooxindole pyran polycycles Communications Chemistry. 2. DOI: 10.1038/s42004-019-0177-5 |
0.369 |
|
| 2019 |
Sohail M, Tanaka F. Cover Feature: Control of Chemical Reactions by Using Molecules that Buffer Non‐aqueous Solutions (Chem. Eur. J. 1/2020) Chemistry – a European Journal. 26: 4-4. DOI: 10.1002/Chem.201904861 |
0.347 |
|
| 2018 |
Chouthaiwale PV, Aher RD, Tanaka F. Catalytic Enantioselective Formal (4+2) Cycloaddition by Aldol-Aldol Annulation of Pyruvate Derivatives with Cyclohexane-1,3-Diones to Afford Functionalized Decalins. Angewandte Chemie (International Ed. in English). PMID 30125444 DOI: 10.1002/Anie.201808219 |
0.509 |
|
| 2018 |
Yin F, Garifullina A, Tanaka F. Correction: Synthesis of pyrrolidine-3-carboxylic acid derivatives via asymmetric Michael addition reactions of carboxylate-substituted enones. Organic & Biomolecular Chemistry. PMID 29651476 DOI: 10.1039/c8ob90051e |
0.357 |
|
| 2018 |
Johnson S, Bagdi AK, Tanaka F. C-Glycosidation of Unprotected Di- and Trisaccharide Aldopyranoses with Ketones Using Pyrrolidine-Boric Acid Catalysis. The Journal of Organic Chemistry. PMID 29595968 DOI: 10.1021/Acs.Joc.8B00340 |
0.353 |
|
| 2018 |
Tanaka F, V. Chouthaiwale P, D. Aher R. Reactions of Pyruvate-Derived Dihydropyrans with Formaldehyde: Synthesis of Functionalized Furopyrans and Related Products Heterocycles. 97: 569. DOI: 10.3987/Com-18-S(T)29 |
0.454 |
|
| 2018 |
Zhang D, Chuang P, Cao D, Krishna Y, Shilpa K, Tanaka F. Detection of enantiomers of chiral primary amines by 1H NMR analysis via enamine formation with an enantiopure γ-position aldol product of a β-keto ester Tetrahedron Letters. 59: 2248-2250. DOI: 10.1016/J.Tetlet.2018.04.079 |
0.352 |
|
| 2017 |
Yin F, Garifullina A, Tanaka F. Synthesis of pyrrolidine-3-carboxylic acid derivatives via asymmetric Michael addition reactions of carboxylate-substituted enones. Organic & Biomolecular Chemistry. PMID 28686271 DOI: 10.1039/C7Ob01484H |
0.513 |
|
| 2017 |
Zhang D, Tanaka F. Determination of Relative Frequency of Carbanion Formation at α-Positions of Ketones under Aldol Reaction Catalysis Conditions. Organic Letters. PMID 28671473 DOI: 10.1021/Acs.Orglett.7B01676 |
0.485 |
|
| 2017 |
Huang JR, Sohail M, Taniguchi T, Monde K, Tanaka F. Formal (4+1) Cycloaddition and Enantioselective Michael-Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles. Angewandte Chemie (International Ed. in English). PMID 28397989 DOI: 10.1002/Anie.201701049 |
0.49 |
|
| 2016 |
Kobayashi K, Ohshiro T, Tomoda H, Yin F, Cui HL, Chouthaiwale PV, Tanaka F. Discovery of SOAT2 inhibitors from synthetic small molecules. Bioorganic & Medicinal Chemistry Letters. PMID 27876317 DOI: 10.1016/J.Bmcl.2016.11.008 |
0.327 |
|
| 2016 |
Cui HL, Chouthaiwale PV, Yin F, Tanaka F. Catalytic asymmetric hetero-Diels-Alder reactions of enones with isatins to access functionalized spirooxindole tetrahydropyrans: scope, derivatization, and discovery of bioactives. Organic & Biomolecular Chemistry. PMID 26750767 DOI: 10.1039/C5Ob02393A |
0.503 |
|
| 2016 |
Zhang D, Tanaka F. Catalytic enantioselective oxa-hetero-Diels–Alder reactions of enones with aryl trifluoromethyl ketones Rsc Advances. 6: 61454-61457. DOI: 10.1039/C6Ra13859D |
0.535 |
|
| 2016 |
Cui HL, Chouthaiwale PV, Yin F, Tanaka F. Reaction-Based Mechanistic Investigations of Asymmetric Hetero-Diels-Alder Reactions of Enones with Isatins Catalyzed by Amine-Based Three-Component Catalyst Systems Asian Journal of Organic Chemistry. 5: 153-161. DOI: 10.1002/Ajoc.201500412 |
0.515 |
|
| 2015 |
Johnson S, Tanaka F. Direct synthesis of C-glycosides from unprotected 2-N-acyl-aldohexoses via aldol condensation-oxa-Michael reactions with unactivated ketones. Organic & Biomolecular Chemistry. PMID 26565955 DOI: 10.1039/C5Ob02094H |
0.391 |
|
| 2015 |
Jithender E, Katsuyama I, Zhang D, Johnson S, Tanaka F. Aldol reactions of 1,2-diketones catalyzed by amines to afford furanose derivatives Tetrahedron Letters. 56: 735-738. DOI: 10.1016/J.Tetlet.2014.12.094 |
0.537 |
|
| 2015 |
Cui H, Chouthaiwale PV, Yin F, Tanaka F. Inside Cover: Reaction-Based Mechanistic Investigations of Asymmetric Hetero-Diels-Alder Reactions of Enones with Isatins Catalyzed by Amine-Based Three-Component Catalyst Systems (Asian J. Org. Chem. 1/2016) Asian Journal of Organic Chemistry. 5: 2-2. DOI: 10.1002/Ajoc.201500503 |
0.511 |
|
| 2015 |
Zhang D, Tanaka F. Aldol Reactions of Ketone Donors with Aryl Trifluoromethyl Ketone Acceptors Catalyzed by 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) for Concise Access to Aryl- and Trifluoromethyl- Substituted Tertiary Alcohols Advanced Synthesis and Catalysis. 357: 3458-3462. DOI: 10.1002/Adsc.201500497 |
0.482 |
|
| 2014 |
Chouthaiwale PV, Tanaka F. Reactions of pyruvates: organocatalytic synthesis of functionalized dihydropyrans in one pot and further transformations to functionalized carbocycles and heterocycles. Chemical Communications (Cambridge, England). 50: 14881-4. PMID 25325901 DOI: 10.1039/C4Cc06035K |
0.446 |
|
| 2014 |
Cui HL, Tanaka F. One-pot synthesis of polysubstituted 3-acylpyrroles by cooperative catalysis. Organic & Biomolecular Chemistry. 12: 5822-6. PMID 24972009 DOI: 10.1039/C4Ob01019A |
0.398 |
|
| 2014 |
Mase N, Ando T, Shibagaki F, Sugita A, Narumi T, Toda M, Watanabe N, Tanaka F. Fluorogenic aldehydes bearing arylethynyl groups: Turn-on aldol reaction sensors for evaluation of organocatalysis in DMSO Tetrahedron Letters. 55: 1946-1948. DOI: 10.1016/J.Tetlet.2014.02.007 |
0.69 |
|
| 2014 |
Katsuyama I, Chouthaiwale PV, Akama H, Cui HL, Tanaka F. Fluorogenic probes for aldol reactions: Tuning of fluorescence using π-conjugation systems Tetrahedron Letters. 55: 74-78. DOI: 10.1016/J.Tetlet.2013.10.122 |
0.494 |
|
| 2014 |
Zhang D, Johnson S, Cui HL, Tanaka F. Synthesis of furanose spirooxindoles via 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)-catalyzed aldol reactions of a pyruvic aldehyde derivative Asian Journal of Organic Chemistry. 3: 391-394. DOI: 10.1002/Ajoc.201400016 |
0.479 |
|
| 2013 |
Cui HL, Tanaka F. Catalytic enantioselective formal hetero-Diels-Alder reactions of enones with isatins to give spirooxindole tetrahydropyranones. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 6213-6. PMID 23559482 DOI: 10.1002/Chem.201300595 |
0.492 |
|
| 2013 |
Mase N, Takabe K, Tanaka F. Erratum to “Fluorogenic probes for chemical transformations: 9-anthracene derivatives for monitoring reaction progress by an increase in fluorescence” [Tetrahedron Lett. 54 (2013) 4306–4308] Tetrahedron Letters. 54: 5140. DOI: 10.1016/J.Tetlet.2013.07.086 |
0.642 |
|
| 2013 |
Mase N, Takabe K, Tanaka F. Fluorogenic probes for chemical transformations: 9-anthracene derivatives for monitoring reaction progress by an increase in fluorescence Tetrahedron Letters. 54: 4306-4308. DOI: 10.1016/J.Tetlet.2013.06.010 |
0.657 |
|
| 2013 |
Katsuyama I, Chouthaiwale PV, Cui HL, Ito Y, Sando A, Tokiwa H, Tanaka F. Substituent-dependent reactivity in aldehyde transformations: 4-(phenylethynyl)benzaldehydes versus simple benzaldehydes Tetrahedron. 69: 4098-4104. DOI: 10.1016/J.Tet.2013.03.056 |
0.487 |
|
| 2009 |
Zhu X, Tanaka F, Lerner RA, Barbas CF, Wilson IA. Direct observation of an enamine intermediate in amine catalysis. Journal of the American Chemical Society. 131: 18206-7. PMID 19968282 DOI: 10.1021/Ja907271A |
0.571 |
|
| 2009 |
Guo HM, Tanaka F. A fluorogenic aldehyde bearing a 1,2,3-triazole moiety for monitoring the progress of aldol reactions. The Journal of Organic Chemistry. 74: 2417-24. PMID 19222210 DOI: 10.1021/Jo900013W |
0.502 |
|
| 2009 |
Tanaka F. Enamine-Based Reactions: Strategies for the Development of Organocatalysts and Catalyzed Reactions Journal of the Society of Japanese Women Scientists. 10: 1-9. DOI: 10.5939/sjws.09001 |
0.408 |
|
| 2008 |
Minakawa M, Guo HM, Tanaka F. Imines that react with phenols in water over a wide pH range. The Journal of Organic Chemistry. 73: 8669-72. PMID 18844415 DOI: 10.1021/Jo8017389 |
0.339 |
|
| 2008 |
Tanaka F, Hu Y, Sutton J, Asawapornmongkol L, Fuller R, Olson AJ, Barbas CF, Lerner RA. Selection of phage-displayed peptides that bind to a particular ligand-bound antibody. Bioorganic & Medicinal Chemistry. 16: 5926-31. PMID 18472269 DOI: 10.1016/J.Bmc.2008.04.062 |
0.476 |
|
| 2008 |
Guo HM, Minakawa M, Tanaka F. Fluorogenic imines for fluorescent detection of Mannich-type reactions of phenols in water. The Journal of Organic Chemistry. 73: 3964-6. PMID 18429632 DOI: 10.1021/Jo8003293 |
0.414 |
|
| 2008 |
Jiang L, Althoff EA, Clemente FR, Doyle L, Röthlisberger D, Zanghellini A, Gallaher JL, Betker JL, Tanaka F, Barbas CF, Hilvert D, Houk KN, Stoddard BL, Baker D. De novo computational design of retro-aldol enzymes. Science (New York, N.Y.). 319: 1387-91. PMID 18323453 DOI: 10.1126/Science.1152692 |
0.328 |
|
| 2008 |
Zhang H, Mitsumori S, Utsumi N, Imai M, Garcia-Delgado N, Mifsud M, Albertshofer K, Cheong PH, Houk KN, Tanaka F, Barbas CF. Catalysis of 3-pyrrolidinecarboxylic acid and related pyrrolidine derivatives in enantioselective anti-Mannich-type reactions: importance of the 3-acid group on pyrrolidine for stereocontrol. Journal of the American Chemical Society. 130: 875-86. PMID 18163619 DOI: 10.1021/Ja074907+ |
0.5 |
|
| 2008 |
Zhang H, Ramasastry SSV, Tanaka F, Barbas CF. Organocatalytic anti-Mannich reactions with dihydroxyacetone and acyclic dihydroxyacetone derivatives: A facile route to amino sugars Advanced Synthesis and Catalysis. 350: 791-796. DOI: 10.1002/Adsc.200800069 |
0.728 |
|
| 2007 |
Hayashi I, Mizuno H, Tong KI, Furuta T, Tanaka F, Yoshimura M, Miyawaki A, Ikura M. Crystallographic evidence for water-assisted photo-induced peptide cleavage in the stony coral fluorescent protein Kaede. Journal of Molecular Biology. 372: 918-26. PMID 17692334 DOI: 10.1016/J.Jmb.2007.06.037 |
0.338 |
|
| 2007 |
Utsumi N, Imai M, Tanaka F, Ramasastry SS, Barbas CF. Mimicking aldolases through organocatalysis: syn-selective aldol reactions with protected dihydroxyacetone. Organic Letters. 9: 3445-8. PMID 17645352 DOI: 10.1021/Ol701467S |
0.737 |
|
| 2007 |
Ramasastry SS, Albertshofer K, Utsumi N, Tanaka F, Barbas CF. Mimicking fructose and rhamnulose aldolases: organocatalytic syn-aldol reactions with unprotected dihydroxyacetone. Angewandte Chemie (International Ed. in English). 46: 5572-5. PMID 17577894 DOI: 10.1002/Anie.200701269 |
0.728 |
|
| 2007 |
Tanaka F, Jones T, Kubitz D, Lerner RA. Anti-formyl peptide antibodies. Bioorganic & Medicinal Chemistry Letters. 17: 1943-5. PMID 17293112 DOI: 10.1016/J.Bmcl.2007.01.082 |
0.472 |
|
| 2007 |
Ramasastry SS, Zhang H, Tanaka F, Barbas CF. Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactions. Journal of the American Chemical Society. 129: 288-9. PMID 17212404 DOI: 10.1021/Ja0677012 |
0.713 |
|
| 2007 |
Utsumi N, Imai M, Tanaka F, Ramasastry SSV, Barbas CF. syn-Selective Organocatalytic Aldol Reactions of Dihydroxyacetone Equivalents Synfacts. 2007: 1100-1100. DOI: 10.1055/S-2007-969002 |
0.488 |
|
| 2007 |
III C, Ramasastry S, Zhang H, Tanaka F. Organocatalytic anti-Mannich and syn-Aldol Reactions of α-Hydroxy Ketones Synfacts. 2007: 0325-0325. DOI: 10.1055/S-2007-968235 |
0.705 |
|
| 2007 |
Albertshofer K, Thayumanavan R, Utsumi N, Tanaka F, Barbas CF. Amine-catalyzed Michael reactions of an aminoaldehyde derivative to nitroolefins Tetrahedron Letters. 48: 693-696. DOI: 10.1016/J.Tetlet.2006.11.096 |
0.497 |
|
| 2007 |
Tanaka F, Barbas CF. Enamine Catalysis: Aldol and Mannich-Type Reactions Enantioselective Organocatalysis: Reactions and Experimental Procedures. 19-55. DOI: 10.1002/9783527610945.ch2a |
0.369 |
|
| 2006 |
Zhang H, Mifsud M, Tanaka F, Barbas CF. 3-Pyrrolidinecarboxylic acid for direct catalytic asymmetric anti-Mannich-type reactions of unmodified ketones. Journal of the American Chemical Society. 128: 9630-1. PMID 16866507 DOI: 10.1021/ja062950b |
0.451 |
|
| 2006 |
Chowdari NS, Ahmad M, Albertshofer K, Tanaka F, Barbas CF. Expedient synthesis of chiral 1,2- and 1,4-diamines: protecting group dependent regioselectivity in direct organocatalytic asymmetric Mannich reactions. Organic Letters. 8: 2839-42. PMID 16774270 DOI: 10.1021/ol060980d |
0.459 |
|
| 2006 |
Suri JT, Mitsumori S, Albertshofer K, Tanaka F, Barbas CF. Dihydroxyacetone variants in the organocatalytic construction of carbohydrates: mimicking tagatose and fuculose aldolases. The Journal of Organic Chemistry. 71: 3822-8. PMID 16674055 DOI: 10.1021/Jo0602017 |
0.768 |
|
| 2006 |
Mase N, Watanabe K, Yoda H, Takabe K, Tanaka F, Barbas CF. Organocatalytic direct michael reaction of ketones and aldehydes with beta-nitrostyrene in brine. Journal of the American Chemical Society. 128: 4966-7. PMID 16608326 DOI: 10.1021/Ja060338E |
0.71 |
|
| 2006 |
Cheong PH, Zhang H, Thayumanavan R, Tanaka F, Houk KN, Barbas CF. Pipecolic acid-catalyzed direct asymmetric mannich reactions. Organic Letters. 8: 811-4. PMID 16494447 DOI: 10.1021/Ol052861O |
0.49 |
|
| 2006 |
Mitsumori S, Zhang H, Cheong PHY, Houk KN, Tanaka F, Barbas CF. Direct asymmetric anti-Mannich-type reactions catalyzed by a designed amino acid Journal of the American Chemical Society. 128: 1040-1041. PMID 16433496 DOI: 10.1021/Ja056984F |
0.544 |
|
| 2006 |
Mase N, Nakai Y, Ohara N, Yoda H, Takabe K, Tanaka F, Barbas CF. Organocatalytic direct asymmetric aldol reactions in water. Journal of the American Chemical Society. 128: 734-5. PMID 16417359 DOI: 10.1021/Ja0573312 |
0.695 |
|
| 2006 |
Tanaka F, Barbas, III C, Zhang H, Mifsud M. Organocatalytic anti-Mannich Reaction of Ketones Synfacts. 2006: 0956-0956. DOI: 10.1055/S-2006-949232 |
0.504 |
|
| 2005 |
Tanaka F. Development of protein, peptide, and small molecule catalysts using catalysis-based selection strategies. Chemical Record (New York, N.Y.). 5: 276-85. PMID 16211623 DOI: 10.1002/Tcr.20051 |
0.534 |
|
| 2005 |
Tanaka F, Fuller R, Barbas CF. Development of small designer aldolase enzymes: catalytic activity, folding, and substrate specificity. Biochemistry. 44: 7583-92. PMID 15896002 DOI: 10.1021/Bi050216J |
0.439 |
|
| 2005 |
Tanaka F, Barbas CF. Enamine-based Reactions Using Organocatalysts Journal of Synthetic Organic Chemistry Japan. 63: 709-721. DOI: 10.5059/Yukigoseikyokaishi.63.709 |
0.557 |
|
| 2005 |
Tanaka F, Barbas CF. Enamine-based reactions using organocatalysts: From aldolase antibodies to small amino acid and amine catalysts Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 63: 709-721. |
0.405 |
|
| 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 |
0.676 |
|
| 2004 |
Thayumanavan R, Tanaka F, Barbas III CF. Direct organocatalytic asymmetric aldol reactions of alpha-amino aldehydes: expedient syntheses of highly enantiomerically enriched anti-beta-hydroxy-alpha-amino acids. Organic Letters. 6: 3541-4. PMID 15387543 DOI: 10.1021/ol0485417 |
0.32 |
|
| 2004 |
Sinha SC, Li LS, Watanabe S, Kaltgrad E, Tanaka F, Rader C, Lerner RA, Barbas CF. Aldolase antibody activation of prodrugs of potent aldehyde-containing cytotoxics for selective chemotherapy. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 5467-72. PMID 15378729 DOI: 10.1002/Chem.200400419 |
0.603 |
|
| 2004 |
Notz W, Tanaka F, Barbas CF. Enamine-based organocatalysis with proline and diamines: the development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-alder reactions. Accounts of Chemical Research. 37: 580-91. PMID 15311957 DOI: 10.1021/Ar0300468 |
0.421 |
|
| 2004 |
Tanaka F, Mase N, Barbas CF. Determination of cysteine concentration by fluorescence increase: reaction of cysteine with a fluorogenic aldehyde. Chemical Communications (Cambridge, England). 1762-3. PMID 15278174 DOI: 10.1039/B405642F |
0.612 |
|
| 2004 |
Mase N, Thayumanavan R, Tanaka F, Barbas CF. Direct asymmetric organocatalytic Michael reactions of alpha,alpha-disubstituted aldehydes with beta-nitrostyrenes for the synthesis of quaternary carbon-containing products. Organic Letters. 6: 2527-30. PMID 15255682 DOI: 10.1021/Ol049196O |
0.663 |
|
| 2004 |
Tanaka F, Flores F, Kubitz D, Lerner RA, Barbas CF. Antibody-catalyzed aminolysis of a chloropyrimidine derivative. Chemical Communications (Cambridge, England). 1242-3. PMID 15136858 DOI: 10.1039/B403672G |
0.59 |
|
| 2004 |
Mase N, Tanaka F, Barbas CF. Synthesis of beta-hydroxyaldehydes with stereogenic quaternary carbon centers by direct organocatalytic asymmetric aldol reactions. Angewandte Chemie (International Ed. in English). 43: 2420-3. PMID 15114579 DOI: 10.1002/Anie.200353546 |
0.639 |
|
| 2004 |
Tanaka F, Mase N, Barbas CF. Design and use of fluorogenic aldehydes for monitoring the progress of aldehyde transformations. Journal of the American Chemical Society. 126: 3692-3. PMID 15038704 DOI: 10.1021/Ja049641A |
0.696 |
|
| 2004 |
Tanaka F, Fuller R, Shim H, Lerner RA, Barbas CF. Evolution of aldolase antibodies in vitro: correlation of catalytic activity and reaction-based selection. Journal of Molecular Biology. 335: 1007-18. PMID 14698295 DOI: 10.1016/J.Jmb.2003.11.014 |
0.672 |
|
| 2004 |
Betancort JM, Sakthivel K, Thayumanavan R, Tanaka F, Barbas CF. Catalytic direct asymmetric Michael reactions: Addition of unmodified ketone and aldehyde donors to alkylidene malonates and nitro olefins Synthesis. 1509-1521. DOI: 10.1055/S-2004-822392 |
0.552 |
|
| 2004 |
Tanaka F, Thayumanavan R, Mase N, Barbas CF. Rapid analysis of solvent effects on enamine formation by fluorescence: How might enzymes facilitate enamine chemistry with primary amines? Tetrahedron Letters. 45: 325-328. DOI: 10.1016/J.Tetlet.2003.10.157 |
0.655 |
|
| 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 |
0.629 |
|
| 2003 |
Notz W, Tanaka F, Watanabe S, Chowdari NS, Turner JM, Thayumanavan R, Barbas CF. The direct organocatalytic asymmetric mannich reaction: unmodified aldehydes as nucleophiles. The Journal of Organic Chemistry. 68: 9624-34. PMID 14656087 DOI: 10.1021/Jo0347359 |
0.507 |
|
| 2003 |
Mase N, Tanaka F, Barbas CF. Rapid fluorescent screening for bifunctional amine-acid catalysts: efficient syntheses of quaternary carbon-containing aldols under organocatalysis. Organic Letters. 5: 4369-72. PMID 14602002 DOI: 10.1021/ol035651p |
0.629 |
|
| 2003 |
Tanaka F, Thayumanavan R, Barbas CF. Fluorescent detection of carbon-carbon bond formation. Journal of the American Chemical Society. 125: 8523-8. PMID 12848558 DOI: 10.1021/Ja034069T |
0.44 |
|
| 2002 |
Tanaka F. Catalytic antibodies as designer proteases and esterases. Chemical Reviews. 102: 4885-906. PMID 12475210 DOI: 10.1021/Cr010180A |
0.33 |
|
| 2002 |
Watanabe S, Córdova A, Tanaka F, Barbas CF. One-pot asymmetric synthesis of beta-cyanohydroxymethyl alpha-amino acid derivatives: formation of three contiguous stereogenic centers. Organic Letters. 4: 4519-22. PMID 12465927 DOI: 10.1021/Ol027048X |
0.478 |
|
| 2002 |
Tanaka F, Barbas CF. Reactive immunization: a unique approach to catalytic antibodies. Journal of Immunological Methods. 269: 67-79. PMID 12379353 DOI: 10.1016/S0022-1759(02)00225-9 |
0.381 |
|
| 2002 |
Tanaka F, Barbas CF. A modular assembly strategy for improving the substrate specificity of small catalytic peptides. Journal of the American Chemical Society. 124: 3510-1. PMID 11929232 DOI: 10.1021/Ja0171815 |
0.334 |
|
| 2002 |
Córdova A, Watanabe S, Tanaka F, Notz W, Barbas CF. A highly enantioselective route to either enantiomer of both alpha- and beta-amino acid derivatives. Journal of the American Chemical Society. 124: 1866-7. PMID 11866595 DOI: 10.1021/Ja017833P |
0.446 |
|
| 2002 |
Thayumanavan R, Dhevalapally B, Sakthivel K, Tanaka F, Barbas CF. Amine-catalyzed direct Diels-Alder reactions of α,β-unsaturated ketones with nitro olefins Tetrahedron Letters. 43: 3817-3820. DOI: 10.1016/S0040-4039(02)00686-X |
0.533 |
|
| 2001 |
Tanaka F, Kerwin L, Kubitz D, Lerner RA, Barbas CF. Visualizing antibody-catalyzed retro-aldol-retro-Michael reactions. Bioorganic & Medicinal Chemistry Letters. 11: 2983-6. PMID 11677141 DOI: 10.1016/S0960-894X(01)00605-9 |
0.647 |
|
| 2001 |
Tanaka F, Barbas CF. Phage display selection of peptides possessing aldolase activity Chemical Communications. 769-770. DOI: 10.1039/B100479B |
0.374 |
|
| 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 |
0.717 |
|
| 2000 |
Tanaka F, Lerner RA, Barbas CF. Reconstructing aldolase antibodies to alter their substrate specificity and turnover Journal of the American Chemical Society. 122: 4835-4836. DOI: 10.1021/Ja0005441 |
0.494 |
|
| 1999 |
Tanaka F, Lerner RA, Barbas CF. Thiazolium-dependent catalytic antibodies produced using a covalent modification strategy Chemical Communications. 1383-1384. DOI: 10.1039/A902337B |
0.573 |
|
| 1999 |
Tanaka F, Almer H, Lerner RA, Barbas CF. Catalytic single-chain antibodies possessing β-lactamase activity selected from a phage displayed combinatorial library using a mechanism-based inhibitor Tetrahedron Letters. 40: 8063-8066. DOI: 10.1016/S0040-4039(99)01695-0 |
0.515 |
|
| 1998 |
Tanaka F, Oda M, Fujii I. Pyridoxal-mediated abzyme system for aldol and retro-aldol reactions Tetrahedron Letters. 39: 5057-5060. DOI: 10.1016/S0040-4039(98)00952-6 |
0.53 |
|
| 1996 |
Fujii I, Tanaka F, Miyashita H, Tanimura R, Kinoshita K. Transition state analysis within a panel of catalytic antibodies generated against a phosphonate transition state analog Phosphorus, Sulfur and Silicon and Related Elements. 109: 253-256. DOI: 10.1080/10426509608046246 |
0.314 |
|
| 1996 |
Tanaka F, Kinoshita K, Tanimura R, Fujii I. Relaxing substrate specificity in antibody-catalyzed reactions: Enantioselective hydrolysis of N-Cbz-amino acid esters Journal of the American Chemical Society. 118: 2332-2339. DOI: 10.1021/Ja952220W |
0.423 |
|
| 1995 |
Tanaka F, Node M, Tanaka K, Mizuchi M, Hosoi S, Nakayama M, Taga T, Fuji K. 1,1′-binaphthalene-2,2′-diol as a chiral auxiliary. Diastereoselective alkylation of binaphthyl esters, complex-induced proximity effects in enolate formation, and one-step synthesis of an optically active β-substituted ketone Journal of the American Chemical Society. 117: 12159-12171. DOI: 10.1021/Ja00154A016 |
0.548 |
|
| 1995 |
Fujii I, Tanaka F, Miyashita H, Tanimura R, Kinoshita K. Correlation between antigen-combining-site structures and functions within a panel of catalytic antibodies generated against a single transition state analog Journal of the American Chemical Society. 117: 6199-6209. DOI: 10.1021/Ja00128A006 |
0.308 |
|
| 1995 |
Okahata Y, Yamaguchi M, Tanaka F, Fujii I. A lipid-coated catalytic antibody in water-miscible organic solvents Tetrahedron. 51: 7673-7680. DOI: 10.1016/0040-4020(95)00407-Y |
0.327 |
|
| 1994 |
Miyashita H, Hara T, Tamimura R, Tanaka F, Kikuchi M, Fujii I. A common ancestry for multiple catalytic antibodies generated against a single transition-state analog Proceedings of the National Academy of Sciences of the United States of America. 91: 10757. PMID 7938025 DOI: 10.1073/Pnas.91.22.10757A |
0.359 |
|
| 1992 |
Tanaka F, Fuji K. Stereochemistry of the enolate from methyl phenylacetate Tetrahedron Letters. 33: 7885-7888. DOI: 10.1016/S0040-4039(00)74769-1 |
0.497 |
|
| 1991 |
Fujia K, Tanaka F, Node M. Binaphthol as a chiral auxilliary: diastereoselective alkylation of binaphthyl esters of α,β-unsaturated carboxylic acids Tetrahedron Letters. 32: 7281-7282. DOI: 10.1016/0040-4039(91)80498-U |
0.302 |
|
| 1990 |
Fuji K, Node M, Tanaka F. Complex-induced proximity effects in enolate formation. Highly diastereoselective α-methylation of binaphthyl esters of arylacetic acids Tetrahedron Letters. 31: 6553-6556. DOI: 10.1016/S0040-4039(00)97115-6 |
0.521 |
|
| 1989 |
Fuji K, Node M, Tanaka F, Hosoi S. Binaphthol as a chiral auxiliary. Asymmetrical alkylation of arylacetic acid Tetrahedron Letters. 30: 2825-2828. DOI: 10.1016/S0040-4039(00)99135-4 |
0.557 |
|
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