C. F. Iii Barbas
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Chemistry
C. F. Iii Barbas's Degrees
- PhD Chemistry University of California, Berkeley
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(Suggest an Edit or Addition)C. F. Iii Barbas's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Proline-Catalyzed Direct Asymmetric Aldol Reactions (2000) (1977)
- Enamine-based organocatalysis with proline and diamines: the development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-alder reactions. (2004) (1101)
- De Novo Computational Design of Retro-Aldol Enzymes (2008) (1011)
- Amino acid catalyzed direct asymmetric aldol reactions: a bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions. (2001) (918)
- Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies (2014) (626)
- Organocatalytic direct asymmetric aldol reactions in water. (2006) (530)
- Organocatalysis lost: modern chemistry, ancient chemistry, and an unseen biosynthetic apparatus. (2008) (419)
- Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst. (2011) (392)
- Catalytic direct asymmetric Michael reactions: taming naked aldehyde donors. (2001) (364)
- Core-structure-motivated design of a phosphine-catalyzed [3+2] cycloaddition reaction: enantioselective syntheses of spirocyclopenteneoxindoles. (2011) (357)
- Organocatalytic direct michael reaction of ketones and aldehydes with beta-nitrostyrene in brine. (2006) (352)
- Efficient Aldolase Catalytic Antibodies That Use the Enamine Mechanism of Natural Enzymes (1995) (352)
- Highly efficient hydrogen-bonding catalysis of the Diels-Alder reaction of 3-vinylindoles and methyleneindolinones provides carbazolespirooxindole skeletons. (2011) (300)
- A highly enantioselective amino acid-catalyzed route to functionalized α-amino acids (2002) (292)
- Thiourea-catalyzed highly enantio- and diastereoselective additions of oxindoles to nitroolefins: application to the formal synthesis of (+)-physostigmine. (2009) (289)
- Organocatalytic asymmetric domino knoevenagel/diels-alder reactions: a bioorganic approach to the diastereospecific and enantioselective construction of highly substituted spiro[5,5]undecane-1,5,9-triones. (2003) (289)
- Direct Asymmetric Organocatalytic Michael Reactions of α,α-Disubstituted Aldehydes with β-Nitrostyrenes for the Synthesis of Quaternary Carbon-Containing Products (2004) (264)
- Direct organocatalytic aldol reactions in buffered aqueous media. (2002) (254)
- Direct asymmetric alpha-fluorination of aldehydes. (2005) (247)
- Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactions. (2007) (243)
- A Highly Enantioselective Route to Either Enantiomer of Both α- and β-Amino Acid Derivatives (2002) (242)
- Direct asymmetric anti-Mannich-type reactions catalyzed by a designed amino acid. (2006) (233)
- Tyrosine bioconjugation through aqueous ene-type reactions: a click-like reaction for tyrosine. (2010) (216)
- Towards organo-click chemistry: development of organocatalytic multicomponent reactions through combinations of aldol, Wittig, Knoevenagel, Michael, Diels-Alder and Huisgen cycloaddition reactions. (2004) (210)
- A proline-catalyzed asymmetric Robinson annulation reaction (2000) (210)
- Catalytic enantioselective direct Michael additions of ketones to alkylidene malonates (2001) (208)
- The direct organocatalytic asymmetric mannich reaction: unmodified aldehydes as nucleophiles. (2003) (202)
- Proline-catalyzed one-step asymmetric synthesis of 5-hydroxy-(2E)-hexenal from acetaldehyde. (2002) (192)
- Determination of cysteine concentration by fluorescence increase: reaction of cysteine with a fluorogenic aldehyde. (2004) (185)
- Synthesis of beta-hydroxyaldehydes with stereogenic quaternary carbon centers by direct organocatalytic asymmetric aldol reactions. (2004) (180)
- In water, on water, and by water: mimicking nature's aldolases with organocatalysis and water. (2010) (175)
- Aldolase Antibodies of Remarkable Scope (1998) (165)
- Organocatalytic amidation and esterification of aldehydes with activating reagents by a cross-coupling strategy. (2012) (165)
- Amine-catalyzed direct asymmetric Mannich-type reactions (2001) (156)
- Use of a recombinant bacterial fructose-1,6-diphosphate aldolase in aldol reactions: preparative syntheses of 1-deoxynojirimycin, 1-deoxymannojirimycin, 1,4-dideoxy-1,4-imino-D-arabinitol, and fagomine (1989) (146)
- Direct organocatalytic asymmetric heterodomino reactions: the Knoevenagel/Diels-Alder/epimerization sequence for the highly diastereoselective synthesis of symmetrical and nonsymmetrical synthons of benzoannelated centropolyquinanes. (2004) (142)
- Enzyme Catalysis in Synthetic Carbohydrate Chemistry (1991) (138)
- Dimeric quinidine-catalyzed enantioselective aminooxygenation of oxindoles: an organocatalytic approach to 3-hydroxyoxindole derivatives. (2010) (135)
- Asymmetric Synthesis of Quaternary α- and β-Amino Acids and β-Lactams via Proline-Catalyzed Mannich Reactions with Branched Aldehyde Donors (2004) (134)
- Single-triggered trimeric prodrugs. (2005) (129)
- Facile and stabile linkages through tyrosine: bioconjugation strategies with the tyrosine-click reaction. (2013) (125)
- 3-Pyrrolidinecarboxylic acid for direct catalytic asymmetric anti-Mannich-type reactions of unmodified ketones. (2006) (124)
- Amine-catalyzed direct Diels-Alder reactions of α, β-unsaturated ketones with nitro olefins (2002) (124)
- Assembly of spirooxindole derivatives containing four consecutive stereocenters via organocatalytic Michael-Henry cascade reactions. (2012) (122)
- Mimicking dihydroxy acetone phosphate-utilizing aldolases through organocatalysis: a facile route to carbohydrates and aminosugars. (2005) (121)
- Total synthesis of LFA-1 antagonist BIRT-377 via organocatalytic asymmetric construction of a quaternary stereocenter. (2005) (118)
- Direct amino acid-catalyzed asymmetric desymmetrization of meso-compounds: tandem aminoxylation/O-N bond heterolysis reactions. (2005) (118)
- Prodrug activation gated by a molecular "OR" logic trigger. (2005) (117)
- 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. (2008) (115)
- Proline-catalyzed asymmetric assembly reactions: enzyme-like assembly of carbohydrates and polyketides from three aldehyde substrates (2002) (111)
- Water-compatible organocatalysts for direct asymmetric syn-aldol reactions of dihydroxyacetone and aldehydes. (2008) (111)
- Deoxyribose-5-phosphate aldolase as a synthetic catalyst (1990) (108)
- Direct Organocatalytic Asymmetric Aldol Reactions of α-Amino Aldehydes: Expedient Syntheses of Highly Enantiomerically Enriched anti-β-Hydroxy-α-amino Acids (2004) (107)
- Antibody-Catalyzed Enantioselective Robinson Annulation (1997) (106)
- Expanding the scope of cinchona alkaloid-catalyzed enantioselective alpha-aminations of oxindoles: a versatile approach to optically active 3-amino-2-oxindole derivatives. (2009) (105)
- Highly enantioselective organocatalytic α-amination reactions of aryl oxindoles: developing designer multifunctional alkaloid catalysts. (2010) (103)
- A way to highly enantiomerically enriched aza-Morita-Baylis-Hillman-type products. (2007) (101)
- Organocatalytic asymmetric assembly reactions: one-pot synthesis of functionalized beta-amino alcohols from aldehydes, ketones, and azodicarboxylates. (2003) (97)
- Core structure-based design of organocatalytic [3+2]-cycloaddition reactions: highly efficient and stereocontrolled syntheses of 3,3'-pyrrolidonyl spirooxindoles. (2012) (96)
- Dihydroxyacetone variants in the organocatalytic construction of carbohydrates: mimicking tagatose and fuculose aldolases. (2006) (96)
- Mimicking fructose and rhamnulose aldolases: organocatalytic syn-aldol reactions with unprotected dihydroxyacetone. (2007) (93)
- Molecular Computation of Solutions to Combinatorial Problems (2008) (93)
- Expedient synthesis of chiral 1,2- and 1,4-diamines: protecting group dependent regioselectivity in direct organocatalytic asymmetric Mannich reactions. (2006) (91)
- The Scope of the Direct Proline-Catalyzed Asymmetric Addition of Ketones to Imines (2004) (90)
- anti-Selective SMP-catalyzed direct asymmetric Mannich-type reactions: synthesis of functionalized amino acid derivatives (2002) (88)
- anti-Selective asymmetric Michael reactions of aldehydes and nitroolefins catalyzed by a primary amine/thiourea. (2009) (88)
- Organocatalytic enantioselective synthesis of metabotropic glutamate receptor ligands. (2005) (87)
- A search for peptide ligase: cosolvent-mediated conversion of proteases to esterases for irreversible synthesis of peptides (1988) (86)
- Towards organocatalytic polyketide synthases with diverse electrophile scope: trifluoroethyl thioesters as nucleophiles in organocatalytic Michael reactions and beyond. (2008) (83)
- Rapid fluorescent screening for bifunctional amine-acid catalysts: efficient syntheses of quaternary carbon-containing aldols under organocatalysis. (2003) (82)
- Amine-catalyzed direct self Diels–Alder reactions of α,β-unsaturated ketones in water: synthesis of pro-chiral cyclohexanones (2002) (82)
- Mimicking aldolases through organocatalysis: syn-selective aldol reactions with protected dihydroxyacetone. (2007) (80)
- Organocatalytic asymmetric assembly reactions for the syntheses of carbohydrate derivatives by intermolecular Michael-Henry reactions (2010) (78)
- Formylbenzene diazonium hexafluorophosphate reagent for tyrosine-selective modification of proteins and the introduction of a bioorthogonal aldehyde. (2012) (78)
- A Catalytic Enantioselective Route to Hydroxy-Substituted Quaternary Carbon Centers: Resolution of Tertiary Aldols with a Catalytic Antibody (1999) (75)
- Biochemical characterization and structural analysis of a highly proficient cocaine esterase. (2002) (70)
- Chemoenzymic Synthesis of Chiral Furan Derivatives: Useful Building Blocks for Optically Active Structures (1988) (69)
- Amino alcohol catalyzed direct asymmetric aldol reactions: enantioselective synthesis of anti-α-fluoro-β-hydroxy ketones (2004) (68)
- Pipecolic acid-catalyzed direct asymmetric mannich reactions. (2006) (68)
- Enantioselective Total Synthesis of Some Brevicomins Using Aldolase Antibody 38C2 (1998) (66)
- One-pot enantioselective syntheses of iminosugar derivatives using organocatalytic anti-michael-anti-aza-Henry reactions. (2010) (64)
- Highly enantio- and diastereoselective Mannich reactions of glycine Schiff bases with in situ generated N-Boc-imines catalyzed by a cinchona alkaloid thiourea. (2010) (63)
- Direct organocatalytic asymmetric Mannich-type reactions in aqueous media: one-pot Mannich-allylation reactions (2003) (62)
- Development of small designer aldolase enzymes: catalytic activity, folding, and substrate specificity. (2005) (61)
- Rapid analysis of solvent effects on enamine formation by fluorescence: how might enzymes facilitate enamine chemistry with primary amines? (2004) (61)
- Identification of a Region in the Integrin β3 Subunit That Confers Ligand Binding Specificity* (1997) (58)
- Direct observation of an enamine intermediate in amine catalysis. (2009) (58)
- Organocatalytic mannich-type reactions of trifluoroethyl thioesters. (2008) (56)
- The origin of enantioselectivity in aldolase antibodies: crystal structure, site-directed mutagenesis, and computational analysis. (2004) (54)
- Proline‐Catalyzed Direct Asymmetric Aldol Reactions. (2000) (52)
- Rationally designed amide donors for organocatalytic asymmetric Michael reactions. (2012) (48)
- Fluorescent detection of carbon-carbon bond formation. (2003) (47)
- Assembly of spirooxindole derivatives via organocatalytic iminium-enamine cascade reactions. (2012) (45)
- Reconstructing Aldolase Antibodies to Alter Their Substrate Specificity and Turnover (2000) (43)
- Phage display selection of peptides possessing aldolase activity (2001) (41)
- Asymmetric construction of spirocyclopentenebenzofuranone core structures via highly selective phosphine-catalyzed [3 + 2] cycloaddition reactions. (2013) (40)
- Copying Nature's Mechanism for the Decarboxylation of β-Keto Acids into Catalytic Antibodies by Reactive Immunization (1996) (40)
- Organocatalysis as a safe practical method for the stereospecific dibromination of unsaturated compounds. (2012) (37)
- A short enantioselective synthesis of 1-deoxy-l-xylulose by antibody catalysis (1999) (37)
- Design and use of fluorogenic aldehydes for monitoring the progress of aldehyde transformations. (2004) (34)
- One-Pot Asymmetric Synthesis of β-Cyanohydroxymethyl α-Amino Acid Derivatives: Formation of Three Contiguous Stereogenic Centers (2002) (33)
- A modular assembly strategy for improving the substrate specificity of small catalytic peptides. (2002) (33)
- Reactive immunization: a unique approach to catalytic antibodies. (2002) (32)
- Papain catalysed peptide synthesis: control of amidase activity and the introduction of unusual amino acids (1987) (30)
- Organocatalytic anti‐Mannich Reactions with Dihydroxyacetone and Acyclic Dihydroxyacetone Derivatives: A Facile Route to Amino Sugars (2008) (27)
- Amine-catalyzed Michael reactions of an aminoaldehyde derivative to nitroolefins (2007) (26)
- Catalytic single-chain antibodies possessing β-lactamase activity selected from a phage displayed combinatorial library using a mechanism-based inhibitor (1999) (25)
- Selective arylthiolane deprotection by singlet oxygen: a promising tool for sensors and prodrugs. (2015) (21)
- Enamine-Based Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and Diels—Alder Reactions (2004) (21)
- Organocatalysis in Ionic Liquids: Highly Efficient l-Proline-Catalyzed Direct Asymmetric Mannich Reactions Involving Ketone and Aldehyde Nucleophiles (2003) (18)
- Direct Asymmetric α‐Fluorination of Aldehydes. (2005) (17)
- Catalytic Direct Asymmetric Michael Reactions: Addition of Unmodified Ketone and Aldehyde Donors to Alkylidene Malonates and Nitro Olefins (2004) (17)
- Core-structure-motivated design of iminium-enolate organocascade reactions: enantioselective syntheses of 5,6-dihydroindolizines. (2013) (16)
- One-pot tripeptide syntheses from three single amino acid derivatives catalyzed by papain (1988) (16)
- Organocatalytic Direct Michael Reaction of Ketones and Aldehydes with β-Nitrostyrene in Brine. (2006) (16)
- Synthesis of β-Hydroxyaldehydes with Stereogenic Quaternary Carbon Centers by Direct Organocatalytic Asymmetric Aldol Reactions. (2004) (16)
- Antibody‐catalyzed Aldol Reactions (2008) (15)
- Thiazolium-dependent catalytic antibodies produced using a covalent modification strategy† (1999) (15)
- Enamine Catalysis: Aldol and Mannich‐Type Reactions (2007) (14)
- N-Tosylimidates in highly enantioselective organocatalytic Michael reactions (2009) (13)
- Use of a Recombinant Bacterial Fructose-1,6-diphosphate Aldolase in Aldol Reactions: Preparative Syntheses of 1-Deoxynojirimycin, 1-Deoxymannojirimycin, 1,4-Dideoxy-1,4-imino-D-arabinitol, and Fagomine. (1989) (12)
- COFACTOR-INDUCED REFINEMENT OF CATALYTIC ANTIBODY ACTIVITY : A METAL-SPECIFIC ALLOSTERIC EFFECT (1998) (12)
- The First Organocatalytic Hetero-Domino Knoevenagel-Diels-Alder-Epimerization Reactions: Diastereoselective Synthesis of Highly Substituted Spiro[cyclohexane-1,2′-indan]-1′,3′,4-triones (2003) (11)
- Highly Efficient Hydrogen-Bonding Catalysis of the Diels—Alder Reaction of 3-Vinylindoles and Methyleneindolinones Provides Carbazolespirooxindole Skeletons. (2012) (10)
- Antibody-catalyzed asymmetric intramolecular Michael addition of aldehydes and ketones to yield the disfavored cis-product. (2005) (8)
- Organocatalytic Asymmetric Assembly Reactions: One‐Pot Synthesis of Functionalized β‐Amino Alcohols from Aldehydes, Ketones, and Azodicarboxylates. (2003) (8)
- Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon—Carbon Bond‐Forming Reactions. (2010) (8)
- Thiourea‐Catalyzed Highly Enantio‐ and Diastereoselective Additions of Oxindoles to Nitroolefins: Application to the Formal Synthesis of (+)‐Physostigmine. (2009) (8)
- Overexpression and substrate specificity studies of phosphodeoxyribomutase and thymidine phosphorylase (1991) (7)
- Aldolase Antibodies of Remarkable Scope. (1998) (7)
- Direct Asymmetric Organocatalytic Michael Reactions of α,α-Disubstituted Aldehydes with β-Nitrostyrenes for the Synthesis of Quaternary Carbon-Containing Products. (2004) (6)
- Amine‐Catalyzed Direct Asymmetric Mannich‐Type Reactions. (2001) (6)
- A Proline‐Catalyzed Asymmetric Robinson Annulation Reaction. (2000) (6)
- Core Structure Based Design of Organocatalytic [3 + 2]‐Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′‐Pyrrolidonyl Spirooxindoles. (2012) (4)
- Reactive Immunization: A Unique Approach to Aldolase Antibodies (2005) (4)
- Enamine-based Reactions Using Organocatalysts (2005) (4)
- In vivo programming of endogenous antibodies via oral administration of adaptor ligands. (2017) (4)
- A Highly Enantioselective Amino Acid‐Catalyzed Route to Functionalized α‐Amino Acids. (2002) (4)
- A highly enantioselective route to either enantiomer of both alpha- and beta-amino acid derivatives. (2002) (4)
- Teaching Catalytic Antibodies to Undergraduate Students: An Organic Chemistry Lab Experiment (1999) (3)
- Selection of phage-displayed peptides that bind to a particular ligand-bound antibody. (2008) (3)
- Broadening the Aldolase Catalytic Antibody Repertoire by Combining Reactive Immunization and Transition State Theory: New Enantio‐ and Diastereoselectivities. (2000) (3)
- A Way to Highly Enantiomerically Enriched Aza‐Morita—Baylis—Hillman‐Type Products. (2007) (3)
- Aldol and Mannich‐Type Reactions (2013) (3)
- Organocatalysis in Ionic Liquids: Highly Efficient L-Proline-Catalyzed Direct Asymmetric Mannich Reactions Involving Ketone and Aldehyde Nucleophiles. (2004) (3)
- Mimicking Fructose and Rhamnulose Aldolases: Organocatalytic syn‐Aldol Reactions with Unprotected Dihydroxyacetone. (2007) (3)
- Core-Structure-Motivated Design of a Phosphine-Catalyzed [3 + 2] Cycloaddition Reaction: Enantioselective Syntheses of Spirocyclopenteneoxindoles. (2011) (3)
- syn-Selective Organocatalytic Aldol Reactions of Dihydroxyacetone Equivalents (2007) (2)
- Molecular Cloning of Aldolases for Synthetic Applications a (1990) (2)
- Assembly of Spirooxindole Derivatives Containing Four Consecutive Stereocenters via Organocatalytic Michael—Henry Cascade Reactions. (2012) (2)
- Cover Picture: Towards Organo‐Click Chemistry: Development of Organocatalytic Multicomponent Reactions Through Combinations of Aldol, Wittig, Knoevenagel, Michael, Diels–Alder and Huisgen Cycloaddition Reactions (Chem. Eur. J. 21/2004) (2004) (2)
- Practical enzymatic approaches to unusual peptides (1988) (2)
- Organocatalytic anti‐Mannich Reactions with Dihydroxyacetone and Acyclic Dihydroxyacetone Derivatives: A Facile Route to Amino Sugars. (2008) (2)
- Dimeric Quinidine‐Catalyzed Enantioselective Aminooxygenation of Oxindoles: An Organocatalytic Approach to 3‐Hydroxyoxindole Derivatives. (2010) (1)
- A highly enantioselective amino acid-catalyzed route to functionalized alpha-amino acids. (2002) (1)
- Chemoenzymic Synthesis of Chiral Furan Derivatives: Useful Building Blocks for Optically Active Structures. (1988) (1)
- A Search for Peptide Ligase: Cosolvent-Mediated Conversion of Proteases to Esterases for Irreversible Synthesis of Peptides. (1988) (1)
- Catalytic Direct Asymmetric Michael Reactions: Addition of Unmodified Ketone and Aldehyde Donors to Alkylidene Malonates and Nitro Olefins. (2004) (1)
- Enantioselective Total Synthesis of Some Brevicomins Using Aldolase Antibody 38C2. (1998) (1)
- Antibody-catalyzed aminolysis of a chloropyrimidine derivative. (2004) (1)
- Direct Amino Acid Catalyzed Asymmetric Desymmetrization of meso‐Compounds: Tandem Aminoxylation/O—N Bond Heterolysis Reactions. (2005) (1)
- A Short Enantioselective Synthesis of 1-Deoxy-L-xylulose by Antibody Catalysis. (1999) (1)
- Assembly of Spirooxindole Derivatives via Organocatalytic Iminium‐Enamine Cascade Reactions. (2013) (1)
- Direct asymmetric organocatalytic Michael reactions of alpha,alpha-disubstituted aldehydes with beta-nitrostyrenes for the synthesis of quaternary carbon-containing products. (2004) (1)
- Asymmetric Synthesis of Quaternary α‐ and β‐Amino Acids and β‐Lactams via Proline‐Catalyzed Mannich Reactions with Branched Aldehyde Donors. (2004) (1)
- Enamine-Based Reactions Using Organocatalysts: From Aldolase Antibodies to Small Amino Acid and Amine Catalysts (2005) (1)
- Expanding the Scope of Cinchona Alkaloid‐Catalyzed Enantioselective α‐Aminations of Oxindoles: A Versatile Approach to Optically Active 3‐Amino‐2‐oxindole Derivatives. (2010) (1)
- One‐Pot Enantioselective Syntheses of Iminosugar Derivatives Using Organocatalytic anti‐Michael—anti‐Aza‐Henry Reactions. (2011) (1)
- The First Organocatalytic Hetero‐Domino Knoevenagel—Diels—Alder‐Epimerization Reactions: Diastereoselective Synthesis of Highly Substituted Spiro[cyclohexane‐1,2′‐indan]‐1′,3′,4‐triones. (2004) (1)
- Catalytic Enantioselective Direct Michael Additions of Ketones to Alkylidene Malonates. (2001) (1)
- Organocatalytic Approaches to Enantioenriched β‐Amino Acids (2005) (1)
- Organocatalytic Direct Michael Reaction of Ketones and Aldehydes with β-Nitrostyrene in Brine [J. Am. Chem. Soc. 2006, 128, 4966−4967]. (2006) (1)
- One‐Pot Asymmetric Synthesis of β‐Cyanohydroxymethyl α‐Amino Acid Derivatives: Formation of Three Contiguous Stereogenic Centers. (2003) (1)
- One-pot asymmetric synthesis of beta-cyanohydroxymethyl alpha-amino acid derivatives: formation of three contiguous stereogenic centers. (2002) (1)
- ChemInform Abstract: Amine-Catalyzed Direct Diels-Alder Reactions of α,β-Unsaturated Ketones with Nitro Olefins. (2002) (1)
- CCDC 837893: Experimental Crystal Structure Determination (2011) (0)
- Organocatalytic anti-Mannich and syn-Aldol Reactions of α-Hydroxy Ketones (2007) (0)
- Organocatalytic Asymmetric Domino Knoevenagel/Diels—Alder Reactions: A Bioorganic Approach to the Diastereospecific and Enantioselective Construction of Highly Substituted Spiro[5,5]undecane-1,5,9-triones. (2003) (0)
- Organocatalytic anti-Mannich Reaction of Ketones (2006) (0)
- Total Synthesis of LFA‐1 Antagonist BIRT‐377 via Organocatalytic Asymmetric Construction of a Quaternary Stereocenter. (2005) (0)
- Direct Organocatalytic Asymmetric Mannich‐Type Reactions in Aqueous Media: One‐Pot Mannich‐Allylation Reactions. (2003) (0)
- A Highly Enantioselective Route to Either Enantiomer of Both α‐ and β‐Amino Acid Derivatives. (2002) (0)
- Synthesis of (S)-1-Amino-5-phosphonoindan-1-carboxylic Acid [(S)-APICA] (2006) (0)
- One-Pot Tripeptide Syntheses from Three Single Amino Acid Derivatives Catalyzed by Papain. (1988) (0)
- anti-Selective Michael Reactionof Aldehydes (2010) (0)
- Using the Process of Reactive Immunization to Induce Catalytic Antibodies with Complex Mechanisms: Aldolases (2010) (0)
- Tetrahedron Young Investigator Award 2009: Carlos F. Barbas, III. (2009) (0)
- Direct Organocatalytic Asymmetric Heterodomino Reactions: The Knoevenagel/Diels—Alder/Epimerization Sequence for the Highly Diastereoselective Synthesis of Symmetrical and Nonsymmetrical Synthons of Benzoanellated Centropolyquinanes. (2005) (0)
- Ser117Ala Mutant of Bacterial Cocaine Esterase cocE (2003) (0)
- Amine-Catalyzed Michael Reactions of an Aminoaldehyde Derivative to Nitroolefins. (2007) (0)
- Amino Alcohol Catalyzed Direct Asymmetric Aldol Reactions. Enantioselective Synthesis of anti‐α‐Fluoro‐β‐hydroxy Ketones. (2004) (0)
- Direct Organocatalytic Asymmetric Aldol Reactions of α-Amino Aldehydes: Expedient Syntheses of Highly Enantiomerically Enriched anti-β-Hydroxy-α-amino Acids. (2005) (0)
- Rapid Fluorescent Screening for Bifunctional Amine—Acid Catalysts: Efficient Syntheses of Quaternary Carbon-Containing Aldols under Organocatalysis. (2004) (0)
- A Catalytic Enantioselective Route to Hydroxy‐Substituted Quaternary Carbon Centers: Resolution of Tertiary Aldols with a Catalytic Antibody. (1999) (0)
- Structural studies of catalytic antibodies (1996) (0)
- Core‐Structure‐Motivated Design of Iminium—Enolate Organocascade Reactions: Enantioselective Syntheses of 5,6‐Dihydroindolizines. (2014) (0)
- Amine-Catalyzed Direct Self Diels—Alder Reactions of α,β-Unsaturated Ketones in Water: Synthesis of Pro-Chiral Cyclohexanones. (2002) (0)
- Proline‐Catalyzed Asymmetric Assembly Reactions: Enzyme‐Like Assembly of Carbohydrates and Polyketides from Three Aldehydes Substrates. (2003) (0)
- Catalytic Enantioselective Retro‐Aldol Reactions: Kinetic Resolution of β‐Hydroxyketones with Aldolase Antibodies. (1999) (0)
- anti-Selective SMP-Catalyzed Direct Asymmetric Mannich-Type Reactions: Synthesis of Functionalized Amino Acid Derivatives. (2003) (0)
- Tyr44Phe Mutant of Bacterial Cocaine Esterase cocE (2003) (0)
- Antibody‐Catalyzed Asymmetric Intramolecular Michael Addition of Aldehydes and Ketones to Yield the Disfavored cis‐Product. (2006) (0)
- Antibody-Catalyzed Asymmetric Intramolecular Michael Reaction (2006) (0)
- Aza-Morita-Baylis-Hillman-Type Products via Enamine Catalysis (2007) (0)
- Asymmetric synthesis of quaternary alpha- and beta-amino acids and beta-lactams via proline-catalyzed mannich reactions with branched aldehyde donors. (2004) (0)
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