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Organocatalysis Lost: Modern Chemistry, Ancient Chemistry, and an Unseen Biosynthetic Apparatus

Angewandte Chemie (International ed.), 2008, Vol.47 (1), p.42-47

Barbas, Carlos F. III

2008

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Cell-penetrating peptide-mediated delivery of TALEN proteins via bioconjugation for genome engineering

PloS one, 2014-01, Vol.9 (1), p.e85755

2014

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Rapid, Stable, Chemoselective Labeling of Thiols with Julia-Kocieński-like Reagents: A Serum-Stable Alternative to Maleimide-Based Protein Conjugation

Angewandte Chemie (International ed.), 2013-11, Vol.52 (48), p.12592-12596

2013

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Organocatalytic Amidation and Esterification of Aldehydes with Activating Reagents by a Cross-Coupling Strategy

Angewandte Chemie (International ed.), 2012-12, Vol.51 (50), p.12538-12541

International ed. in English, 2012

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Core-Structure-Motivated Design of a Phosphine-Catalyzed [3 + 2] Cycloaddition Reaction: Enantioselective Syntheses of Spirocyclopenteneoxindoles

Journal of the American Chemical Society, 2011-04, Vol.133 (13), p.4672-4675

2011

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Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst

Nature chemistry, 2011-06, Vol.3 (6), p.473

2011

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In water, on water, and by water: mimicking nature's aldolases with organocatalysis and water

Organic & biomolecular chemistry, 2010-09, Vol.8 (18), p.443-45

2010

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Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies

ACS catalysis, 2014-03, Vol.4 (3), p.743-762

2014

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Targeted gene knockout by direct delivery of zinc-finger nuclease proteins

Nature methods, 2012-08, Vol.9 (8), p.805

2012

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Thiourea-Catalyzed Highly Enantio- and Diastereoselective Additions of Oxindoles to Nitroolefins: Application to the Formal Synthesis of (+)-Physostigmine

Journal of the American Chemical Society, 2009-07, Vol.131 (25), p.8758-8759

2009

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Synthetic Zinc Finger Proteins: The Advent of Targeted Gene Regulation and Genome Modification Technologies

Accounts of chemical research, 2014-08, Vol.47 (8), p.2309-2318

2014

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De Novo Computational Design of Retro-Aldol Enzymes

Science (American Association for the Advancement of Science), 2008-03, Vol.319 (5868), p.1387-1391

2008

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Efficient delivery of nuclease proteins for genome editing in human stem cells and primary cells

Nature protocols, 2015-11, Vol.10 (11), p.1842-1859

2015

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Site-Selective Labeling of a Lysine Residue in Human Serum Albumin

Angewandte Chemie (International ed.), 2014-10, Vol.53 (44), p.11783-11786

International ed. in English, 2014

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Tyrosine Bioconjugation through Aqueous Ene-Type Reactions: A Click-Like Reaction for Tyrosine

Journal of the American Chemical Society, 2010-02, Vol.132 (5), p.1523-1525

2010

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anti-Selective Asymmetric Michael Reactions of Aldehydes and Nitroolefins Catalyzed by a Primary Amine/Thiourea

Angewandte Chemie (International ed.), 2009-12, Vol.48 (52), p.9848-9852

2009

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Highly Efficient Hydrogen-Bonding Catalysis of the Diels–Alder Reaction of 3-Vinylindoles and Methyleneindolinones Provides Carbazolespirooxindole Skeletons

Journal of the American Chemical Society, 2011-08, Vol.133 (32), p.12354-12357

2011

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Assembly of Spirooxindole Derivatives Containing Four Consecutive Stereocenters via Organocatalytic Michael–Henry Cascade Reactions

Organic letters, 2012-04, Vol.14 (7), p.1834-1837

2012

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Directed Evolution of an Enhanced and Highly Efficient FokI Cleavage Domain for Zinc Finger Nucleases

Journal of molecular biology, 2010-07, Vol.400 (1), p.96-107

2010

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Core Structure-Based Design of Organocatalytic [3+2]-Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles

Chemistry : a European journal, 2012-01, Vol.18 (1), p.63-67

2012

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Dimeric Quinidine-Catalyzed Enantioselective Aminooxygenation of Oxindoles: An Organocatalytic Approach to 3-Hydroxyoxindole Derivatives

Journal of the American Chemical Society, 2010-04, Vol.132 (16), p.5574-5575

2010

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Selective arylthiolane deprotection by singlet oxygen: a promising tool for sensors and prodrugs

Chemical communications (Cambridge, England), 2015-02, Vol.51 (15), p.3196-3199

2015

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Directed evolution of the TALE N-terminal domain for recognition of all 5' bases

Nucleic acids research, 2013-11, Vol.41 (21), p.9779

2013

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A Way to Highly Enantiomerically Enriched aza-Morita-Baylis-Hillman-Type Products

Angewandte Chemie (International ed.), 2007-01, Vol.46 (11), p.1878-1880

2007

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The ErbB2/ErbB3 Heterodimer Functions as an Oncogenic Unit: ErbB2 Requires ErbB3 to Drive Breast Tumor Cell Proliferation

Proceedings of the National Academy of Sciences - PNAS, 2003-07, Vol.100 (15), p.8933-8938

2003

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Organocatalysis Lost: Modern Chemistry, Ancient Chemistry, and an Unseen Biosynthetic Apparatus

Cell-penetrating peptide-mediated delivery of TALEN proteins via bioconjugation for genome engineering

Rapid, Stable, Chemoselective Labeling of Thiols with Julia-Kocieński-like Reagents: A Serum-Stable Alternative to Maleimide-Based Protein Conjugation

Organocatalytic Amidation and Esterification of Aldehydes with Activating Reagents by a Cross-Coupling Strategy

Core-Structure-Motivated Design of a Phosphine-Catalyzed [3 + 2] Cycloaddition Reaction: Enantioselective Syntheses of Spirocyclopenteneoxindoles

Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst

In water, on water, and by water: mimicking nature's aldolases with organocatalysis and water

Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies

Targeted gene knockout by direct delivery of zinc-finger nuclease proteins

Thiourea-Catalyzed Highly Enantio- and Diastereoselective Additions of Oxindoles to Nitroolefins: Application to the Formal Synthesis of (+)-Physostigmine

Synthetic Zinc Finger Proteins: The Advent of Targeted Gene Regulation and Genome Modification Technologies

De Novo Computational Design of Retro-Aldol Enzymes

Efficient delivery of nuclease proteins for genome editing in human stem cells and primary cells

Site-Selective Labeling of a Lysine Residue in Human Serum Albumin

Tyrosine Bioconjugation through Aqueous Ene-Type Reactions: A Click-Like Reaction for Tyrosine

anti-Selective Asymmetric Michael Reactions of Aldehydes and Nitroolefins Catalyzed by a Primary Amine/Thiourea

Highly Efficient Hydrogen-Bonding Catalysis of the Diels–Alder Reaction of 3-Vinylindoles and Methyleneindolinones Provides Carbazolespirooxindole Skeletons

Assembly of Spirooxindole Derivatives Containing Four Consecutive Stereocenters via Organocatalytic Michael–Henry Cascade Reactions

Directed Evolution of an Enhanced and Highly Efficient FokI Cleavage Domain for Zinc Finger Nucleases

Core Structure-Based Design of Organocatalytic [3+2]-Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles

Dimeric Quinidine-Catalyzed Enantioselective Aminooxygenation of Oxindoles: An Organocatalytic Approach to 3-Hydroxyoxindole Derivatives

Selective arylthiolane deprotection by singlet oxygen: a promising tool for sensors and prodrugs

Directed evolution of the TALE N-terminal domain for recognition of all 5' bases

A Way to Highly Enantiomerically Enriched aza-Morita-Baylis-Hillman-Type Products

The ErbB2/ErbB3 Heterodimer Functions as an Oncogenic Unit: ErbB2 Requires ErbB3 to Drive Breast Tumor Cell Proliferation

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