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Peptide Synthesis Catalyzed by an Antibody Containing a Binding Site for Variable Amino Acids

Science (American Association for the Advancement of Science), 1994-07, Vol.265 (5169), p.234-237

1994

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Oleocanthal inhibits proliferation and MIP-1α expression in human multiple myeloma cells

Current medicinal chemistry, 2013-06, Vol.20 (19), p.2467-2475

2013

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Determination of the Absolute Configurations of Natural Products via Density Functional Theory Calculations of Optical Rotation, Electronic Circular Dichroism, and Vibrational Circular Dichroism: The Cytotoxic Sesquiterpene Natural Products Quadrone, Suberosenone, Suberosanone, and Suberosenol A Acetate

Journal of natural products (Washington, D.C.), 2006-07, Vol.69 (7), p.1055-1064

2006

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Total Synthesis of (+)-Phorboxazole A Exploiting the Petasis−Ferrier Rearrangement

Journal of the American Chemical Society, 2001-11, Vol.123 (44), p.10942-10953

2001

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Modulation of protein-protein interactions as a therapeutic strategy for the treatment of neurodegenerative tauopathies

Current topics in medicinal chemistry, 2011-02, Vol.11 (3), p.317-330

2011

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Total Synthesis of (+)-Zampanolide

Journal of the American Chemical Society, 2001-12, Vol.123 (49), p.12426-12427

2001

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Total Synthesis of (−)-Cylindrocyclophanes A and F Exploiting the Reversible Nature of the Olefin Cross Metathesis Reaction

Journal of the American Chemical Society, 2001-06, Vol.123 (25), p.5925-5937

2001

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Total Synthesis of (−)-Callystatin A

Organic letters, 2001-05, Vol.3 (11), p.1685-1688

2001

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Total Synthesis of (+)-Phorboxazole A

Journal of the American Chemical Society, 2001-05, Vol.123 (20), p.4834-4836

2001

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Taxol and Discodermolide Represent a Synergistic Drug Combination in Human Carcinoma Cell Lines

Clinical cancer research, 2000-05, Vol.6 (5), p.1978

2000

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Gram-Scale Synthesis of (+)-Discodermolide

Organic letters, 1999-12, Vol.1 (11), p.1823-1826

1999

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On the Reversible Nature of the Olefin Cross Metathesis Reaction

Journal of the American Chemical Society, 2001-02, Vol.123 (5), p.990-991

2001

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Total Synthesis of the Ansamycin Antibiotic (+)-Thiazinotrienomycin E

Journal of organic chemistry, 2000-06, Vol.65 (12), p.3738-3753

2000

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Solution Structure of (+)-Discodermolide

Organic letters, 2001-03, Vol.3 (5), p.695-698

2001

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Tremorgenic Indole Alkaloids Potently Inhibit Smooth Muscle High-Conductance Calcium-Activated Potassium Channels

Biochemistry (Easton), 1994-05, Vol.33 (19), p.5819-5828

1994

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Development of an Efficient, Regio- and Stereoselective Route to Libraries Based on the β-d-Glucose Scaffold

Journal of organic chemistry, 2000-12, Vol.65 (24), p.8307-8316

2000

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Design and Synthesis of Novel Scaffolds for Drug Discovery: Hybrids of β-d-Glucose with 1,2,3,4-Tetrahydrobenzo[e][1,4]diazepin-5-one, the Corresponding 1-Oxazepine, and 2- and 4-Pyridyldiazepines

Organic letters, 2001-04, Vol.3 (7), p.1089-1092

2001

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Multicomponent Linchpin Couplings of Silyl Dithianes: Synthesis of the Schreiber C(16−28) Trisacetonide Subtarget for Mycoticins A and B

Organic letters, 1999-12, Vol.1 (12), p.2001-2004

1999

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Phorboxazole Synthetic Studies. 1. Construction of a C(3−19) Subtarget Exploiting an Extension of the Petasis−Ferrier Rearrangement

Organic letters, 1999-09, Vol.1 (6), p.909-912

1999

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Synthesis of Tedanolide and 13-Deoxytedanolide. Assembly of a Common C(1)−C(11) Subtarget

Organic letters, 1999-10, Vol.1 (8), p.1249-1252

1999

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Modulation of Receptor and Receptor Subtype Affinities Using Diastereomeric and Enantiomeric Monosaccharide Scaffolds as a Means to Structural and Biological Diversity. A New Route to Ether Synthesis

Journal of medicinal chemistry, 1998-04, Vol.41 (9), p.1382-1391

1998

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Phorboxazole Synthetic Studies. 2. Construction of a C(20−28) Subtarget, a Further Extension of the Petasis−Ferrier Rearrangement

Organic letters, 1999-09, Vol.1 (6), p.913-916

1999

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Nodulisporic Acid A Synthetic Studies. 2. Construction of an Eastern Hemisphere Subtarget

Organic letters, 2001-11, Vol.3 (24), p.3971-3974

2001

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Orientational disorder in solvent-free solid c70

Science (American Association for the Advancement of Science), 1991-11, Vol.254 (5036), p.1350-1353

1991

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First Generation Design, Synthesis, and Evaluation of Azepine-Based Cryptophycin Analogues

Organic letters, 2001-12, Vol.3 (25), p.4063-4066

2001

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Peptide Synthesis Catalyzed by an Antibody Containing a Binding Site for Variable Amino Acids

Oleocanthal inhibits proliferation and MIP-1α expression in human multiple myeloma cells

Total Synthesis of (+)-Phorboxazole A Exploiting the Petasis−Ferrier Rearrangement

Modulation of protein-protein interactions as a therapeutic strategy for the treatment of neurodegenerative tauopathies

Total Synthesis of (+)-Zampanolide

Total Synthesis of (−)-Cylindrocyclophanes A and F Exploiting the Reversible Nature of the Olefin Cross Metathesis Reaction

Total Synthesis of (−)-Callystatin A

Total Synthesis of (+)-Phorboxazole A

Taxol and Discodermolide Represent a Synergistic Drug Combination in Human Carcinoma Cell Lines

Gram-Scale Synthesis of (+)-Discodermolide

On the Reversible Nature of the Olefin Cross Metathesis Reaction

Total Synthesis of the Ansamycin Antibiotic (+)-Thiazinotrienomycin E

Solution Structure of (+)-Discodermolide

Tremorgenic Indole Alkaloids Potently Inhibit Smooth Muscle High-Conductance Calcium-Activated Potassium Channels

Development of an Efficient, Regio- and Stereoselective Route to Libraries Based on the β-d-Glucose Scaffold

Design and Synthesis of Novel Scaffolds for Drug Discovery: Hybrids of β-d-Glucose with 1,2,3,4-Tetrahydrobenzo[e][1,4]diazepin-5-one, the Corresponding 1-Oxazepine, and 2- and 4-Pyridyldiazepines

Multicomponent Linchpin Couplings of Silyl Dithianes: Synthesis of the Schreiber C(16−28) Trisacetonide Subtarget for Mycoticins A and B

Phorboxazole Synthetic Studies. 1. Construction of a C(3−19) Subtarget Exploiting an Extension of the Petasis−Ferrier Rearrangement

Synthesis of Tedanolide and 13-Deoxytedanolide. Assembly of a Common C(1)−C(11) Subtarget

Modulation of Receptor and Receptor Subtype Affinities Using Diastereomeric and Enantiomeric Monosaccharide Scaffolds as a Means to Structural and Biological Diversity. A New Route to Ether Synthesis

Phorboxazole Synthetic Studies. 2. Construction of a C(20−28) Subtarget, a Further Extension of the Petasis−Ferrier Rearrangement

Nodulisporic Acid A Synthetic Studies. 2. Construction of an Eastern Hemisphere Subtarget

Orientational disorder in solvent-free solid c70

First Generation Design, Synthesis, and Evaluation of Azepine-Based Cryptophycin Analogues

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