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Total synthesis of taxol

Nature (London), 1994-02, Vol.367 (6464), p.630-634

1994

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Total Synthesis of Taxol. 4. The Final Stages and Completion of the Synthesis

Journal of the American Chemical Society, 1995, Vol.117 (2), p.653-659

1995

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Total Synthesis of Taxol. 1. Retrosynthesis, Degradation, and Reconstitution

Journal of the American Chemical Society, 1995, Vol.117 (2), p.624-633

1995

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Total Synthesis of Taxol. 3. Formation of Taxol's ABC Ring Skeleton

Journal of the American Chemical Society, 1995, Vol.117 (2), p.645-652

1995

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Total Synthesis of taxol. 2. Construction of A and C ring intermediates and initial attempts to construct the ABC ring system

Journal of the American Chemical Society, 1995-01, Vol.117 (2), p.634-644

1995

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In vitro and in vivo evaluation of dihydropyrimidinone C-5 amides as potent and selective alpha(1A) receptor antagonists for the treatment of benign prostatic hyperplasia

Journal of medicinal chemistry, 2000-07, Vol.43 (14), p.2703-2718

2000

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Chemical Synthesis and Biological Evaluation of C-2 Taxoids

Journal of the American Chemical Society, 1995-03, Vol.117 (9), p.2409-2420

1995

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Discovery and initial structure–Activity relationships of trisubstituted ureas as thrombin receptor (PAR-1) antagonists

Bioorganic & medicinal chemistry letters, 2001-10, Vol.11 (20), p.2691-2696

2001

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Synthesis of Novel Taxoids

Journal of the American Chemical Society, 1994-02, Vol.116 (4), p.1591-1592

1994

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Synthesis of C-2 Taxol Analogues

Angewandte Chemie (International ed.), 1994-09, Vol.33 (15-16), p.1581-1583

1994

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Addition of zinc homoenolates to acetylenic esters and amides: a formal [3 + 2] cycloaddition

Journal of organic chemistry, 1993-02, Vol.58 (5), p.1038-1047

1993

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A facile three-step synthesis of 1,2-amino alcohols using the Ellman homochiral tert-butylsulfinamide

Tetrahedron letters, 2001-03, Vol.42 (11), p.2051-2054

2001

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Discovery and Evaluation of Potent P 1 Aryl Heterocycle-Based Thrombin Inhibitors

Journal of medicinal chemistry, 2004-06, Vol.47 (12), p.2995-3008

2004

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The Total Synthesis of (±)-Ginkgolide B

Journal of the American Chemical Society, 2000-09, Vol.122 (35), p.8453-8463

2000

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Novel chemistry of taxol. Retrosynthetic and synthetic studies

Journal of the Chemical Society. Chemical communications, 1994 (3), p.295

1994

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9-Hydroxyazafluorenes and Their Use in Thrombin Inhibitors

Journal of medicinal chemistry, 2005-04, Vol.48 (7), p.2282-2293

2005

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Total synthesis of Taxol. 2. construction of A and C ring intermediates and initial attempts to construct the ABC ring system. [Erratum to document cited in CA122:160984]

Journal of the American Chemical Society, 1995-08, Vol.117 (33), p.8690-8690

1995

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Synthesis and Evaluation of Imidazole Acetic Acid Inhibitors of Activated Thrombin-Activatable Fibrinolysis Inhibitor as Novel Antithrombotics

Journal of medicinal chemistry, 2003-12, Vol.46 (25), p.5294-5297

2003

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Potent thrombin inhibitors via a 20-membered ring olefin metathesis macrocyclization

Tetrahedron letters, 2003-03, Vol.44 (11), p.2401-2404

2003

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Unexpected enhancement of thrombin inhibitor potency with o-aminoalkylbenzylamides in the P1 position

Bioorganic & medicinal chemistry letters, 2003-10, Vol.13 (20), p.3477-3482

2003

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Design and synthesis of potent and selective macrocyclic thrombin inhibitors

Bioorganic & medicinal chemistry letters, 2003-08, Vol.13 (16), p.2781-2784

2003

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Discovery of a nonpeptidic small molecule antagonist of the human platelet thrombin receptor (PAR-1)

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (3), p.319-323

2002

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Total Synthesis of (±)-Ginkgolide B

Journal of the American Chemical Society, 1999-11, Vol.121 (43), p.10249-10250

1999

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Non-peptidic small-molecule antagonists of the human platelet thrombin receptor PAR-1

Current medicinal chemistry. Cardiovascular and hematological agents, 2003-03, Vol.1 (1), p.47

2003

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P 2 pyridine N-oxide thrombin inhibitors: a novel peptidomimetic scaffold

Bioorganic & medicinal chemistry letters, 2005-06, Vol.15 (11), p.2771-2775

2005

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Total synthesis of taxol

Total Synthesis of Taxol. 4. The Final Stages and Completion of the Synthesis

Total Synthesis of Taxol. 1. Retrosynthesis, Degradation, and Reconstitution

Total Synthesis of Taxol. 3. Formation of Taxol's ABC Ring Skeleton

Total Synthesis of taxol. 2. Construction of A and C ring intermediates and initial attempts to construct the ABC ring system

In vitro and in vivo evaluation of dihydropyrimidinone C-5 amides as potent and selective alpha(1A) receptor antagonists for the treatment of benign prostatic hyperplasia

Chemical Synthesis and Biological Evaluation of C-2 Taxoids

Discovery and initial structure–Activity relationships of trisubstituted ureas as thrombin receptor (PAR-1) antagonists

Synthesis of Novel Taxoids

Synthesis of C-2 Taxol Analogues

Addition of zinc homoenolates to acetylenic esters and amides: a formal [3 + 2] cycloaddition

A facile three-step synthesis of 1,2-amino alcohols using the Ellman homochiral tert-butylsulfinamide

Discovery and Evaluation of Potent P 1 Aryl Heterocycle-Based Thrombin Inhibitors

The Total Synthesis of (±)-Ginkgolide B

Novel chemistry of taxol. Retrosynthetic and synthetic studies

9-Hydroxyazafluorenes and Their Use in Thrombin Inhibitors

Total synthesis of Taxol. 2. construction of A and C ring intermediates and initial attempts to construct the ABC ring system. [Erratum to document cited in CA122:160984]

Synthesis and Evaluation of Imidazole Acetic Acid Inhibitors of Activated Thrombin-Activatable Fibrinolysis Inhibitor as Novel Antithrombotics

Potent thrombin inhibitors via a 20-membered ring olefin metathesis macrocyclization

Unexpected enhancement of thrombin inhibitor potency with o-aminoalkylbenzylamides in the P1 position

Design and synthesis of potent and selective macrocyclic thrombin inhibitors

Discovery of a nonpeptidic small molecule antagonist of the human platelet thrombin receptor (PAR-1)

Total Synthesis of (±)-Ginkgolide B

Non-peptidic small-molecule antagonists of the human platelet thrombin receptor PAR-1

P 2 pyridine N-oxide thrombin inhibitors: a novel peptidomimetic scaffold

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