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A mechanistic study of the Mitsunobu esterification reaction

Journal of the American Chemical Society, 1988-09, Vol.110 (19), p.6487-6491

1988

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Asymmetric Synthesis of CDP840 by Jacobsen Epoxidation. An Unusual Syn Selective Reduction of an Epoxide

Journal of organic chemistry, 1997-12, Vol.62 (26), p.9223-9228

1997

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A New Planar Chiral Bisphosphine Ligand for Asymmetric Catalysis: Highly Enantioselective Hydrogenations under Mild Conditions

Journal of the American Chemical Society, 1997-07, Vol.119 (26), p.6207-6208

1997

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Total synthesis of immunosuppressant (-)-FK-506

Journal of the American Chemical Society, 1989-02, Vol.111 (3), p.1157-1159

1989

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Highly diastereoselective alkylations of chiral amide enolates: new routes to hydroxyethylene dipeptide isostere inhibitors of HIV-1 protease

Journal of organic chemistry, 1992-05, Vol.57 (10), p.2771-2773

1992

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Highly Enantioselective 1,2-Addition of Lithium Acetylide-Ephedrate Complexes: Spectroscopic Evidence for Reaction Proceeding via a 2:2 Tetramer, and X-ray Characterization of Related Complexes

Journal of the American Chemical Society, 2000-11, Vol.122 (45), p.11212-11218

2000

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Phosphorylated Morpholine Acetal Human Neurokinin-1 Receptor Antagonists as Water-Soluble Prodrugs

Journal of medicinal chemistry, 2000-03, Vol.43 (6), p.1234-1241

2000

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Synthesis of the 5-HT1D receptor agonist MK-0462 via a Pd-catalyzed coupling reaction

Tetrahedron letters, 1994-09, Vol.35 (38), p.6981-6984

1994

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New insights into the mechanism of molybdenum-catalyzed asymmetric alkylation

Pure and applied chemistry, 2004-01, Vol.76 (3), p.625-633

2004

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Efficient Enantioselective Synthesis of Sertraline, a Potent Antidepressant, via a Novel Intramolecular Nucleophilic Addition to Imine

Organic letters, 1999-07, Vol.1 (2), p.293-294

1999

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Discovery, total synthesis, HRV 3C-protease inhibitory activity, and structure–activity relationships of 2-methoxystypandrone and its analogues

Bioorganic & medicinal chemistry letters, 2001-12, Vol.11 (24), p.3143-3146

2001

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Synthesis of unsymmetrical dithioacetals: an efficient synthesis of a novel LTD4 antagonist, L-660,711

Journal of organic chemistry, 1989-07, Vol.54 (15), p.3718-3721

1989

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Asymmetric hydrogenation of tetrahydropyrazines: Synthesis of (S)-piperazine-2-tert-butylcarboxamide, an intermediate in the preparation of the HIV protease inhibitor indinavir

Tetrahedron letters, 1995-09, Vol.36 (36), p.6419-6422

1995

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Variculanol: structure and absolute stereochemistry of a novel 5/12/5 tricyclic sesterterpenoid from Aspergillus variecolor

Journal of organic chemistry, 1991-09, Vol.56 (19), p.5618-5622

1991

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Isolation and identification of impurities in L-696, 229 drug substance

Talanta (Oxford), 1993-07, Vol.40 (7), p.989-994

1993

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A Highly Efficient Synthesis of Fibrinogen Receptor Antagonist L-734,217 via a Novel Chemoselective Silyl-Mediated Conjugate Addition of δ-Lactams to 4-Vinylpyridine

Journal of organic chemistry, 1996-01, Vol.61 (1), p.215-222

1996

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A practical enantioselective synthesis of .alpha.,.alpha.-diaryl-2-pyrrolidinemethanol. Preparation and chemistry of the corresponding oxazaborolidines

Journal of organic chemistry, 1991-01, Vol.56 (2), p.751-762

1991

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ORIGIN OF MONACOLIN L FROM ASPERGILLUS TERREUS CULTURES

The Journal of Antibiotics, 1989/01/25, Vol.42(1), pp.30-36

1989

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Chemistry of FK-506: Benzilic acid rearrangement of the tricarbonyl system

Tetrahedron letters, 1989, Vol.30 (6), p.671-674

1989

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A mechanistic study of the FK-506 tricarbonyl system rearrangement: Synthesis of C.9 Labeled FK-506

Tetrahedron letters, 1989, Vol.30 (45), p.6121-6124

1989

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Efficient degradation of FK-506 to a versatile synthetic intermediate

Journal of organic chemistry, 1990-09, Vol.55 (20), p.5451-5454

1990

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A diastereospecific, non-racemic synthesis of the C.10–C.18 segment of FK-506

Tetrahedron letters, 1988, Vol.29 (3), p.277-280

1988

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Synthesis of the novel sarcosine and proline (FK-525) analogs of FK-506: rearrangement of the allylic ester system

Journal of organic chemistry, 1990-09, Vol.55 (20), p.5448-5450

1990

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Mild Aryl Ether Formation in the Semisynthesis of the Novel Macrolide Immunosuppressant L-732,531

Journal of organic chemistry, 1998-09, Vol.63 (19), p.6721-6726

1998

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An asymmetric synthesis of MK-0417. Observations on oxazaborolidine-catalyzed reductions

Journal of organic chemistry, 1991-01, Vol.56 (2), p.763-769

1991

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A mechanistic study of the Mitsunobu esterification reaction

Asymmetric Synthesis of CDP840 by Jacobsen Epoxidation. An Unusual Syn Selective Reduction of an Epoxide

A New Planar Chiral Bisphosphine Ligand for Asymmetric Catalysis: Highly Enantioselective Hydrogenations under Mild Conditions

Total synthesis of immunosuppressant (-)-FK-506

Highly diastereoselective alkylations of chiral amide enolates: new routes to hydroxyethylene dipeptide isostere inhibitors of HIV-1 protease

Highly Enantioselective 1,2-Addition of Lithium Acetylide-Ephedrate Complexes: Spectroscopic Evidence for Reaction Proceeding via a 2:2 Tetramer, and X-ray Characterization of Related Complexes

Phosphorylated Morpholine Acetal Human Neurokinin-1 Receptor Antagonists as Water-Soluble Prodrugs

Synthesis of the 5-HT1D receptor agonist MK-0462 via a Pd-catalyzed coupling reaction

New insights into the mechanism of molybdenum-catalyzed asymmetric alkylation

Efficient Enantioselective Synthesis of Sertraline, a Potent Antidepressant, via a Novel Intramolecular Nucleophilic Addition to Imine

Discovery, total synthesis, HRV 3C-protease inhibitory activity, and structure–activity relationships of 2-methoxystypandrone and its analogues

Synthesis of unsymmetrical dithioacetals: an efficient synthesis of a novel LTD4 antagonist, L-660,711

Asymmetric hydrogenation of tetrahydropyrazines: Synthesis of (S)-piperazine-2-tert-butylcarboxamide, an intermediate in the preparation of the HIV protease inhibitor indinavir

Variculanol: structure and absolute stereochemistry of a novel 5/12/5 tricyclic sesterterpenoid from Aspergillus variecolor

Isolation and identification of impurities in L-696, 229 drug substance

A Highly Efficient Synthesis of Fibrinogen Receptor Antagonist L-734,217 via a Novel Chemoselective Silyl-Mediated Conjugate Addition of δ-Lactams to 4-Vinylpyridine

A practical enantioselective synthesis of .alpha.,.alpha.-diaryl-2-pyrrolidinemethanol. Preparation and chemistry of the corresponding oxazaborolidines

ORIGIN OF MONACOLIN L FROM ASPERGILLUS TERREUS CULTURES

Chemistry of FK-506: Benzilic acid rearrangement of the tricarbonyl system

A mechanistic study of the FK-506 tricarbonyl system rearrangement: Synthesis of C.9 Labeled FK-506

Efficient degradation of FK-506 to a versatile synthetic intermediate

A diastereospecific, non-racemic synthesis of the C.10–C.18 segment of FK-506

Synthesis of the novel sarcosine and proline (FK-525) analogs of FK-506: rearrangement of the allylic ester system

Mild Aryl Ether Formation in the Semisynthesis of the Novel Macrolide Immunosuppressant L-732,531

An asymmetric synthesis of MK-0417. Observations on oxazaborolidine-catalyzed reductions

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