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Unprecedented Catalytic Three Component One-Pot Condensation Reaction: An Efficient Synthesis of 5-Alkoxycarbonyl- 4-aryl-3,4-dihydropyrimidin-2(1H)-ones

Journal of organic chemistry, 1998-05, Vol.63 (10), p.3454-3457

1998

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Asymmetric reduction of keto oxime ethers using oxazaborolidine reagents. The enantioselective synthesis of cyclic amino alcohols

Tetrahedron letters, 1995-06, Vol.36 (25), p.4337-4340

1995

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Efficient catalytic asymmetric alkylations. 3. A kinetic and mechanistic study of the enantioselective phase-transfer methylation of 6,7-dichloro-5-methoxy-2-phenyl-1-indanone

Journal of organic chemistry, 1987-10, Vol.52 (21), p.4745-4752

1987

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An improved method for chiral oxazaborolidine-catalyzed reduction of 4-chromanone analogs and MK-0499

Tetrahedron letters, 1994-08, Vol.35 (35), p.6409-6412

1994

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A practical preparation of diisopropyl phosphoryl protected amino acids

Tetrahedron letters, 1998-12, Vol.39 (52), p.9583-9586

1998

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A Double Ring Closing Metathesis Reaction in the Rapid, Enantioselective Synthesis of NK-1 Receptor Antagonists

Organic letters, 2001-03, Vol.3 (5), p.671-674

2001

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An expedient one-pot synthesis for protected 2-thia-5-azabicyclo[2.2.1]heptan-3-ones. Versatile intermediates in the synthesis of carbapenem sidechains

Tetrahedron letters, 1996-04, Vol.37 (17), p.2919-2922

1996

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A new synthesis of 1,2,4-triazolin-5-ones: application to the convergent synthesis of an NK1 antagonist

Tetrahedron letters, 2000-10, Vol.41 (44), p.8661-8664

2000

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Efficient Synthesis of α-Chloro Ketones via Reaction of Organometallic Reagents with N-Methoxy-N-Methylchloroacetamide

Synlett, 1996, Vol.1996 (3), p.225-226

1996

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Methoxymethylation of Alcohols, Phenols, and Avermectin Aglycones Using MOM-2-pyridylsulfide

Journal of organic chemistry, 1999-04, Vol.64 (7), p.2446-2449

1999

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Observations on the DDQ Oxidation of 1-Acyldihydropyridines - A Synthetic Application

Synthesis (Stuttgart), 2001, Vol.2001 (12), p.1784-1789

2001

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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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Acylimidazolides as Versatile Synthetic Intermediates for the Preparation of Sterically Congested Amides and Ketones: A Practical Synthesis of Proscar

Synthetic communications, 1990-09, Vol.20 (17), p.2683-2690

1990

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Practical Asymmetric Synthesis of a γ-Secretase Inhibitor Exploiting Substrate-Controlled Intramolecular Nitrile Oxide−Olefin Cycloaddition

Journal of organic chemistry, 2006-04, Vol.71 (8), p.3086-3092

2006

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Practical Synthesis of Aryl Triflates under Aqueous Conditions

Organic letters, 2002-12, Vol.4 (26), p.4717-4718

2002

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Silylation-mediated oxidation of 4-aza-3-ketosteroids with DDQ proceeds via DDQ-substrate adducts

Journal of the American Chemical Society, 1988-05, Vol.110 (10), p.3318-3319

1988

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Synthesis of a NO-Releasing Prodrug of Rofecoxib

Journal of organic chemistry, 2006-01, Vol.71 (2), p.480-491

2006

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Practical and efficient synthesis of N-halo compounds

Tetrahedron letters, 2005-02, Vol.46 (7), p.1099-1101

2005

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Stereoselective Synthesis of a Potent Thrombin Inhibitor by a Novel P2−P3 Lactone Ring Opening

Journal of organic chemistry, 2004-05, Vol.69 (11), p.3620-3627

2004

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A New General Method for Preparation of N-Methoxy-N-methylamides. Application in Direct Conversion of an Ester to a Ketone

Tetrahedron letters, 1995-07, Vol.36 (31), p.5461-5464

Williams, J

1995

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Practical Asymmetric Synthesis of Aprepitant, a Potent Human NK-1 Receptor Antagonist, via a Stereoselective Lewis Acid-Catalyzed Trans Acetalization Reaction

Journal of organic chemistry, 2002-09, Vol.67 (19), p.6743-6747

2002

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Practical Asymmetric Synthesis of an Endothelin Receptor Antagonist

Journal of organic chemistry, 1999-12, Vol.64 (26), p.9658-9667

1999

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Practical Synthesis of the New Carbapenem Antibiotic Ertapenem Sodium

Journal of organic chemistry, 2005-09, Vol.70 (19), p.7479-7487

2005

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Asymmetric Synthesis of MK-0499

Journal of organic chemistry, 1995-07, Vol.60 (14), p.4324-4330

1995

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Stereoselective double ring closing metathesis reactions in the synthesis of spirocyclic compounds

Tetrahedron letters, 2000-03, Vol.41 (12), p.2027-2029

2000

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Unprecedented Catalytic Three Component One-Pot Condensation Reaction: An Efficient Synthesis of 5-Alkoxycarbonyl- 4-aryl-3,4-dihydropyrimidin-2(1H)-ones

Asymmetric reduction of keto oxime ethers using oxazaborolidine reagents. The enantioselective synthesis of cyclic amino alcohols

Efficient catalytic asymmetric alkylations. 3. A kinetic and mechanistic study of the enantioselective phase-transfer methylation of 6,7-dichloro-5-methoxy-2-phenyl-1-indanone

An improved method for chiral oxazaborolidine-catalyzed reduction of 4-chromanone analogs and MK-0499

A practical preparation of diisopropyl phosphoryl protected amino acids

A Double Ring Closing Metathesis Reaction in the Rapid, Enantioselective Synthesis of NK-1 Receptor Antagonists

An expedient one-pot synthesis for protected 2-thia-5-azabicyclo[2.2.1]heptan-3-ones. Versatile intermediates in the synthesis of carbapenem sidechains

A new synthesis of 1,2,4-triazolin-5-ones: application to the convergent synthesis of an NK1 antagonist

Efficient Synthesis of α-Chloro Ketones via Reaction of Organometallic Reagents with N-Methoxy-N-Methylchloroacetamide

Methoxymethylation of Alcohols, Phenols, and Avermectin Aglycones Using MOM-2-pyridylsulfide

Observations on the DDQ Oxidation of 1-Acyldihydropyridines - A Synthetic Application

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

Acylimidazolides as Versatile Synthetic Intermediates for the Preparation of Sterically Congested Amides and Ketones: A Practical Synthesis of Proscar

Practical Asymmetric Synthesis of a γ-Secretase Inhibitor Exploiting Substrate-Controlled Intramolecular Nitrile Oxide−Olefin Cycloaddition

Practical Synthesis of Aryl Triflates under Aqueous Conditions

Silylation-mediated oxidation of 4-aza-3-ketosteroids with DDQ proceeds via DDQ-substrate adducts

Synthesis of a NO-Releasing Prodrug of Rofecoxib

Practical and efficient synthesis of N-halo compounds

Stereoselective Synthesis of a Potent Thrombin Inhibitor by a Novel P2−P3 Lactone Ring Opening

A New General Method for Preparation of N-Methoxy-N-methylamides. Application in Direct Conversion of an Ester to a Ketone

Practical Asymmetric Synthesis of Aprepitant, a Potent Human NK-1 Receptor Antagonist, via a Stereoselective Lewis Acid-Catalyzed Trans Acetalization Reaction

Practical Asymmetric Synthesis of an Endothelin Receptor Antagonist

Practical Synthesis of the New Carbapenem Antibiotic Ertapenem Sodium

Asymmetric Synthesis of MK-0499

Stereoselective double ring closing metathesis reactions in the synthesis of spirocyclic compounds

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