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Highly Regioselective Friedländer Annulations with Unmodified Ketones Employing Novel Amine Catalysts: Syntheses of 2-Substituted Quinolines, 1,8-Naphthyridines, and Related Heterocycles

Journal of organic chemistry, 2003-01, Vol.68 (2), p.467-477

2003

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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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Diastereoselective Reductive Amination of Aryl Trifluoromethyl Ketones and α-Amino Esters

Angewandte Chemie (International ed.), 2007-01, Vol.46 (11), p.1839-1842

2007

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Palladium-Catalyzed Synthesis of Aryl Sulfides from Aryl Triflates

Journal of organic chemistry, 1998-12, Vol.63 (26), p.9606-9607

1998

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Palladium-Catalyzed Regioselective Arylation of Imidazo[1,2-b][1,2,4]triazine: Synthesis of an α2/ 3-Selective GABA Agonist

Journal of organic chemistry, 2005-07, Vol.70 (15), p.5938-5945

2005

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Kinetic Resolution of rac-4,12-Dibromo[2.2]paracyclophane in a Palladium [2.2]PHANEPHOS Catalyzed Amination

Journal of organic chemistry, 1997-09, Vol.62 (19), p.6462-6463

1997

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An Efficient Chemoenzymatic Approach to (S)-γ-Fluoroleucine Ethyl Ester

Journal of organic chemistry, 2005-03, Vol.70 (6), p.2372-2375

2005

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Practical Synthesis of a Potent Hepatitis C Virus RNA Replication Inhibitor

Journal of organic chemistry, 2004-09, Vol.69 (19), p.6257-6266

2004

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Enantioselective Preparation of Ring-Fused 1-Fluorocyclopropane-1-carboxylate Derivatives: En Route to mGluR 2 Receptor Agonist MGS0028

Organic letters, 2004-10, Vol.6 (21), p.3775-3777

2004

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Synthesis of 5-Pyridyl-2-furaldehydes via Palladium-Catalyzed Cross-Coupling with Triorganozincates

Organic letters, 2002-02, Vol.4 (3), p.375-378

2002

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Crystallization-Induced Diastereoselection: Asymmetric Synthesis of Substance P Inhibitors

Chemistry : a European journal, 2002-03, Vol.8 (6), p.1372-1376

2002

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An Efficient Asymmetric Synthesis of an Estrogen Receptor Modulator by Sulfoxide-Directed Borane Reduction

Proceedings of the National Academy of Sciences - PNAS, 2004-04, Vol.101 (16), p.5776-5781

2004

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Practical Synthesis of a Neuropeptide Y Antagonist via Stereoselective Addition to a Ketene

Journal of organic chemistry, 2005-11, Vol.70 (23), p.9222-9229

2005

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A Regioselective Approach to 5-Substituted-3-amino-1,2,4-triazines

Organic letters, 2003-06, Vol.5 (13), p.2271-2274

2003

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Synthesis of a Muscarinic Receptor Antagonist via a Diastereoselective Michael Reaction, Selective Deoxyfluorination and Aromatic Metal−Halogen Exchange Reaction

Journal of organic chemistry, 2001-10, Vol.66 (20), p.6775-6786

2001

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Amination of aryl halides using copper catalysis

Tetrahedron letters, 2001-05, Vol.42 (19), p.3251-3254

2001

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A chemical synthesis of nicotinamide adenine dinucleotide (NAD+)

Chemical communications (Cambridge, England), 1999 (8), p.729-730

1999

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Highly diastereoselective reaction of a chiral, non-racemic amide enolate with ( S)-glycidyl tosylate. Synthesis of the orally active HIV-1 protease inhibitor L-735,524

Tetrahedron letters, 1994, Vol.35 (5), p.673-676

1994

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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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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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Methods for the Synthesis of 5,6,7,8-Tetrahydro-1,8-naphthyridine Fragments for αVβ3 Integrin Antagonists

Journal of organic chemistry, 2004-12, Vol.69 (25), p.8723-8730

2004

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Efficient and Practical Synthesis of a Potent Anti-MRSA β-Methylcarbapenem Containing a Releasable Side Chain

Journal of the American Chemical Society, 1999-12, Vol.121 (49), p.11261-11266

1999

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Tandem Asymmetric Transformations: An Asymmetric 1,2-Migration from a Higher Order Zincate Coupled with a Stereoselective Homoaldol Reaction

Journal of the American Chemical Society, 1996-11, Vol.118 (47), p.11970-11971

1996

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Preparation of (S)-3-Carbethoxy-3-benzylpiperidine and the Growth Hormone Secretagogue L-163,540

Journal of organic chemistry, 1998-12, Vol.63 (25), p.9548-9551

1998

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Highly Regioselective Friedländer Annulations with Unmodified Ketones Employing Novel Amine Catalysts: Syntheses of 2-Substituted Quinolines, 1,8-Naphthyridines, and Related Heterocycles

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

Diastereoselective Reductive Amination of Aryl Trifluoromethyl Ketones and α-Amino Esters

Palladium-Catalyzed Synthesis of Aryl Sulfides from Aryl Triflates

Palladium-Catalyzed Regioselective Arylation of Imidazo[1,2-b][1,2,4]triazine: Synthesis of an α2/ 3-Selective GABA Agonist

Kinetic Resolution of rac-4,12-Dibromo[2.2]paracyclophane in a Palladium [2.2]PHANEPHOS Catalyzed Amination

An Efficient Chemoenzymatic Approach to (S)-γ-Fluoroleucine Ethyl Ester

Practical Synthesis of a Potent Hepatitis C Virus RNA Replication Inhibitor

Enantioselective Preparation of Ring-Fused 1-Fluorocyclopropane-1-carboxylate Derivatives: En Route to mGluR 2 Receptor Agonist MGS0028

Synthesis of 5-Pyridyl-2-furaldehydes via Palladium-Catalyzed Cross-Coupling with Triorganozincates

Crystallization-Induced Diastereoselection: Asymmetric Synthesis of Substance P Inhibitors

An Efficient Asymmetric Synthesis of an Estrogen Receptor Modulator by Sulfoxide-Directed Borane Reduction

Practical Synthesis of a Neuropeptide Y Antagonist via Stereoselective Addition to a Ketene

A Regioselective Approach to 5-Substituted-3-amino-1,2,4-triazines

Synthesis of a Muscarinic Receptor Antagonist via a Diastereoselective Michael Reaction, Selective Deoxyfluorination and Aromatic Metal−Halogen Exchange Reaction

Amination of aryl halides using copper catalysis

A chemical synthesis of nicotinamide adenine dinucleotide (NAD+)

Highly diastereoselective reaction of a chiral, non-racemic amide enolate with ( S)-glycidyl tosylate. Synthesis of the orally active HIV-1 protease inhibitor L-735,524

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

Total synthesis of immunosuppressant (-)-FK-506

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

Methods for the Synthesis of 5,6,7,8-Tetrahydro-1,8-naphthyridine Fragments for αVβ3 Integrin Antagonists

Efficient and Practical Synthesis of a Potent Anti-MRSA β-Methylcarbapenem Containing a Releasable Side Chain

Tandem Asymmetric Transformations: An Asymmetric 1,2-Migration from a Higher Order Zincate Coupled with a Stereoselective Homoaldol Reaction

Preparation of (S)-3-Carbethoxy-3-benzylpiperidine and the Growth Hormone Secretagogue L-163,540

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