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Total Synthesis of (±)- and (+)-Valienamine via a Strategy Derived from New Palladium-Catalyzed Reactions

Journal of the American Chemical Society, 1998-03, Vol.120 (8), p.1732-1740

1998

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Palladium-Catalyzed Cross-Coupling Reactions of Benzyl Indium Reagents with Aryl Iodides

Journal of organic chemistry, 2009-02, Vol.74 (3), p.1388-1390

2009

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Structure activity relationship studies on chemically non-reactive glycine sulfonamide inhibitors of diacylglycerol lipase

Bioorganic & medicinal chemistry, 2016-04, Vol.24 (7), p.1455-1468

2016

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Screening and characterization of reactive compounds with in vitro peptide-trapping and liquid chromatography/high-resolution accurate mass spectrometry

Journal of biomolecular screening, 2014-02, Vol.19 (2), p.297-307

2014

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Short Preparation of (S)-(E)-1-(O-Methylmandeloxy)butadiene

Journal of organic chemistry, 1997-02, Vol.62 (3), p.736-736

1997

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Isoxazolyl, oxazolyl, and thiazolylpropionic acid derivatives as potent α4β1 integrin antagonists

Bioorganic & medicinal chemistry letters, 2001-10, Vol.11 (19), p.2593-2596

2001

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ChemInform Abstract: Pauson-Khand Reaction

ChemInform, 2011-05, Vol.42 (18), p.no-no

Chupak, Louis S.

2011

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Isoxazolyl, oxazolyl, and thiazolylpropionic acid derivatives as potent α 4β 1 integrin antagonists

Bioorganic & medicinal chemistry letters, 2001, Vol.11 (19), p.2593-2596

2001

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ChemInform Abstract: Palladium-Catalyzed Cross-Coupling Reactions of Benzyl Indium Reagents with Aryl Iodides

ChemInform, 2009-06, Vol.40 (25), p.no-no

2009

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DGKα/ζ inhibitors combine with PD-1 checkpoint therapy to promote T cell-mediated antitumor immunity

Science translational medicine, 2023-10, Vol.15 (719), p.eadh1892

2023

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Discovery of Potent, Dual-Inhibitors of Diacylglycerol Kinases Alpha and Zeta Guided by Phenotypic Optimization

ACS medicinal chemistry letters, 2023-07, Vol.14 (7), p.929-935

2023

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Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymerase

Bioorganic & medicinal chemistry letters, 2011-04, Vol.21 (8), p.2212-2215

2011

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SAR studies on a series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides: Potent inhibitors of the polymerase enzyme (NS5B) of the hepatitis C virus

Bioorganic & medicinal chemistry letters, 2011-05, Vol.21 (10), p.3142-3147

2011

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Corrigendum to “Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymerase” [Bioorg. Med. Chem. Lett. 21 (2011) 2212]

Bioorganic & medicinal chemistry letters, 2011-09, Vol.21 (18), p.5650-5651

2011

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ChemInform Abstract: Doetz Benzannulation

ChemInform, 2011-08, Vol.42 (31), p.no-no

Chupak, Louis

2011

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Stereocontrolled palladium(0) catalyzed allylic alkylations in the total synthesis of (+)-valienamine and studies toward the application of transition metal catalyzed metathesis reactions for the synthesis of taxanes

Chupak, Louis Stanley

1998

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Total Synthesis of (±)- and (+)-Valienamine via a Strategy Derived from New Palladium-Catalyzed Reactions

Palladium-Catalyzed Cross-Coupling Reactions of Benzyl Indium Reagents with Aryl Iodides

Structure activity relationship studies on chemically non-reactive glycine sulfonamide inhibitors of diacylglycerol lipase

Screening and characterization of reactive compounds with in vitro peptide-trapping and liquid chromatography/high-resolution accurate mass spectrometry

Short Preparation of (S)-(E)-1-(O-Methylmandeloxy)butadiene

Isoxazolyl, oxazolyl, and thiazolylpropionic acid derivatives as potent α4β1 integrin antagonists

ChemInform Abstract: Pauson-Khand Reaction

Isoxazolyl, oxazolyl, and thiazolylpropionic acid derivatives as potent α 4β 1 integrin antagonists

ChemInform Abstract: Palladium-Catalyzed Cross-Coupling Reactions of Benzyl Indium Reagents with Aryl Iodides

DGKα/ζ inhibitors combine with PD-1 checkpoint therapy to promote T cell-mediated antitumor immunity

Discovery of Potent, Dual-Inhibitors of Diacylglycerol Kinases Alpha and Zeta Guided by Phenotypic Optimization

Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymerase

SAR studies on a series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides: Potent inhibitors of the polymerase enzyme (NS5B) of the hepatitis C virus

Corrigendum to “Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymerase” [Bioorg. Med. Chem. Lett. 21 (2011) 2212]

ChemInform Abstract: Doetz Benzannulation

Stereocontrolled palladium(0) catalyzed allylic alkylations in the total synthesis of (+)-valienamine and studies toward the application of transition metal catalyzed metathesis reactions for the synthesis of taxanes

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