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Kinase inhibitors as potential therapeutics for acute and chronic neurodegenerative conditions

Current pharmaceutical design, 2009-12, Vol.15 (34), p.3919

Cuny, G D

2009

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Biological Properties of Novel Antistaphylococcal Quinoline-Indole Agents

Antimicrobial Agents and Chemotherapy, 2003-02, Vol.47 (2), p.458-466

2003

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Practical, high-yield, regioselective, rhodium-catalyzed hydroformylation of functionalized .alpha.-olefins

Journal of the American Chemical Society, 1993-03, Vol.115 (5), p.2066-2068

1993

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Photoactivated virucidal properties of tridentate 2,2′-dihydroxyazobenzene and 2-salicylideneaminophenol platinum pyridine complexes

Bioorganic & medicinal chemistry letters, 1999-01, Vol.9 (2), p.237-240

1999

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Chemical inhibitor of nonapoptotic cell death with therapeutic potential for ischemic brain injury

Nature chemical biology, 2005-07, Vol.1 (2), p.112-119

2005

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FDA-preapproved drugs targeted to the translational regulation and processing of the amyloid precursor protein

Journal of molecular neuroscience, 2004-01, Vol.24 (1), p.129-136

2004

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Structure–activity relationship study of novel necroptosis inhibitors

Bioorganic & medicinal chemistry letters, 2005-11, Vol.15 (22), p.5039-5044

2005

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Structure–activity relationship study of novel tissue transglutaminase inhibitors

Bioorganic & medicinal chemistry letters, 2005-04, Vol.15 (7), p.1885-1889

2005

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Synthesis of Hydantoins from Enantiomerically Pure α-Amino Amides without Epimerization

Journal of organic chemistry, 2006-02, Vol.71 (4), p.1750-1753

2006

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Synthesis of (±)-aporphine utilizing Pictet–Spengler and intramolecular phenol ortho-arylation reactions

Tetrahedron letters, 2004-06, Vol.45 (26), p.5167-5170

Cuny, Gregory D.

2004

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Intramolecular ortho-arylation of phenols utilized in the synthesis of the aporphine alkaloids (±)-lirinidine and (±)-nuciferine

Tetrahedron letters, 2003-10, Vol.44 (44), p.8149-8152

Cuny, Gregory D.

2003

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Synthesis of substituted carbazoles and β -carbolines by cyclization of diketoindole derivatives

Tetrahedron letters, 2004-07, Vol.45 (28), p.5411-5413

2004

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Potent In vitro methicillin-resistant Staphylococcus aureus activity of 2-(1 H-indol-3-yl)quinoline derivatives

Bioorganic & medicinal chemistry letters, 2000-12, Vol.10 (23), p.2675-2678

2000

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Ring-opening reactions of cyclic allylic ethers by zirconocene complexes of cyclic alkynes

Organometallics, 1991-01, Vol.10 (1), p.363-365

1991

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Defining Cdk5 Ligand Chemical Space with Small Molecule Inhibitors of Tau Phosphorylation

Chemistry & biology, 2005-07, Vol.12 (7), p.811-823

2005

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Ring opening cross-metathesis on solid support: a combinatorial library synthesis of highly functionalized cyclopentanes

Molecular diversity, 1997, Vol.3 (3), p.173-179

1997

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Cis difunctionalization of cyclic olefins with use of organozirconium intermediates

Organometallics, 1991-03, Vol.10 (3), p.537-539

1991

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Utilization of a copper-catalyzed diaryl ether synthesis for the preparation of verbenachalcone

Tetrahedron, 2002-09, Vol.58 (39), p.7903-7910

2002

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Synthesis, stereochemistry confirmation and biological activity evaluation of a constituent from Isodon excisus

Tetrahedron, 2003-12, Vol.59 (50), p.9961-9969

2003

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Synthesis, receptor binding and functional studies of mesoridazine stereoisomers

Bioorganic & medicinal chemistry letters, 2004-09, Vol.14 (17), p.4379-4382

2004

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Potent In vitro methicillin-resistant Staphylococcus aureus activity of 2-(1 H-indol-3-yl)tetrahydroquinoline derivatives

Bioorganic & medicinal chemistry letters, 2002-01, Vol.12 (2), p.129-132

2002

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Ring opening cross-metathesis on solid support

Tetrahedron letters, 1997-07, Vol.38 (30), p.5237-5240

1997

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Effects of a verbenachalcone derivative on neurite outgrowth, inhibition of caspase induction and gene expression

Bioorganic & medicinal chemistry letters, 2005-02, Vol.15 (4), p.1193-1196

2005

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Rhodium-Catalyzed Hydroformylation of Internal Alkynes to α,β-Unsaturated Aldehydes

Angewandte Chemie (International ed.), 1995-09, Vol.34 (16), p.1760-1761

1995

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Solution-phase ring opening cross-metathesis of bicyclic alkenes with styrene derivatives and its application to “resin capture” solid-phase synthesis

Tetrahedron, 1999-07, Vol.55 (27), p.8169-8178

1999

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Kinase inhibitors as potential therapeutics for acute and chronic neurodegenerative conditions

Biological Properties of Novel Antistaphylococcal Quinoline-Indole Agents

Practical, high-yield, regioselective, rhodium-catalyzed hydroformylation of functionalized .alpha.-olefins

Photoactivated virucidal properties of tridentate 2,2′-dihydroxyazobenzene and 2-salicylideneaminophenol platinum pyridine complexes

Chemical inhibitor of nonapoptotic cell death with therapeutic potential for ischemic brain injury

FDA-preapproved drugs targeted to the translational regulation and processing of the amyloid precursor protein

Structure–activity relationship study of novel necroptosis inhibitors

Structure–activity relationship study of novel tissue transglutaminase inhibitors

Synthesis of Hydantoins from Enantiomerically Pure α-Amino Amides without Epimerization

Synthesis of (±)-aporphine utilizing Pictet–Spengler and intramolecular phenol ortho-arylation reactions

Intramolecular ortho-arylation of phenols utilized in the synthesis of the aporphine alkaloids (±)-lirinidine and (±)-nuciferine

Synthesis of substituted carbazoles and β -carbolines by cyclization of diketoindole derivatives

Potent In vitro methicillin-resistant Staphylococcus aureus activity of 2-(1 H-indol-3-yl)quinoline derivatives

Ring-opening reactions of cyclic allylic ethers by zirconocene complexes of cyclic alkynes

Defining Cdk5 Ligand Chemical Space with Small Molecule Inhibitors of Tau Phosphorylation

Ring opening cross-metathesis on solid support: a combinatorial library synthesis of highly functionalized cyclopentanes

Cis difunctionalization of cyclic olefins with use of organozirconium intermediates

Utilization of a copper-catalyzed diaryl ether synthesis for the preparation of verbenachalcone

Synthesis, stereochemistry confirmation and biological activity evaluation of a constituent from Isodon excisus

Synthesis, receptor binding and functional studies of mesoridazine stereoisomers

Potent In vitro methicillin-resistant Staphylococcus aureus activity of 2-(1 H-indol-3-yl)tetrahydroquinoline derivatives

Ring opening cross-metathesis on solid support

Effects of a verbenachalcone derivative on neurite outgrowth, inhibition of caspase induction and gene expression

Rhodium-Catalyzed Hydroformylation of Internal Alkynes to α,β-Unsaturated Aldehydes

Solution-phase ring opening cross-metathesis of bicyclic alkenes with styrene derivatives and its application to “resin capture” solid-phase synthesis

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