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1 H and 13 C NMR Spectroscopy of Stereoisomeric 2′-deoxy- C -Nucleosides

Journal of carbohydrate chemistry, 1986-06, Vol.5 (2), p.287-297

1986

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1 The Chemistry and Biochemistry of C-Nucleosides and C-Arylglycosides

Progress in Medicinal Chemistry, 1985, Vol.22, p.1-65

1985

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1H and 13C NMR Spectroscopy of Stereoisomeric 2′-deoxy-C-Nucleosides

Journal of carbohydrate chemistry, 1986-06, Vol.5 (2), p.287-297

1986

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3-(2-Benzofuranyl)quinuclidin-2-ene Derivatives: Novel Muscarinic Antagonists

Journal of medicinal chemistry, 1996-08, Vol.39 (17), p.3269-3277

1996

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A 3-D model for 5-HT1A-receptor agonists based on stereoselective methyl-substituted and conformationally restricted analogues of 8-hydroxy-2-(dipropylamino)tetralin

Journal of medicinal chemistry, 1991-02, Vol.34 (2), p.497-510

1991

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A 3 dimensional model for 5-HT1A-receptor agonists based on stereoselective methyl-substituted and conformationally restricted analogs of 8-hydroxy-2-(dipropylamino)tetralin

Journal of medicinal chemistry, 1991-02, Vol.34 (2), p.497-510

1991

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3-Heteroaryl-Substituted Quinuclidin-3-ol and Quinuclidin-2-ene Derivatives as Muscarinic Antagonists. Synthesis and Structure-Activity Relationships

Journal of medicinal chemistry, 1995-02, Vol.38 (3), p.473-487

1995

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3-Lithioquinuclidin-2-ene: A novel intermediate for the synthesis of muscarinic agonists and antagonists

Bioorganic & medicinal chemistry letters, 1994-12, Vol.4 (24), p.2837-2840

1994

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3-Phenylpiperidines. Central dopamine-autoreceptor stimulating activity

Journal of medicinal chemistry, 1981-12, Vol.24 (12), p.1475-1482

1981

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The 5-HT1A receptor antagonist (S)-UH-301 augments the increase in extracellular concentrations of 5-HT in the frontal cortex produced by both acute and chronic treatment with citalopram

Naunyn-Schmiedeberg's archives of pharmacology, 1996-05, Vol.353 (6), p.630-640

1996

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5-HT1A receptor antagonists increase the activity of serotonergic cells in the dorsal raphe nucleus in rats treated acutely or chronically with citalopram

Naunyn-Schmiedeberg's archives of pharmacology, 1995-08, Vol.352 (2), p.157-165

1995

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The 5-HT1A receptor selective ligands, (R)-8-OH-DPAT and (S)-UH-301, differentially affect the activity of midbrain dopamine neurons

Naunyn-Schmiedeberg's archives of pharmacology, 1993-04, Vol.347 (4), p.353-362

1993

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5 - Modelling of Drug-Receptor Interactions: Stereoselectivity of 5-Hydroxytryptamine and Dopamine Receptors in the Brain

Chirality in Drug Design and Synthesis, 1990, p.83,p1,85-84,p4,100

1990

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5-Oxygenated N-Alkyl-and N,N-Dialkyl-2-amino-1-methyltetralins. Effects of Structure and Stereochemistry on Dopamine-D2-receptor Affinity

Journal of pharmacy and pharmacology, 1991-07, Vol.43 (7), p.481-485

1991

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8-Hydroxy-2-(alkylamino)tetralins and related compounds as central 5-hydroxytryptamine receptor agonists

Journal of medicinal chemistry, 1984-01, Vol.27 (1), p.45-51

1984

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8-Hydroxy-2-(dipropylamino)tetralin, a new centrally acting 5-hydroxytryptamine receptor agonist

Journal of medicinal chemistry, 1981-08, Vol.24 (8), p.921-923

1981

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ACP-103, a 5-hydroxytryptamine 2A receptor inverse agonist, improves the antipsychotic efficacy and side-effect profile of haloperidol and risperidone in experimental models

The Journal of pharmacology and experimental therapeutics, 2007-08, Vol.322 (2), p.862-870

2007

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Amide, urea, and carbamate analogs of the muscarinic agent [4-[[N-(3-chlorophenyl)carbamoyl]oxy]-2-butynyl]trimethylammonium chloride

Journal of medicinal chemistry, 1992-07, Vol.35 (15), p.2787-2798

1992

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Analogs of the Muscarinic Agent 2'‑Methylspiro(1‑azabicyclo[2.2.2]octane)‑3,4'‑[1,3]dioxolane (AF30): Synthesis and Pharmacology

Journal of medicinal chemistry, 1992, Vol.35 (9), p.1541

1992

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Analogs of the muscarinic agent 2'-methylspiro[1-azabicyclo[2.2.2]octane-3,4'-[1,3]dioxolane]: synthesis and pharmacology

Journal of medicinal chemistry, 1992-05, Vol.35 (9), p.1541-1550

1992

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Animal Carotenoids. 32. Carotenoids of Mytilus edulis (Edible Mussel)

Acta chemica Scandinavica (Copenhagen. 1989), 1988, Vol.42b, p.495-503

1988

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Antimuscarinic 3-(2-Furanyl)quinuclidin-2-ene Derivatives: Synthesis and Structure−Activity Relationships

Journal of medicinal chemistry, 1997-11, Vol.40 (23), p.3804-3819

1997

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Apparent syn elimination of palladium oxide from a .beta.-hydroxy organopalladium intermediate

Organometallics, 1983-06, Vol.2 (6), p.772-775

1983

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Atropisomeric Derivatives of 2‘,6‘-Disubstituted ( R )-11-Phenylaporphine: Selective Serotonin 5-HT 7 Receptor Antagonists

Journal of medicinal chemistry, 2001-04, Vol.44 (9), p.1337-1340

2001

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Atropisomeric Derivatives of 2‘,6‘-Disubstituted (R)-11-Phenylaporphine: Selective Serotonin 5-HT7 Receptor Antagonists

Journal of medicinal chemistry, 2001-04, Vol.44 (9), p.1337-1340

2001

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1 H and 13 C NMR Spectroscopy of Stereoisomeric 2′-deoxy- C -Nucleosides

1 The Chemistry and Biochemistry of C-Nucleosides and C-Arylglycosides

1H and 13C NMR Spectroscopy of Stereoisomeric 2′-deoxy-C-Nucleosides

3-(2-Benzofuranyl)quinuclidin-2-ene Derivatives: Novel Muscarinic Antagonists

A 3-D model for 5-HT1A-receptor agonists based on stereoselective methyl-substituted and conformationally restricted analogues of 8-hydroxy-2-(dipropylamino)tetralin

A 3 dimensional model for 5-HT1A-receptor agonists based on stereoselective methyl-substituted and conformationally restricted analogs of 8-hydroxy-2-(dipropylamino)tetralin

3-Heteroaryl-Substituted Quinuclidin-3-ol and Quinuclidin-2-ene Derivatives as Muscarinic Antagonists. Synthesis and Structure-Activity Relationships

3-Lithioquinuclidin-2-ene: A novel intermediate for the synthesis of muscarinic agonists and antagonists

3-Phenylpiperidines. Central dopamine-autoreceptor stimulating activity

The 5-HT1A receptor antagonist (S)-UH-301 augments the increase in extracellular concentrations of 5-HT in the frontal cortex produced by both acute and chronic treatment with citalopram

5-HT1A receptor antagonists increase the activity of serotonergic cells in the dorsal raphe nucleus in rats treated acutely or chronically with citalopram

The 5-HT1A receptor selective ligands, (R)-8-OH-DPAT and (S)-UH-301, differentially affect the activity of midbrain dopamine neurons

5 - Modelling of Drug-Receptor Interactions: Stereoselectivity of 5-Hydroxytryptamine and Dopamine Receptors in the Brain

5-Oxygenated N-Alkyl-and N,N-Dialkyl-2-amino-1-methyltetralins. Effects of Structure and Stereochemistry on Dopamine-D2-receptor Affinity

8-Hydroxy-2-(alkylamino)tetralins and related compounds as central 5-hydroxytryptamine receptor agonists

8-Hydroxy-2-(dipropylamino)tetralin, a new centrally acting 5-hydroxytryptamine receptor agonist

ACP-103, a 5-hydroxytryptamine 2A receptor inverse agonist, improves the antipsychotic efficacy and side-effect profile of haloperidol and risperidone in experimental models

Amide, urea, and carbamate analogs of the muscarinic agent [4-[[N-(3-chlorophenyl)carbamoyl]oxy]-2-butynyl]trimethylammonium chloride

Analogs of the Muscarinic Agent 2'‑Methylspiro(1‑azabicyclo[2.2.2]octane)‑3,4'‑[1,3]dioxolane (AF30): Synthesis and Pharmacology

Analogs of the muscarinic agent 2'-methylspiro[1-azabicyclo[2.2.2]octane-3,4'-[1,3]dioxolane]: synthesis and pharmacology

Animal Carotenoids. 32. Carotenoids of Mytilus edulis (Edible Mussel)

Antimuscarinic 3-(2-Furanyl)quinuclidin-2-ene Derivatives: Synthesis and Structure−Activity Relationships

Apparent syn elimination of palladium oxide from a .beta.-hydroxy organopalladium intermediate

Atropisomeric Derivatives of 2‘,6‘-Disubstituted ( R )-11-Phenylaporphine: Selective Serotonin 5-HT 7 Receptor Antagonists

Atropisomeric Derivatives of 2‘,6‘-Disubstituted (R)-11-Phenylaporphine: Selective Serotonin 5-HT7 Receptor Antagonists

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