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Synthesis and pharmacology of the enantiomers of cis-7-hydroxy-3-methyl-2-(dipropylamino)tetralin

Journal of medicinal chemistry, 1990-10, Vol.33 (10), p.2925-2929

1990

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Phenyl-substituted analogs of oxotremorine as muscarinic antagonists

Journal of medicinal chemistry, 1992-01, Vol.35 (2), p.285-294

1992

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(S)-5-fluoro-8-hydroxy-2-(dipropylamino)tetralin: a putative 5-HT1A-receptor antagonist

Journal of medicinal chemistry, 1990-06, Vol.33 (6), p.1541-1544

1990

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beta.-Lactam analogs of oxotremorine. 3- and 4-Methyl-substituted 2-azetidinones

Journal of medicinal chemistry, 1990-02, Vol.33 (2), p.580-584

1990

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Novel L-Phe-Gly mimetics

Tetrahedron letters, 1992-07, Vol.33 (31), p.4487-4490

1992

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The formation of 3-methyl-1a,7b-dihydro-1H-cycloprop[ c]isoquinoline from trans-N-[2-(2-acetylphenyl)cyclopropyl]-2-(trimethylsilyl)ethylcarbamate

Tetrahedron letters, 1994-05, Vol.35 (20), p.3417-3420

1994

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Resolved N,N-dialkylated 2-amino-8-hydroxytetralins: stereoselective interactions with 5-HT1A receptors in the brain

Journal of medicinal chemistry, 1989-04, Vol.32 (4), p.779-783

1989

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Stereoselectivity and generality of the palladium-catalysed cyclopropanation of α,β-unsaturated carboxylic acids derivatized with Oppolzer's sultam

J. Chem. Soc., Perkin Trans. 1, 1994 (4), p.461-470

1994

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Urea and 2-imidazolidone derivatives of the muscarinic agents oxotremorine and N-methyl-N-(1-methyl-4-pyrrolidino-2-butynyl)acetamide

Journal of medicinal chemistry, 1992-08, Vol.35 (17), p.3270-3279

1992

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Stereoselective synthesis of methoxy substituted 1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinolines

Tetrahedron, 1987, Vol.43 (22), p.5443-5450

1987

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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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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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Topography and conformational preferences of 6,7,8,9-tetrahydro-1-hydroxy-N,N-dipropyl-5H-benzocyclohepten-6-ylamine. A rationale for the dopaminergic inactivity

Journal of medicinal chemistry, 1989-04, Vol.32 (4), p.765-774

1989

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Conformationally restricted analogs of the muscarinic agent N-methyl-N-(1-methyl-4-pyrrolidino-2-butynyl)acetamide

Journal of medicinal chemistry, 1989-04, Vol.32 (4), p.863-869

1989

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Resolved 3-(3-Hydroxyphenyl)-N-n-propylpiperidine and its analogs: central dopamine receptor activity

Journal of medicinal chemistry, 1984-08, Vol.27 (8), p.1030-1036

1984

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(+)-cis-8-Hydroxy-1-methyl-2-(di-n-propylamino)tetralin: a potent and highly stereoselective 5-hydroxytryptamine receptor agonist

Journal of medicinal chemistry, 1987-11, Vol.30 (11), p.2105-2109

1987

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Resolved pyrrolidine, piperidine, and perhydroazepine analogs of the muscarinic agent N-methyl-N-(1-methyl-4-pyrrolidino-2-butynyl)acetamide

Journal of medicinal chemistry, 1990-12, Vol.33 (12), p.3182-3189

1990

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Derivatives of the muscarinic agent N-methyl-N-(1-methyl-4-pyrrolidino-2-butynyl)acetamide

Journal of medicinal chemistry, 1988-03, Vol.31 (3), p.577-582

1988

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Novel dopamine receptor agonists and antagonists with preferential action on autoreceptors

Journal of medicinal chemistry, 1985-08, Vol.28 (8), p.1049-1053

1985

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N,N-Dialkylated monophenolic trans-2-phenylcyclopropylamines: novel central 5-hydroxytryptamine-receptor agonists

Journal of medicinal chemistry, 1988-01, Vol.31 (1), p.92-99

1988

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Tricarbonylchromium complexes of 2-aminotetralin derivatives. Hydride displacement of aromatic methoxy groups

J. Chem. Soc., Perkin Trans. 1, 1991 (6), p.1453-1459

1991

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C1- and C3-methyl-substituted derivatives of 7-hydroxy-2-(di-n-propylamino)tetralin: activities at central dopamine receptors

Journal of medicinal chemistry, 1987-10, Vol.30 (10), p.1827-1837

1987

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C3-Methylated 5-hydroxy-2-(dipropylamino)tetralins: conformational and steric parameters of importance for central dopamine receptor activation

Journal of medicinal chemistry, 1987-07, Vol.30 (7), p.1135-1144

1987

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(R)- and (S)-5,6,7,8-Tetrahydro-1-hydroxy-N,N-dipropyl-9H-benzocyclohepten-8-ylamine. Stereoselective interactions with 5-HT1A-receptors in the brain

Journal of medicinal chemistry, 1989-10, Vol.32 (10), p.2311-2318

1989

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Improved Preparation, Chromatographic Separation and X-Ray Crystallographic Determination of the Absolute Configuration of the Enantiomers of 8-Hydroxy-2-(dipropylamino)tetralin (8-OH DPAT)

Acta chemica Scandinavica (Copenhagen. 1989), 1988-04, Vol.42b, p.231-236

1988

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Synthesis and pharmacology of the enantiomers of cis-7-hydroxy-3-methyl-2-(dipropylamino)tetralin

Phenyl-substituted analogs of oxotremorine as muscarinic antagonists

(S)-5-fluoro-8-hydroxy-2-(dipropylamino)tetralin: a putative 5-HT1A-receptor antagonist

beta.-Lactam analogs of oxotremorine. 3- and 4-Methyl-substituted 2-azetidinones

Novel L-Phe-Gly mimetics

The formation of 3-methyl-1a,7b-dihydro-1H-cycloprop[ c]isoquinoline from trans-N-[2-(2-acetylphenyl)cyclopropyl]-2-(trimethylsilyl)ethylcarbamate

Resolved N,N-dialkylated 2-amino-8-hydroxytetralins: stereoselective interactions with 5-HT1A receptors in the brain

Stereoselectivity and generality of the palladium-catalysed cyclopropanation of α,β-unsaturated carboxylic acids derivatized with Oppolzer's sultam

Urea and 2-imidazolidone derivatives of the muscarinic agents oxotremorine and N-methyl-N-(1-methyl-4-pyrrolidino-2-butynyl)acetamide

Stereoselective synthesis of methoxy substituted 1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinolines

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

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

Topography and conformational preferences of 6,7,8,9-tetrahydro-1-hydroxy-N,N-dipropyl-5H-benzocyclohepten-6-ylamine. A rationale for the dopaminergic inactivity

Conformationally restricted analogs of the muscarinic agent N-methyl-N-(1-methyl-4-pyrrolidino-2-butynyl)acetamide

Resolved 3-(3-Hydroxyphenyl)-N-n-propylpiperidine and its analogs: central dopamine receptor activity

(+)-cis-8-Hydroxy-1-methyl-2-(di-n-propylamino)tetralin: a potent and highly stereoselective 5-hydroxytryptamine receptor agonist

Resolved pyrrolidine, piperidine, and perhydroazepine analogs of the muscarinic agent N-methyl-N-(1-methyl-4-pyrrolidino-2-butynyl)acetamide

Derivatives of the muscarinic agent N-methyl-N-(1-methyl-4-pyrrolidino-2-butynyl)acetamide

Novel dopamine receptor agonists and antagonists with preferential action on autoreceptors

N,N-Dialkylated monophenolic trans-2-phenylcyclopropylamines: novel central 5-hydroxytryptamine-receptor agonists

Tricarbonylchromium complexes of 2-aminotetralin derivatives. Hydride displacement of aromatic methoxy groups

C1- and C3-methyl-substituted derivatives of 7-hydroxy-2-(di-n-propylamino)tetralin: activities at central dopamine receptors

C3-Methylated 5-hydroxy-2-(dipropylamino)tetralins: conformational and steric parameters of importance for central dopamine receptor activation

(R)- and (S)-5,6,7,8-Tetrahydro-1-hydroxy-N,N-dipropyl-9H-benzocyclohepten-8-ylamine. Stereoselective interactions with 5-HT1A-receptors in the brain

Improved Preparation, Chromatographic Separation and X-Ray Crystallographic Determination of the Absolute Configuration of the Enantiomers of 8-Hydroxy-2-(dipropylamino)tetralin (8-OH DPAT)

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