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substituted (S)-Phenylpiperidines and Rigid Congeners as Preferential Dopamine Autoreceptor Antagonists: Synthesis and Structure-Activity Relationships

Journal of medicinal chemistry, 1994-08, Vol.37 (17), p.2735-2753

1994

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Dopamine D3 Receptor Antagonists. 1. Synthesis and Structure−Activity Relationships of 5,6-Dimethoxy-N-alkyl- and N-Alkylaryl-Substituted 2-Aminoindans

Journal of medicinal chemistry, 2001-12, Vol.44 (26), p.4716-4732

2001

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C-9 and N-Substituted Analogs of cis-(3aR)-(-)-2,3,3a,4,5,9b-Hexahydro-3-propyl-1H-benz[e]indole-9-carboxamide: 5-HT1A Receptor Agonists with Various Degrees of Metabolic Stability

Journal of medicinal chemistry, 1995-02, Vol.38 (4), p.725-734

1995

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Synthesis and biological activity of C-5 modified derivatives of (+)-AJ76 and (+)-UH232 : increased dopamine D3 receptor preference and improved pharmacokinetic properties

Bioorganic & medicinal chemistry letters, 1994-03, Vol.4 (5), p.689-694

1994

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Synthesis of (r)- and (s)-1-formyl-6,7,8,9-tetrahydro- N,N-(dipropyl)-3H-benz[e]indol-8-amines: Potent and orally active 5-ht1a receptor agonists

Journal of heterocyclic chemistry, 1994-01, Vol.31 (1), p.129-139

1994

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Benzindene prostaglandins. Synthesis of optically pure 15-deoxy-U-68,215 and its enantiomer via a modified intramolecular Wadsworth-Emmons-Wittig reaction

Journal of organic chemistry, 1987-12, Vol.52 (25), p.5594-5601

1987

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(Dipropylamino)-tetrahydronaphthofurans: centrally acting serotonin agonists and dopamine agonists-antagonists

Bioorganic & medicinal chemistry letters, 1997-11, Vol.7 (21), p.2759-2764

1997

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Comparison of 5-HT1A and dopamine D2 pharmacophores. X-ray structures and affinities of conformationally constrained ligands

Journal of medicinal chemistry, 1993-05, Vol.36 (10), p.1301-1315

1993

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Petrology and geochemistry at the Lower zone-Middle zone transition of the Panzhihua intrusion,SW China：Implications for differentiation and oxide ore genesis

Di xue qian yuan., 2013-09, Vol.4 (5), p.517-533

2013

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Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. 2. Effect of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology

Journal of medicinal chemistry, 1995-06, Vol.38 (12), p.2217-2230

1995

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Erratum: W.T. Stolle, J.A. Easter, M.J. Ackland, S.R. Haadsma-Svensson, C.-H. Lin, R.S.P. Hsi (1997). Synthesis of isotopically labeled CIS-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-(N-propyl)-1H]-benz[e]indole-9-carboxamide, a 5-HT1A receptor agonist. Journal of Labelled Compounds and Radiopharmaceuticals, Vol.XXXIX, No. 11, 891-900

Journal of labelled compounds & radiopharmaceuticals, 1998-01, Vol.41 (1), p.85-85

1998

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Synthesis and biological activity of cis-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-propyl-1H-benz[e]indole-9-carboxamide: A potent and selective 5-HT1A receptor agonist with good oral availability

Journal of medicinal chemistry, 1993-07, Vol.36 (15), p.2208-2218

1993

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Structure-Activity Relationships in the 8-Amino-6,7,8,9-tetrahydro-3H-benz[e]indole Ring System. Part 2: Effect of 8-Amino Nitrogen Substitution on Serotonin Receptor Binding and Pharmacology

Journal of medicinal chemistry, 1995-06, Vol.38 (12), p.2217-2230

1995

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Synthesis of isotopically labeled CIS-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-(N-propyl)-1H-benz[e]indole-9-carboxamide, a 5-HT1A receptor agonist

Journal of labelled compounds & radiopharmaceuticals, 1997-11, Vol.39 (11), p.891-900

1997

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Centrally acting serotonergic agents. Synthesis and structure-activity relationships of C-1- or C-3-substituted derivatives of 8-hydroxy-2-(di-n-propylamino)tetralin

Journal of medicinal chemistry, 1993-03, Vol.36 (6), p.671-682

1993

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Dopamine D 3 Receptor Antagonists. 1. Synthesis and Structure−Activity Relationships of 5,6-Dimethoxy- N -alkyl- and N -Alkylaryl-Substituted 2-Aminoindans

Journal of medicinal chemistry, 2001-12, Vol.44 (26), p.4716-4732

2001

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Comparison of childhood hepatic malignancies in a hepatitis B hyper-endemic area

World journal of gastroenterology : WJG, 2005-09, Vol.11 (34), p.5289

2005

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Alkynylation of alicyclic epoxides with alkynyldiethyl Alanes

Tetrahedron letters, 1969-01, Vol.10 (18), p.1379-1381

1969

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Erratum: W.T. Stolle, J.A. Easter, M.J. Ackland, S.R. Haadsma-Svensson, C.-H. Lin, R.S.P. Hsi (1997). Synthesis of isotopically labeled CIS-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-(N-propyl)-1H]-benz[e]indole-9-carboxamide, a 5-HT1A receptor agonist. Journal

Journal of labelled compounds & radiopharmaceuticals, 1998-01, Vol.41 (1), p.85-85

1998

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Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. II: Effects of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology

Journal of medicinal chemistry, 1995, Vol.38 (12), p.2217-2230

1995

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Centrally acting serotonergic and dopaminergic agents. 2. Synthesis and structure-activity relationships of 2,3,3a,4,9,9a-hexahydro-1H-benz[f]indole derivatives

Journal of medicinal chemistry, 1993-04, Vol.36 (8), p.1069-1083

1993

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Centrally acting serotonergic and dopaminergic agents. 1. Synthesis and structure-activity relationships of 2,3,3a,4,5,9b-hexahydro-1H-benz[e]indole derivatives

Journal of medicinal chemistry, 1993-04, Vol.36 (8), p.1053-1068

1993

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Synthesis and biological activity of C-5 modified derivatives of (+)-AJ76 and (+)-UH232: Increased dopamine D 3 receptor preference and improved pharmacokinetic properties

Bioorganic & medicinal chemistry letters, 1994, Vol.4 (5), p.689-694

1994

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Centrally acting serotonergic and dopaminergic agents. II: Synthesis and structure-activity relationships of 2,3,3a,4,9,9a-hexahydro-1H-benz[f]indole derivatives

Journal of medicinal chemistry, 1993, Vol.36 (8), p.1069-1083

1993

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Centrally acting serotonergic and dopaminergic agents. I: Synthesis and structure-activity relationships of 2,3,3a,4,5,9b-hexahydro-1H-benz[e]indole derivatives

Journal of medicinal chemistry, 1993, Vol.36 (8), p.1053-1068

1993

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substituted (S)-Phenylpiperidines and Rigid Congeners as Preferential Dopamine Autoreceptor Antagonists: Synthesis and Structure-Activity Relationships

Dopamine D3 Receptor Antagonists. 1. Synthesis and Structure−Activity Relationships of 5,6-Dimethoxy-N-alkyl- and N-Alkylaryl-Substituted 2-Aminoindans

C-9 and N-Substituted Analogs of cis-(3aR)-(-)-2,3,3a,4,5,9b-Hexahydro-3-propyl-1H-benz[e]indole-9-carboxamide: 5-HT1A Receptor Agonists with Various Degrees of Metabolic Stability

Synthesis and biological activity of C-5 modified derivatives of (+)-AJ76 and (+)-UH232 : increased dopamine D3 receptor preference and improved pharmacokinetic properties

Synthesis of (r)- and (s)-1-formyl-6,7,8,9-tetrahydro- N,N-(dipropyl)-3H-benz[e]indol-8-amines: Potent and orally active 5-ht1a receptor agonists

Benzindene prostaglandins. Synthesis of optically pure 15-deoxy-U-68,215 and its enantiomer via a modified intramolecular Wadsworth-Emmons-Wittig reaction

(Dipropylamino)-tetrahydronaphthofurans: centrally acting serotonin agonists and dopamine agonists-antagonists

Comparison of 5-HT1A and dopamine D2 pharmacophores. X-ray structures and affinities of conformationally constrained ligands

Petrology and geochemistry at the Lower zone-Middle zone transition of the Panzhihua intrusion,SW China：Implications for differentiation and oxide ore genesis

Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. 2. Effect of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology

Synthesis and biological activity of cis-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-propyl-1H-benz[e]indole-9-carboxamide: A potent and selective 5-HT1A receptor agonist with good oral availability

Structure-Activity Relationships in the 8-Amino-6,7,8,9-tetrahydro-3H-benz[e]indole Ring System. Part 2: Effect of 8-Amino Nitrogen Substitution on Serotonin Receptor Binding and Pharmacology

Synthesis of isotopically labeled CIS-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-(N-propyl)-1H-benz[e]indole-9-carboxamide, a 5-HT1A receptor agonist

Centrally acting serotonergic agents. Synthesis and structure-activity relationships of C-1- or C-3-substituted derivatives of 8-hydroxy-2-(di-n-propylamino)tetralin

Dopamine D 3 Receptor Antagonists. 1. Synthesis and Structure−Activity Relationships of 5,6-Dimethoxy- N -alkyl- and N -Alkylaryl-Substituted 2-Aminoindans

Comparison of childhood hepatic malignancies in a hepatitis B hyper-endemic area

Alkynylation of alicyclic epoxides with alkynyldiethyl Alanes

Erratum: W.T. Stolle, J.A. Easter, M.J. Ackland, S.R. Haadsma-Svensson, C.-H. Lin, R.S.P. Hsi (1997). Synthesis of isotopically labeled CIS-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-(N-propyl)-1H]-benz[e]indole-9-carboxamide, a 5-HT1A receptor agonist. Journal

Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. II: Effects of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology

Centrally acting serotonergic and dopaminergic agents. 2. Synthesis and structure-activity relationships of 2,3,3a,4,9,9a-hexahydro-1H-benz[f]indole derivatives

Centrally acting serotonergic and dopaminergic agents. 1. Synthesis and structure-activity relationships of 2,3,3a,4,5,9b-hexahydro-1H-benz[e]indole derivatives

Synthesis and biological activity of C-5 modified derivatives of (+)-AJ76 and (+)-UH232: Increased dopamine D 3 receptor preference and improved pharmacokinetic properties

Centrally acting serotonergic and dopaminergic agents. II: Synthesis and structure-activity relationships of 2,3,3a,4,9,9a-hexahydro-1H-benz[f]indole derivatives

Centrally acting serotonergic and dopaminergic agents. I: Synthesis and structure-activity relationships of 2,3,3a,4,5,9b-hexahydro-1H-benz[e]indole derivatives

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