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Regioselective Rapid Analogue Syntheses of 1-Methyl-3,5-diarylpyrazoles via Palladium-catalysed Coupling to 3(5)-Pyrazolyl Nonaflates

Synlett, 2004-04, Vol.2004 (5), p.0795-0798

2004

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Synthesis of pyrido[2,3-d]pyridazines and pyrazino[2,3-d]-pyridazines—novel classes of GABAA receptor benzodiazepine binding site ligands

Tetrahedron letters, 2006-03, Vol.47 (13), p.2257-2260

2006

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Synthesis of pyrido[2,3- d]pyridazines and pyrazino[2,3- d]-pyridazines—novel classes of GABA A receptor benzodiazepine binding site ligands

Tetrahedron letters, 2006-03, Vol.47 (13), p.2257-2260

2006

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3-(4-Piperidinyl)- and 3-(8-aza-bicyclo[3.2.1]oct-3-yl)-2-phenyl-1h-indoles as bioavailable h5-HT2A antagonists

Bioorganic & medicinal chemistry letters, 2000-12, Vol.10 (24), p.2701-2703

2000

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Substituted pyrazoles as novel selective ligands for the human dopamine D4 receptor

Bioorganic & medicinal chemistry, 1998-10, Vol.6 (10), p.1731-1743

1998

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Substituted pyrazoles as novel selective ligands for the human dopamine D 4 receptor

Bioorganic & medicinal chemistry, 1998-10, Vol.6 (10), p.1731-1743

1998

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High-Affinity and Potent, Water-Soluble 5-Amino-1,4-benzodiazepine CCKB/Gastrin Receptor Antagonists Containing a Cationic Solubilizing Group

Journal of medicinal chemistry, 1994-03, Vol.37 (6), p.719-721

1994

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3-(4-Piperidinyl)- and 3-(8-aza-bicyclo[3.2.1]oct-3-yl)-2-phenyl-1 H-indoles as bioavailable h5-HT 2A antagonists

Bioorganic & medicinal chemistry letters, 2000, Vol.10 (24), p.2701-2703

2000

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4-Hydroxy-1-[3-(5-(1,2,4-triazol-4-yl)-1 H-indol-3-yl)propyl]piperidines: Selective h5-HT 1D agonists for the treatment of migraine

Bioorganic & medicinal chemistry letters, 1999, Vol.9 (23), p.3369-3374

1999

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4-Hydroxy-1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]piperidines : Selective h5-HT1D agonists for the treatment of migraine

Bioorganic & medicinal chemistry letters, 1999-12, Vol.9 (23), p.3369-3374

1999

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Carbamate Oxime Reduction: A New Route to C3-Amino-1,4-benzodiazepines

Synthesis (Stuttgart), 1994, Vol.1994 (5), p.505-508

1994

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Biological properties of the benzodiazepine amidine derivative L-740,093, a cholecystokinin-B/gastrin receptor antagonist with high affinity in vitro and high potency in vivo

Molecular pharmacology, 1994-11, Vol.46 (5), p.943-948

1994

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C5-piperazinyl-1,4-benzodiazepines, water-soluble, orally bioa vailable CCKB/gastrin receptor antagonists

Bioorganic & medicinal chemistry letters, 1995-12, Vol.5 (24), p.3023-3026

1995

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Regioselective Rapid Analogue Syntheses of 1-Methyl-3,5-diarylpyrazoles via Palladium-Catalyzed Coupling to 3(5)-Pyrazolyl Nonaflates

ChemInform, 2004-08, Vol.35 (33), p.no-no

2004

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C5-piperazinyl-1,4-benzodiazepines, water-soluble, orally bioa vailable CCK B/gastrin receptor antagonists

Bioorganic & medicinal chemistry letters, 1995, Vol.5 (24), p.3023-3026

1995

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Synthesis of Pyrido[2,3‐d]pyridazines and Pyrazino[2,3‐d]‐pyridazines — Novel Classes of GABA A Receptor Benzodiazepine Binding Site Ligands

ChemInform, 2006-07, Vol.37 (28)

2006

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Synthesis of Pyrido[2,3-d]pyridazines and Pyrazino[2,3-d]-pyridazines - Novel Classes of GABAA Receptor Benzodiazepine Binding Site Ligands

ChemInform, 2006-07, Vol.37 (28), p.no-no

2006

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ChemInform Abstract: 3-(4-Piperidinyl)- and 3-(8-Aza-bicyclo[3.2.1]oct-3-yl)-2-phenyl-1H-indoles as Bioavailable h5-HT2A Antagonists

ChemInform, 2001-03, Vol.32 (11), p.no-no

2001

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ChemInform Abstract: 3‐(4‐Piperidinyl)‐ and 3‐(8‐Aza‐bicyclo[3.2.1]oct‐3‐yl)‐2‐phenyl‐1H‐indoles as Bioavailable h5‐HT 2A Antagonists

ChemInform, 2001-03, Vol.32 (11)

2001

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ChemInform Abstract: 4-Hydroxyl-1- [3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]piperidines: Selective h5-HT1D Agonists for the Treatment of Migraine

ChemInform, 2000-02, Vol.31 (9), p.no-no

2000

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ChemInform Abstract: 4‐Hydroxyl‐1‐ [3‐(5‐(1,2,4‐triazol‐4‐yl)‐1H‐indol‐3‐yl)propyl]piperidines: Selective h5‐HT 1D Agonists for the Treatment of Migraine

ChemInform, 2000-02, Vol.31 (9)

2000

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Response to commentary by Drs. Poncet and Sénéchal

Clinical and experimental allergy, 2019-08, Vol.49 (8), p.1167-1168

2019

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Pru p 7 sensitization is a predominant cause of severe, cypress pollen‐associated peach allergy

Clinical and experimental allergy, 2019-04, Vol.49 (4), p.526-536

2019

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Can We Reduce Frame Rate to 15 Images per Second in Pediatric Videofluoroscopic Swallow Studies?

Dysphagia, 2020-04, Vol.35 (2), p.296-300

2020

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Saliva polymerase chain reaction assay for detection and follow-up of herpesvirus reactivation in patients with drug reaction with eosinophilia and systemic symptoms (DRESS)

JAMA dermatology (Chicago, Ill.), 2013-05, Vol.149 (5), p.565

2013

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Regioselective Rapid Analogue Syntheses of 1-Methyl-3,5-diarylpyrazoles via Palladium-catalysed Coupling to 3(5)-Pyrazolyl Nonaflates

Synthesis of pyrido[2,3-d]pyridazines and pyrazino[2,3-d]-pyridazines—novel classes of GABAA receptor benzodiazepine binding site ligands

Synthesis of pyrido[2,3- d]pyridazines and pyrazino[2,3- d]-pyridazines—novel classes of GABA A receptor benzodiazepine binding site ligands

3-(4-Piperidinyl)- and 3-(8-aza-bicyclo[3.2.1]oct-3-yl)-2-phenyl-1h-indoles as bioavailable h5-HT2A antagonists

Substituted pyrazoles as novel selective ligands for the human dopamine D4 receptor

Substituted pyrazoles as novel selective ligands for the human dopamine D 4 receptor

High-Affinity and Potent, Water-Soluble 5-Amino-1,4-benzodiazepine CCKB/Gastrin Receptor Antagonists Containing a Cationic Solubilizing Group

3-(4-Piperidinyl)- and 3-(8-aza-bicyclo[3.2.1]oct-3-yl)-2-phenyl-1 H-indoles as bioavailable h5-HT 2A antagonists

4-Hydroxy-1-[3-(5-(1,2,4-triazol-4-yl)-1 H-indol-3-yl)propyl]piperidines: Selective h5-HT 1D agonists for the treatment of migraine

4-Hydroxy-1-[3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]piperidines : Selective h5-HT1D agonists for the treatment of migraine

Carbamate Oxime Reduction: A New Route to C3-Amino-1,4-benzodiazepines

Biological properties of the benzodiazepine amidine derivative L-740,093, a cholecystokinin-B/gastrin receptor antagonist with high affinity in vitro and high potency in vivo

C5-piperazinyl-1,4-benzodiazepines, water-soluble, orally bioa vailable CCKB/gastrin receptor antagonists

Regioselective Rapid Analogue Syntheses of 1-Methyl-3,5-diarylpyrazoles via Palladium-Catalyzed Coupling to 3(5)-Pyrazolyl Nonaflates

C5-piperazinyl-1,4-benzodiazepines, water-soluble, orally bioa vailable CCK B/gastrin receptor antagonists

Synthesis of Pyrido[2,3‐d]pyridazines and Pyrazino[2,3‐d]‐pyridazines — Novel Classes of GABA A Receptor Benzodiazepine Binding Site Ligands

Synthesis of Pyrido[2,3-d]pyridazines and Pyrazino[2,3-d]-pyridazines - Novel Classes of GABAA Receptor Benzodiazepine Binding Site Ligands

ChemInform Abstract: 3-(4-Piperidinyl)- and 3-(8-Aza-bicyclo[3.2.1]oct-3-yl)-2-phenyl-1H-indoles as Bioavailable h5-HT2A Antagonists

ChemInform Abstract: 3‐(4‐Piperidinyl)‐ and 3‐(8‐Aza‐bicyclo[3.2.1]oct‐3‐yl)‐2‐phenyl‐1H‐indoles as Bioavailable h5‐HT 2A Antagonists

ChemInform Abstract: 4-Hydroxyl-1- [3-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)propyl]piperidines: Selective h5-HT1D Agonists for the Treatment of Migraine

ChemInform Abstract: 4‐Hydroxyl‐1‐ [3‐(5‐(1,2,4‐triazol‐4‐yl)‐1H‐indol‐3‐yl)propyl]piperidines: Selective h5‐HT 1D Agonists for the Treatment of Migraine

Response to commentary by Drs. Poncet and Sénéchal

Pru p 7 sensitization is a predominant cause of severe, cypress pollen‐associated peach allergy

Can We Reduce Frame Rate to 15 Images per Second in Pediatric Videofluoroscopic Swallow Studies?

Saliva polymerase chain reaction assay for detection and follow-up of herpesvirus reactivation in patients with drug reaction with eosinophilia and systemic symptoms (DRESS)

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