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Anionic and zwitterionic copper(I) complexes incorporating an anionic N-heterocyclic carbene decorated with a malonate backbone: synthesis, structure and catalytic applications

Dalton transactions : an international journal of inorganic chemistry, 2013-01, Vol.42 (20), p.7373-7385

2013

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High-Efficacy 5-HT1A Agonists for Antidepressant Treatment: A Renewed Opportunity

Journal of medicinal chemistry, 2007-10, Vol.50 (20), p.5024-5033

2007

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Sodium Late Current Blockers in Ischemia Reperfusion: Is the Bullet Magic?

Journal of medicinal chemistry, 2008-07, Vol.51 (13), p.3856-3866

2008

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Radiosynthesis and preclinical evaluation of 18F-F13714 as a fluorinated 5-HT1A receptor agonist radioligand for PET neuroimaging

The Journal of nuclear medicine (1978), 2012-06, Vol.53 (6), p.969-976

2012

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3-(R)-[3-(2-methoxyphenylthio-2-(S)-methylpropyl]amino-3,4-dihydro-2H-1,5-benzoxathiepine bromhydrate (F 15845) prevents ischemia-induced heart remodeling by reduction of the intracellular Na+ overload

The Journal of pharmacology and experimental therapeutics, 2009-09, Vol.330 (3), p.696

2009

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Cellular BRET assay suggests a conformational rearrangement of preformed TrkB/Shc complexes following BDNF-dependent activation

Cellular signalling, 2010-01, Vol.22 (1), p.158-165

2010

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5-HT1A receptor activation and antidepressant-like effects : F 13714 has high efficacy and marked antidepressant potential

European journal of pharmacology, 2001-05, Vol.420 (2-3), p.103-112

2001

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F15599, a preferential post-synaptic 5-HT 1A receptor agonist: Activity in models of cognition in comparison with reference 5-HT 1A receptor agonists

European neuropsychopharmacology, 2010-09, Vol.20 (9), p.641-654

2010

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F15599, a preferential post-synaptic 5-HT1A receptor agonist: Activity in models of cognition in comparison with reference 5-HT1A receptor agonists

European neuropsychopharmacology, 2010-09, Vol.20 (9), p.641-654

2010

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A stereocontrolled access to 9-methyl cyclobuta[ a]indan: en route to rigid atipamezole analogues

Tetrahedron, 2011-09, Vol.67 (39), p.7598-7602

2011

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Cholecystocholedocholithiasis: a case–control study comparing the short- and long-term outcomes for a “laparoscopy-first” attitude with the outcome for sequential treatment (systematic endoscopic sphincterotomy followed by laparoscopic cholecystectomy)

Surgical endoscopy, 2010, Vol.24 (1), p.51-62

2010

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F15599, a highly selective post-synaptic 5-HT1A receptor agonist: in-vivo profile in behavioural models of antidepressant and serotonergic activity

The international journal of neuropsychopharmacology, 2010-11, Vol.13 (10), p.1285-1298

2010

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Design and Synthesis of a Series of 6-Substituted-2-pyridinylmethylamine Derivatives as Novel, High-Affinity, Selective Agonists at 5-HT1A Receptors

Journal of medicinal chemistry, 1998-12, Vol.41 (25), p.5070-5083

1998

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[18F]F15599, a novel 5-HT1A receptor agonist, as a radioligand for PET neuroimaging

European journal of nuclear medicine and molecular imaging, 2010-03, Vol.37 (3), p.594-605

2010

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Anti-inflammatory 17β-Thioalkyl-16α,17α-ketal and -acetal Androstanes: A New Class of Airway Selective Steroids for the Treatment of Asthma

Journal of medicinal chemistry, 1996-12, Vol.39 (25), p.4888-4896

1996

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Rigid Analogues of the α2-Adrenergic Blocker Atipamezole: Small Changes, Big Consequences

Journal of medicinal chemistry, 2010-10, Vol.53 (19), p.6986-6995

2010

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Radiosynthesis and Preclinical Evaluation of 18 F-F13714 as a Fluorinated 5-HT 1A Receptor Agonist Radioligand for PET Neuroimaging

Journal of Nuclear Medicine, 2012-06, Vol.53 (6), p.969-976

2012

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Radiosynthesis and Preclinical Evaluation of ^sup 18^F-F13714 as a Fluorinated 5-HT^sub 1A^ Receptor Agonist Radioligand for PET Neuroimaging

The Journal of nuclear medicine (1978), 2012-06, Vol.53 (6), p.969

2012

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Anionic and zwitterionic copper(i) complexes incorporating an anionic N-heterocyclic carbene decorated with a malonate backbone: synthesis, structure and catalytic applicationsElectronic supplementary information (ESI) available: NMR spectra of previously unknown compounds; perspective view of the cell packing of the structure of [2b]Li(thf)2. CCDC 912466912475. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c3dt32919d

2013-05

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Synthetic Studies on Cyclobuta[a]indanes: Stereocontrolled Access to C9-Substituted Derivatives

Journal of organic chemistry, 2009-01, Vol.74 (2), p.757-763

2009

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Preparation of Conformationally Constrained α 2 ‐Antagonists: The Bicyclo[3.2.0]heptane Approach

European journal of organic chemistry, 2006-01, Vol.2006 (1), p.246-256

2006

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Myocardial protection by F 15845, a persistent sodium current blocker, in an ischemia-reperfusion model in the pig

European journal of pharmacology, 2009-12, Vol.624 (1), p.16-22

2009

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Na+ Currents in Cardioprotection: Better to Be Late

Journal of medicinal chemistry, 2009-07, Vol.52 (14), p.4149-4160

2009

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Hyper-Raman Scattering: A Powerful Tool To Probe The Structure In Glasses

AIP conference proceedings, 2010, Vol.1267 (1), p.535-536

2010

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The invention of radical reactions part XVIII. A convenient solution to the 1-carbon problem (R-CO 2H → R- 13CO 2H)

Tetrahedron, 1988, Vol.44 (12), p.3501-3512

1988

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Anionic and zwitterionic copper(I) complexes incorporating an anionic N-heterocyclic carbene decorated with a malonate backbone: synthesis, structure and catalytic applications

High-Efficacy 5-HT1A Agonists for Antidepressant Treatment: A Renewed Opportunity

Sodium Late Current Blockers in Ischemia Reperfusion: Is the Bullet Magic?

Radiosynthesis and preclinical evaluation of 18F-F13714 as a fluorinated 5-HT1A receptor agonist radioligand for PET neuroimaging

3-(R)-[3-(2-methoxyphenylthio-2-(S)-methylpropyl]amino-3,4-dihydro-2H-1,5-benzoxathiepine bromhydrate (F 15845) prevents ischemia-induced heart remodeling by reduction of the intracellular Na+ overload

Cellular BRET assay suggests a conformational rearrangement of preformed TrkB/Shc complexes following BDNF-dependent activation

5-HT1A receptor activation and antidepressant-like effects : F 13714 has high efficacy and marked antidepressant potential

F15599, a preferential post-synaptic 5-HT 1A receptor agonist: Activity in models of cognition in comparison with reference 5-HT 1A receptor agonists

F15599, a preferential post-synaptic 5-HT1A receptor agonist: Activity in models of cognition in comparison with reference 5-HT1A receptor agonists

A stereocontrolled access to 9-methyl cyclobuta[ a]indan: en route to rigid atipamezole analogues

Cholecystocholedocholithiasis: a case–control study comparing the short- and long-term outcomes for a “laparoscopy-first” attitude with the outcome for sequential treatment (systematic endoscopic sphincterotomy followed by laparoscopic cholecystectomy)

F15599, a highly selective post-synaptic 5-HT1A receptor agonist: in-vivo profile in behavioural models of antidepressant and serotonergic activity

Design and Synthesis of a Series of 6-Substituted-2-pyridinylmethylamine Derivatives as Novel, High-Affinity, Selective Agonists at 5-HT1A Receptors

[18F]F15599, a novel 5-HT1A receptor agonist, as a radioligand for PET neuroimaging

Anti-inflammatory 17β-Thioalkyl-16α,17α-ketal and -acetal Androstanes: A New Class of Airway Selective Steroids for the Treatment of Asthma

Rigid Analogues of the α2-Adrenergic Blocker Atipamezole: Small Changes, Big Consequences

Radiosynthesis and Preclinical Evaluation of 18 F-F13714 as a Fluorinated 5-HT 1A Receptor Agonist Radioligand for PET Neuroimaging

Radiosynthesis and Preclinical Evaluation of ^sup 18^F-F13714 as a Fluorinated 5-HT^sub 1A^ Receptor Agonist Radioligand for PET Neuroimaging

Synthetic Studies on Cyclobuta[a]indanes: Stereocontrolled Access to C9-Substituted Derivatives

Preparation of Conformationally Constrained α 2 ‐Antagonists: The Bicyclo[3.2.0]heptane Approach

Myocardial protection by F 15845, a persistent sodium current blocker, in an ischemia-reperfusion model in the pig

Na+ Currents in Cardioprotection: Better to Be Late

Hyper-Raman Scattering: A Powerful Tool To Probe The Structure In Glasses

The invention of radical reactions part XVIII. A convenient solution to the 1-carbon problem (R-CO 2H → R- 13CO 2H)

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