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PET and SPECT imaging of the NMDA receptor system: an overview of radiotracer development

Mini reviews in medicinal chemistry, 2010-08, Vol.10 (9), p.870-886

2010

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Novel fluoroalkyl derivatives of selective kappa opioid receptor antagonist JDTic: Design, synthesis, pharmacology and molecular modeling studies

European journal of medicinal chemistry, 2015-01, Vol.90, p.742-750

2015

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N -[18 F]-FluoropropylJDTic for κ-Opioid Receptor PET Imaging: Radiosynthesis, Pre-clinical Evaluation, and Metabolic Investigation in Comparison with Parent JDTic

Nuclear medicine and biology, 2017-01, Vol.44, p.50-61

2017

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Oxidation of 2- and 3-Halogenated Quinolines: An Easy Access to 5- and 6-Halogenopyridine-2,3-dicarboxylic Acids

Synthesis (Stuttgart), 2004-08, Vol.2001 (16)

2004

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Oxidation of Aromatic Lithium Thiolates into Sulfinate Salts: An Attractive Entry to Aryl Sulfones Labeled with Carbon-11

Journal of organic chemistry, 2006-01, Vol.71 (1), p.210-214

2006

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[11 C]-MeJDTic: a novel radioligand for κ-opioid receptor positron emission tomography imaging

Nuclear medicine and biology, 2008-07, Vol.35 (5), p.561-569

2008

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Methyl transfer reaction from monomethyltin reagent under palladium(0) catalysis: a versatile method for labelling with carbon-11

Chemical communications (Cambridge, England), 2006-01 (1), p.97-99

2006

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Microspheres based on inulin for the controlled release of serine protease inhibitors: preparation, characterization and in vitro release

Journal of controlled release, 2003-09, Vol.92 (1), p.27-38

2003

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New synthesis of (Z,E)-2,7-bis(4-cyanobenzylidene)cycloheptan-1-one under stereospecific constraints induced by host-guest interactions

Chemical communications (Cambridge, England), 2005-08 (31), p.4007-4009

2005

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Lithiation of Functionalized Fluoroquinolines: Synthesis of Dihalo-2-phenylquinoline-4-carboxamides and in Vitro Evaluation as NK-3 Receptor Ligands for Medical Imaging Studies

Journal of organic chemistry, 2004-04, Vol.69 (7), p.2622-2625

2004

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Synthesis and Biological Evaluation of Halogenated Naphthyridone Carboxamides as Potential Ligands for in Vivo Imaging Studies of Substance P Receptors

Bioconjugate chemistry, 2003-05, Vol.14 (3), p.629-641

2003

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Syntheses of R and S isomers of AF-DX 384, a selective antagonist of muscarinic M 2 receptors

Bioorganic & medicinal chemistry, 2000-03, Vol.8 (3), p.591-600

2000

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Syntheses of R and S isomers of AF-DX 384, a selective antagonist of muscarinic M2 receptors

Bioorganic & medicinal chemistry, 2000-03, Vol.8 (3), p.591-600

2000

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ChemInform Abstract: Rapid Synthesis of Aliphatic Amides by Reaction of Carboxylic Acids, Grignard Reagent, and Amines: Application to the Preparation of [11C]Amides

ChemInform, 1998-02, Vol.29 (8), p.no-no

1998

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Reductive amination of carboxylic acids and [11C]magnesium halide carboxylates

Perkin 1 : an international journal of organic and bio-organic chemistry, 2000 (3), p.311-316

2000

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Synthesis and radiosynthesis with a positron emitter of EP 00652218, a potent antagonist of NK1 receptor, and of a fluoro analog for in vivo evaluation of the substance P receptor by pet

Journal of labelled compounds & radiopharmaceuticals, 2001-05, Vol.44 (S1), p.S283-S285

2001

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Radioiodinated analogs of EP 00652218 for the exploration of the tachykinin NK1 receptor by spect

Journal of labelled compounds & radiopharmaceuticals, 2001-05, Vol.44 (S1), p.S280-S282

2001

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ChemInform Abstract: Syntheses of Piperidine and Perhydroazepine Derivatives, Precursors of Two Selective Antagonists of Muscarinic M2 Receptors: AF-DX 384 and Its Perhydroazepine Isomer

ChemInform, 1997-05, Vol.28 (21), p.no-no

1997

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Syntheses of piperidine and perhydroazepine derivatives, precursors of two selective antagonists of muscarinic M2 receptors: AF-DX 384 and its perhydroazepine isomer

Journal of the Chemical Society, Perkin Transactions 1, 1996 (24), p.2925

1996

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Diastereoselective Syntheses of (3R,4R)- and (3R,4S)‑4-Aryl-3-methyl-4-piperidinemethanol and Fluoro Analogues

Journal of organic chemistry, 2013-02, Vol.78 (3), p.1222-1229

2013

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A Resin-Linker-Vector Approach to Radiopharmaceuticals Containing 18F: Application in the Synthesis of O-(2-[18F]-Fluoroethyl)-L-tyrosine

Chemistry : a European journal, 2013-01, Vol.19 (5), p.1720-1725

2013

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Remarkably Mild and Simple Preparation of Sulfenate Anions from β-Sulfinylesters: A New Route to Enantioenriched Sulfoxides

Journal of organic chemistry, 2005-04, Vol.70 (7), p.2812-2815

2005

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Rapid synthesis of quinoline-4-carboxylic acid derivatives from arylimines and 2-substituted acrylates or acrylamides under indium(III) chloride and microwave activations. Scope and limitations of the reaction

Organic & biomolecular chemistry, 2005-10, Vol.3 (20), p.3794-3804

2005

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A Resin-Linker-Vector Approach to Radiopharmaceuticals Containing $^{18}$F: Application in the Synthesis of O -(2-[ $^{18}$F]-Fluoroethyl)- L -tyrosine

Chemistry : a European journal, 2013-01, Vol.19, p.1720-1725

2013

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Cartographie simultanée de la vascularisation, de l’hypoxie et de la prolifération à l’aide de l’IRM de perfusion, la tep au 18f-fmiso et au 18f-flt, en relation avec la prise de contraste dans les glioblastomes

Journal of neuroradiology, 2021-06, Vol.48 (4), p.230-231

2021

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PET and SPECT imaging of the NMDA receptor system: an overview of radiotracer development

Novel fluoroalkyl derivatives of selective kappa opioid receptor antagonist JDTic: Design, synthesis, pharmacology and molecular modeling studies

N -[18 F]-FluoropropylJDTic for κ-Opioid Receptor PET Imaging: Radiosynthesis, Pre-clinical Evaluation, and Metabolic Investigation in Comparison with Parent JDTic

Oxidation of 2- and 3-Halogenated Quinolines: An Easy Access to 5- and 6-Halogenopyridine-2,3-dicarboxylic Acids

Oxidation of Aromatic Lithium Thiolates into Sulfinate Salts: An Attractive Entry to Aryl Sulfones Labeled with Carbon-11

[11 C]-MeJDTic: a novel radioligand for κ-opioid receptor positron emission tomography imaging

Methyl transfer reaction from monomethyltin reagent under palladium(0) catalysis: a versatile method for labelling with carbon-11

Microspheres based on inulin for the controlled release of serine protease inhibitors: preparation, characterization and in vitro release

New synthesis of (Z,E)-2,7-bis(4-cyanobenzylidene)cycloheptan-1-one under stereospecific constraints induced by host-guest interactions

Lithiation of Functionalized Fluoroquinolines: Synthesis of Dihalo-2-phenylquinoline-4-carboxamides and in Vitro Evaluation as NK-3 Receptor Ligands for Medical Imaging Studies

Synthesis and Biological Evaluation of Halogenated Naphthyridone Carboxamides as Potential Ligands for in Vivo Imaging Studies of Substance P Receptors

Syntheses of R and S isomers of AF-DX 384, a selective antagonist of muscarinic M 2 receptors

Syntheses of R and S isomers of AF-DX 384, a selective antagonist of muscarinic M2 receptors

ChemInform Abstract: Rapid Synthesis of Aliphatic Amides by Reaction of Carboxylic Acids, Grignard Reagent, and Amines: Application to the Preparation of [11C]Amides

Reductive amination of carboxylic acids and [11C]magnesium halide carboxylates

Synthesis and radiosynthesis with a positron emitter of EP 00652218, a potent antagonist of NK1 receptor, and of a fluoro analog for in vivo evaluation of the substance P receptor by pet

Radioiodinated analogs of EP 00652218 for the exploration of the tachykinin NK1 receptor by spect

ChemInform Abstract: Syntheses of Piperidine and Perhydroazepine Derivatives, Precursors of Two Selective Antagonists of Muscarinic M2 Receptors: AF-DX 384 and Its Perhydroazepine Isomer

Syntheses of piperidine and perhydroazepine derivatives, precursors of two selective antagonists of muscarinic M2 receptors: AF-DX 384 and its perhydroazepine isomer

Diastereoselective Syntheses of (3R,4R)- and (3R,4S)‑4-Aryl-3-methyl-4-piperidinemethanol and Fluoro Analogues

A Resin-Linker-Vector Approach to Radiopharmaceuticals Containing 18F: Application in the Synthesis of O-(2-[18F]-Fluoroethyl)-L-tyrosine

Remarkably Mild and Simple Preparation of Sulfenate Anions from β-Sulfinylesters: A New Route to Enantioenriched Sulfoxides

Rapid synthesis of quinoline-4-carboxylic acid derivatives from arylimines and 2-substituted acrylates or acrylamides under indium(III) chloride and microwave activations. Scope and limitations of the reaction

A Resin-Linker-Vector Approach to Radiopharmaceuticals Containing $^{18}$F: Application in the Synthesis of O -(2-[ $^{18}$F]-Fluoroethyl)- L -tyrosine

Cartographie simultanée de la vascularisation, de l’hypoxie et de la prolifération à l’aide de l’IRM de perfusion, la tep au 18f-fmiso et au 18f-flt, en relation avec la prise de contraste dans les glioblastomes

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