C. Perrio

发表

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

M. Prud'homme, I. Dez, M. Lasne, 2003, Journal of controlled release : official journal of the Controlled Release Society.

N-[18F]-FluoropropylJDTic for κ-opioid receptor PET imaging: Radiosynthesis, pre-clinical evaluation, and metabolic investigation in comparison with parent JDTic.

J. Delamare, C. Perrio, O. Tirel, 2017, Nuclear medicine and biology.

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

L. Barré, G. Poisnel, D. Debruyne, 2008, Nuclear medicine and biology.

Hypoxia Imaging and Adaptive Radiotherapy: A State-of-the-Art Approach in the Management of Glioma

B. Dubray, M. Bernaudin, S. Valable, 2019, Front. Med..

[18F]-Fluoride capture and release: azeotropic drying free nucleophilic aromatic radiofluorination assisted by a phosphonium borane.

F. Gabbaï, C. Perrio, D. Pla, 2016, Chemical communications.

A Resin-linker-vector approach to radiopharmaceuticals containing 18F: application in the synthesis of O-(2-[18F]-fluoroethyl)-L-tyrosine.

V. Isoni, Neil J Wells, H. Wadsworth, 2013, Chemistry.

Copper-catalyzed amination of (bromophenyl)ethanolamine for a concise synthesis of aniline-containing analogues of NMDA NR2B antagonist ifenprodil.

L. Barré, A. Buisson, P. Marchand, 2010, Organic & biomolecular chemistry.

Deoxyradiofluorination Reaction from β-Hydroxy-α-aminoesters: an Entry to [18 F]Fluoroaminoesters under Mild Conditions

C. Perrio, F. Gourand, M. Morlot, 2019, European Journal of Organic Chemistry.

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

C. Perrio, S. Schmitt, N. Colloc’h, 2015, European journal of medicinal chemistry.

GluN2B Subunit Labeling with Fluorescent Probes and High-Resolution Live Imaging.

A. Buisson, O. Nicole, C. Perrio, 2017, Methods in molecular biology.

Confocal microscopy imaging of NR2B-containing NMDA receptors based on fluorescent ifenprodil-like conjugates.

Laetitia Mony, P. Paoletti, L. Barré, 2012, Bioconjugate chemistry.

Synthesis and biological evaluation of novel fluoro and iodo quinoline carboxamides as potential ligands of NK-3 receptors for in vivo imaging studies.

L. Barré, I. Bennacef, M. Lasne, 2004, Bioorganic & medicinal chemistry.

The first radiosynthesis of 2-amino-5-[18F]fluoropyridines via a "minimalist" radiofluorination/palladium-catalyzed amination sequence from anisyl(2-bromopyridinyl)iodonium triflate.

C. Aubert, C. Perrio, G. Bluet, 2019, Organic & biomolecular chemistry.

Development, Optimization, and Scope of the Radiosynthesis of 3/5-[18F]Fluoropyridines from Readily Prepared Aryl(pyridinyl) Iodonium Salts: The Importance of TEMPO and K2CO3

C. Aubert, C. Perrio, G. Bluet, 2019, Organic Process Research & Development.

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

L. Barré, F. Sobrio, C. Perrio, 2010, Mini reviews in medicinal chemistry.

Evaluation of Specific Binding of [11C]RTI-97 to Kappa Opioid Receptor by Autoradiography and PET Imaging in Rat.

M. Ibazizène, F. Noble, C. Perrio, 2021, ACS medicinal chemistry letters.

Sultone opening with [18F]fluoride: an efficient 18F-labelling strategy for PET imaging.

L. Barré, C. Perrio, S. Schmitt, 2011, Chemical communications.

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

L. Barré, M. Huiban, F. Sobrio, 2006, Chemical communications.

Oxidation of aromatic lithium thiolates into sulfinate salts: an attractive entry to aryl sulfones labeled with carbon-11.

M. Lasne, C. Perrio, S. Perrio, 2006, The Journal of organic chemistry.

Chemistry of β +-Emitting Compounds Based on Fluorine-18

C. Crouzel, L. Barré, F. Dollé, 2002 .

Lithiation of functionalized fluoroquinolines: synthesis of dihalo-2-phenylquinoline-4-carboxamides and in vitro evaluation as NK-3 receptor ligands for medical imaging studies.

L. Barré, I. Bennacef, M. Lasne, 2004, The Journal of organic chemistry.

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.

O. Parisel, M. Lasne, C. Perrio, 2005, Organic & biomolecular chemistry.

Diastereoselective conjugate addition of organocuprates to 3,4-dimethyl-5,6-dihydro-2(1H)-pyridinones. A concise synthesis of trans-3,4-dimethyl-4-phenylpiperidines.

L. Barré, C. Perrio, G. Dupas, 2007, Organic letters.

Chemical delivery system of metaiodobenzylguanidine (MIBG) to the central nervous system.

M. Ibazizène, L. Barré, J. Henry, 2010, Journal of medicinal chemistry.

Synthesis and in Vitro Characterisation of Ifenprodil‐Based Fluorescein Conjugates as GluN1/GluN2B N‐Methyl‐D‐aspartate Receptor Antagonists

E. Mackenzie, L. Barré, A. Buisson, 2013, Chembiochem : a European journal of chemical biology.

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

S. Petit, G. Coquerel, G. Gouhier, 2005, Chemical communications.

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

F. Dauphin, P. Desbène, C. Morin, 2000, Bioorganic & Medicinal Chemistry.

Simultaneous Mapping of Vasculature, Hypoxia, and Proliferation Using Dynamic Susceptibility Contrast MRI, 18F-FMISO PET, and 18F-FLT PET in Relation to Contrast Enhancement in Newly Diagnosed Glioblastoma

M. Hatt, D. Visvikis, M. Bernaudin, 2021, The Journal of Nuclear Medicine.

Functionalization through lithiation of (S)-N-(1-phenylpropyl)-2-phenylquinoline-4-carboxamide. Application to the labeling with carbon-11 of NK-3 receptor antagonist SB 222200.

L. Barré, I. Bennacef, M. Lasne, 2007, The Journal of organic chemistry.

Pd(0)-Catalyzed Direct C-H Functionalization of 2-H-4-Benzylidene Imidazolones: Friendly and Large-Scale Access to GFP and Kaede Protein Fluorophores.

C. Hoarau, C. Perrio, L. Bischoff, 2016, Chemistry.

Multimodal evaluation of hypoxia in brain metastases of lung cancer and interest of hypoxia image-guided radiotherapy

M. Bernaudin, S. Valable, F. Chapon, 2021, Scientific Reports.

Synthesis and biological evaluation of halogenated naphthyridone carboxamides as potential ligands for in vivo imaging studies of substance P receptors.

L. Barré, D. Guilloteau, P. Emond, 2003, Bioconjugate chemistry.

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

L. Barré, D. Guilloteau, F. Dauphin, 2001 .

Diastereoselective syntheses of (3R*,4R*)- and (3R*,4S*)-4-aryl-3-methyl-4-piperidinemethanol and fluoro analogues.

Richard C. D. Brown, C. Perrio, S. Schmitt, 2013, The Journal of organic chemistry.

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

L. Barré, D. Guilloteau, F. Dauphin, 2001 .