J. Paris

发表

Synthesis and evaluation of 1-(1H-indol-3-yl)ethanamine derivatives as new antibacterial agents.

D. Schneider, O. Burchak, T. Meinnel, 2011, Bioorganic & medicinal chemistry.

J. Paris, 2012 .

Electrochemical reduction of pristinamycin IA and related streptogramins in aqueous acidic medium

M. Vuilhorgne, N. Auzeil, J. Paris, 1994 .

Synthesis and activities of pyoverdin-quinolone adducts: a prospective approach to a specific Therapy against Pseudomonas aeruginosa.

M. Abdallah, J. Desnottes, J. Paris, 2001, Journal of medicinal chemistry.

Recent developments in streptogramin research.

J. Desnottes, S. Dutka-Malen, D. Beyer, 1998, Current pharmaceutical design.

Integrated Dataset of Screening Hits against Multiple Neglected Disease Pathogens

Simon Townson, Timothy Geary, Jean-Marc Paris, 2011, PLoS neglected tropical diseases.

Practical palladium-mediated deprotective method of Allyloxycarbonyl in aqueous media

E. Blart, M. Savignac, J. Paris, 1994 .

Synthesis and antimicrobial evaluation of amphiphilic neamine derivatives.

I. Baussanne, S. Halder, J. Décout, 2010, Journal of medicinal chemistry.

Palladium-catalyzed reactions in aqueous media. An efficient removal of allyloxycarbonyl protecting group from oxygen and nitrogen

E. Blart, M. Savignac, J. Genêt, 1993 .

Reactivity of 1-(des-3-hydroxy-picolinoyl) pristinamycin IA

J. Paris, J. Cassayre, E. Bacqué, 1998 .

Regio- and enantioselective synthesis of allylic fluorides by electrophilic fluorodesilylation of allyl silanes.

B. Greedy, V. Gouverneur, J. Paris, 2003, Angewandte Chemie.

Enantioselective organocatalytic route to trifluoromethyl-β-amino acids using chiral bases

J. Paris, J. Plaquevent, F. Metz, 2007 .

Stereoselective synthesis of trifluoromethyl-substituted 1,2-diamines by aza-Michael reaction with trans-3,3,3-trifluoro-1-nitropropene

C. Mioskowski, L. Lebeau, J. Paris, 2006 .

New progress in the cobalt-catalysed synthesis of aromatic organozinc compounds by reduction of aromatic halides by zinc dust

J. Paris, J. Périchon, C. Gosmini, 2003 .

1-Alkoxy-2,5-diphenylphospholane and -phospholanium Salts in Rhodium-Catalyzed Asymmetric Hydrogenation

J. Fiaud, R. Guillot, J. Paris, 2007 .

Antimicrobial activity against Staphylococcus aureus of semisynthetic injectable streptogramins: RP 59500 and related compounds.

D. Bouanchaud, J. Paris, J. Barrière, 1992, Journal of Antimicrobial Chemotherapy.

The Chemistry of Pristinamycins

J. Paris, P. Bost, J. Barrière, 1990 .

Stereoselective conjugate addition of nitrogen nucleophiles to 3,3,3-trifluoro-1-nitropropene

C. Mioskowski, L. Lebeau, J. Paris, 2006 .

Antitrypanosomal activity of 1,2-dihydroquinolin-6-ols and their ester derivatives.

L. Maes, Kiran V. Mahasenan, M. Kaiser, 2010, Journal of medicinal chemistry.

1‐(1H‐Indol‐3‐yl)ethanamine Derivatives as Potent Staphylococcus aureus NorA Efflux Pump Inhibitors

D. Schneider, O. Burchak, M. Jeanty, 2014, ChemMedChem.

Investigation of a series of silver-N-heterocyclic carbenes as antibacterial agents: activity, synergistic effects, and cytotoxicity.

Laure Eloy, T. Cresteil, S. Roland, 2011, Chemistry.

A novel transmetallation of arylzinc species into arylboronates from aryl halides in a barbier procedure.

J. Paris, J. Périchon, C. Gosmini, 2007, Chemical communications.

1-Alkoxy-2,5-diphenylphospholane and -phospholanium Salts in Rhodium-Catalyzed Asymmetric Hydrogenation.

J. Fiaud, R. Guillot, J. Paris, 2007 .

Intramolecular cyclopropanation of unsaturated terminal epoxides and chlorohydrins.

G. Freixas, J. Paris, D. M. Hodgson, 2007, Journal of the American Chemical Society.

Intramolecular cyclopropanation of unsaturated terminal epoxides.

J. Paris, D. M. Hodgson, Y. Chung, 2004, Journal of the American Chemical Society.

Unusual transformation of the 3-hydroxy-picolinoyl residue of pristinamycin IA.

M. Robin, M. Vuilhorgne, J. Paris, 1995, The Journal of antibiotics.

Preparation of des-3-hydroxy-picolinoyl pristinamycins I

M. Vuilhorgne, J. Paris, E. Bacqué, 1994 .

[Structure-activity relationship of semi-synthetic derivatives of the PIA component of pristinamycin].

D. Bouanchaud, J. Paris, J. Corbet, 1985, Pathologie-biologie.

2,2′-Bipyridine: An Efficient Ligand in the Cobalt-Catalyzed Synthesis of Organozinc Reagents from Aryl Chlorides and Sulfonates

J. Paris, J. Périchon, C. Gosmini, 2006 .

A Convenient Synthesis of 2,2-Diphenyl-Cyclohexanone and 6,6-Diphenyl-2-Cyclohexen-One

J. Paris, E. Bacqué, 1992 .

Enzymatic Transformations 63. High‐Concentration Two Liquid‐Liquid Phase Aspergillus niger Epoxide Hydrolase‐Catalysed Resolution: Application to Trifluoromethyl‐Substituted Aromatic Epoxides

R. Furstoss, J. Paris, F. Barbirato, 2007 .

Quick identification of kuraridin, a noncytotoxic anti-MRSA (methicillin-resistant Staphylococcus aureus) agent from Sophora flavescens using high-speed counter-current chromatography.

K. Fung, P. Leung, C. Lau, 2012, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

NEW DERIVATIVES OF 4,4-DIPHENYL-2-CYCLOHEXEN-ONE

J. Paris, J. Malleron, J. Peyronel, 1995 .

Convenient processes for the synthesis of aromatic ketones from aryl bromides and carboxylic anhydrides using a cobalt catalysis.

J. Paris, J. Périchon, C. Gosmini, 2004, The Journal of organic chemistry.

Palladium-Catalyzed Reactions of Aqueous Media. An Efficient Removal of Allyloxycarbonyl Protecting Group from Oxygen and Nitrogen.

E. Blart, M. Savignac, J. Genêt, 1993 .

Novel synthetic bis-indolic derivatives with antistaphylococcal activity, including against MRSA and VISA strains.

D. Schneider, O. Burchak, M. Maurin, 2015, The Journal of antimicrobial chemotherapy.

Enantioselective synthesis of girolline

J. Paris, A. Commerçon, 1991 .

C2 Arylated Benzo[b]thiophene Derivatives as Staphylococcus aureus NorA Efflux Pump Inhibitors

F. Popowycz, Carine Ganem-Elbaz, M. Lemaire, 2016, ChemMedChem.

Design and scalable synthesis of new chiral selectors. Part 1: Synthesis and characterization of a new constrained cyclopeptide from unnatural bulky amino acids

G. Coquerel, J. Paris, P. Cardinael, 2011 .

SYNTHESIS OF 3-AMINO 3-PHENYL AZETIDINE

J. Paris, E. Bacqué, S. L. Bitoux, 1995 .

Ethyl-4,4,4-trifluoroacetoacetate (ETFAA), a powerful building block for enantiopure chirons in trifluoromethyl-β-amino acid series

J. Paris, J. Plaquevent, F. Metz, 2007 .