J. Behr

发表

Polyhydroxylated Quinolizidine Iminosugars as Nanomolar Selective Inhibitors of α-Glucosidases.

S. Py, A. Kanazawa, Anais Vieira Da Cruz, 2017, The Journal of organic chemistry.

Exploiting the Hydrophobic Terrain in Fucosidases with Aryl‐Substituted Pyrrolidine Iminosugars

G. Davies, J. Behr, D. W. Wright, 2015, Chembiochem : a European journal of chemical biology.

Structures of 5-Methylthioribose Kinase Reveal Substrate Specificity and Unusual Mode of Nucleotide Binding*

S. Ku, P. Howell, P. Yip, 2007, Journal of Biological Chemistry.

Expanding the library of divalent fucosidase inhibitors with polyamino and triazole-benzyl bridged bispyrrolidines.

J. Behr, Ana T. Carmona, I. Robina, 2016, Organic & biomolecular chemistry.

Spirocyclopropyl pyrrolidines as a new series of α-l-fucosidase inhibitors

R. Plantier-Royon, J. Behr, P. Vogel, 2006 .

Synthesis and l-fucosidase inhibitory activity of a new series of cyclic sugar imines—in situ formation and assay of their saturated counterparts

J. Behr, 2009 .

Convenient Synthesis of a Galacturonic Acid Based Macrocycle with Potential Copper-Complexation Ability

R. Plantier-Royon, J. Behr, L. Dupont, 2012 .

Synthesis and glycosidase inhibitory activity of 1-amino-3,6-anhydro-1-deoxy-D-sorbitol derivatives.

J. Behr, P. Vogel, Stéphane Guillarme, 2010, Bioorganic chemistry.

Generation of ϵ,ϵ-Difluorinated Metal-Pentadienyl Species through Lanthanide-Mediated C-F Activation.

J. Behr, Preethanuj Preethalayam, F. Jaroschik, 2017, Chemistry.

Synthesis, physico-chemical properties and complexing abilities of new amphiphilic ligands from D-galacturonic acid.

R. Plantier-Royon, J. Behr, V. Nardello‐Rataj, 2010, Carbohydrate research.

Thermodynamic and spectroscopic studies of Cu(II) and Ni(II) complexes with a new proline-threonine dipeptide ligand.

J. Behr, Z. Damaj, E. Guillon, 2008, Journal of inorganic biochemistry.

Trifluoromethide as a strong base: [CF3-] mediates dichloromethylation of nitrones by proton abstraction from the solvent.

R. Plantier-Royon, J. Behr, Dani Chavaria, 2013, The Journal of organic chemistry.

Aza-Henry Reaction with Nitrones, an Under-Explored Transformation

J. Behr, J. Vasse, F. Massicot, 2019, European Journal of Organic Chemistry.

Ti-Mediated Synthesis of Aminocyclopropyl-Substituted Carbohydrates

R. Plantier-Royon, J. Behr, P. Bertus, 2005 .

Synthesis and fucosidase inhibitory study of unnatural pyrrolidine alkaloid 4-epi-(+)-codonopsinine.

K. Robeyns, J. Behr, A. Kotland, 2011, The Journal of organic chemistry.

A concise synthesis of 2,5-dideoxy-2,5-imino-d-mannitol (DMDP) and HomoDMDP from l-xylose

J. Behr, G. Guillerm, 2007 .

Hydroxymethyl-Branched Polyhydroxylated Indolizidines: Novel Selective α-Glucosidase Inhibitors.

S. Py, J. Poisson, J. Behr, 2015, Organic letters.

Thermodynamic, spectroscopic studies and catechol oxidase activity of copper (II) complexes with amphiphilic d-galacturonic acid derived ligands

R. Plantier-Royon, J. Behr, L. Dupont, 2011 .

Synthesis of 1,3-disubstituted cyclohexenes from dienylethers via sequential hydrozirconation/deoxygenative cyclisation.

J. Behr, J. Vasse, Amandine Payet, 2019, Organic & biomolecular chemistry.

Design, synthesis and biological evaluation of hetaryl-nucleoside derivatives as inhibitors of chitin synthase.

J. Behr, G. Guillerm, T. Gourlain, 2003, Bioorganic & medicinal chemistry letters.

Broadening the reaction scope of unprotected aldoses via their corresponding nitrones: 1,3-dipolar cycloadditions with alkenes.

J. Behr, E. Riguet, Laura M. M. Pascual, 2020, Organic & biomolecular chemistry.

Ring‐Junction‐Substituted Polyhydroxylated Pyrrolizidines and Indolizidines from Ketonitrone Cycloadditions

S. Py, A. Kanazawa, J. Behr, 2018 .

Highly selective indium mediated allylation of unprotected pentosylamines.

J. Behr, A. Hottin, A. Ndoye, 2012, Organic letters.

Chiral N-dienyl-L-pyroglutamic esters in asymmetric hetero-Diels-Alder reactions with acylnitroso dienophiles

J. Behr, A. Defoin, J. Streith, 1996 .

Spiro Iminosugars: Structural Diversity and Synthetic Strategies

Damien Hazelard, Raphaël Hensienne, Jean-Bernard Behr, 2019, Topics in Heterocyclic Chemistry.

Single or Synergistic Kinetic Resolutions of Chiral Allylalanes: Two Complementary Routes for the Asymmetric Synthesis of Syn Homoallylamines.

J. Behr, F. Jaroschik, D. Harakat, 2017, Organic letters.

The spirocyclopropyl moiety as a methyl surrogate in the structure of l-fucosidase and l-rhamnosidase inhibitors.

R. Plantier-Royon, J. Behr, P. Vogel, 2009, Bioorganic & medicinal chemistry.

Asymmetric synthesis of potent glycosidase and very potent α-mannosidase inhibitors: 4-amino-4-deoxy-l-erythrose and 4-amino-4,5-dideoxy-l-ribose

J. Behr, C. Tarnus, A. Defoin, 2003 .

(±)-4-Amino-4,5-dideoxyribose, (±)-4-amino-4-deoxyerythrose, and (±)-dihydroxyproline derivatives from N-dienyl-γ-lactams

J. Behr, A. Defoin, N. Mahmood, 1995 .

(+)-Camphor-mediated kinetic resolution of allylalanes: a strategy towards enantio-enriched cyclohex-2-en-1-ylalane.

J. Behr, Jomy Joseph, F. Jaroschik, 2016, Chemical communications.

Homoallylic amines as efficient chiral inducing frameworks in the conjugate addition of amides to α,β-unsaturated esters. An entry to enantio-enriched diversely substituted amines.

J. Behr, J. Vasse, F. Massicot, 2020, Organic & biomolecular chemistry.

Synthesis of 6-deoxy-homoDMDP and its C(5)-epimer: absolute stereochemistry of natural products from Hyacinthus orientalis

J. Behr, G. Guillerm, 2002 .

Tandem nucleophilic addition/cyclization reaction in the synthesis of ketimine-type iminosugars.

R. Plantier-Royon, J. Behr, D. Harakat, 2008, The Journal of organic chemistry.

Glycosidase inhibitors from the roots of Glyphaea brevis.

J. Behr, D. Harakat, L. Voutquenne-Nazabadioko, 2015, Phytochemistry.

A Facile and Rapid Route to a New Series of Pyrrolizidines Structurally Related to (+)‐Alexine and (+)‐Australine

J. Behr, G. Guillerm, A. Erard, 2002 .

Inhibition of Chitin Synthetase from Saccharomyces cerevisiae by a New UDP-GlcNAc Analogue

J. Behr, N. Ryder, G. Guillerm, 2001, Journal of enzyme inhibition.

Synthesis of new (difluoromethylphosphono)azadisaccharides designed as bisubstrate analogue inhibitors for GlcNAc:beta-1,4 glycosyltransferases.

J. Behr, N. Ryder, G. Guillerm, 2000, Bioorganic & medicinal chemistry letters.

Synthesis of (difluoromethyl)phosphonate azasugars designed as inhibitors for glycosyl transferases

J. Behr, Ngan B. Phung, G. Guillerm, 1997 .

Perfluoroalkylation of Nitrones for the Synthesis of a Series of Fucosidase Inhibitors

R. Plantier-Royon, J. Behr, L. Dupont, 2015 .

α-L-fucosidase inhibition by pyrrolidine-ferrocene hybrids: rationalization of ligand-binding properties by structural studies.

C. Biot, G. Davies, J. Behr, 2013, Chemistry.

Iminosugar-ferrocene conjugates as potential anticancer agents.

C. Biot, J. Behr, P. Delannoy, 2012, Organic & biomolecular chemistry.

Iminosugars as glycosyltransferase inhibitors: synthesis of polyhydroxypyrrolidines and their evaluation on chitin synthase activity.

M. Muzard, J. Behr, G. Guillerm, 2005, European journal of medicinal chemistry.

Potent inhibition of chitin synthase by an azasugar—investigation of synergistic effect with UDP

J. Behr, Mounira Djebaili, 2005, Journal of enzyme inhibition and medicinal chemistry.

Chitin Synthase As an Antifungal Target: Recent Advances

J. Behr, 2003 .

Regiospecific formation of sugar-derived ketonitrone towards unconventional C-branched pyrrolizidines and indolizidines.

S. Py, J. Behr, J. Vasse, 2019, Organic & biomolecular chemistry.

Determination of the Relative Configuration and Conformational Analysis of Five–membered N-Acyl-Iminosugars by Relevant 3J Coupling Constants.

J. Behr, A. Defoin, Didier LeNouen, 2016 .

Short synthesis, X-ray and conformational analysis of a cyclic peracetylated L-sorbose-derived nitrone, a useful intermediate towards N–O-containing D-gluco-iminosugars

S. Py, A. Kanazawa, C. Philouze, 2018 .

Synthesis and glycosidase inhibition potency of all-trans substituted 1-C-perfluoroalkyl iminosugars.

R. Plantier-Royon, J. Behr, J. Vasse, 2018, Carbohydrate research.

Exploring the divalent effect in fucosidase inhibition with stereoisomeric pyrrolidine dimers.

G. Davies, J. Behr, D. W. Wright, 2016, Organic & biomolecular chemistry.

A second-generation ferrocene-iminosugar hybrid with improved fucosidase binding properties.

G. Davies, J. Behr, L. Duca, 2016, Bioorganic & medicinal chemistry letters.

Synthesis and l-fucosidase inhibitory potency of a cyclic sugar imine and its pyrrolidine analogue

R. Plantier-Royon, J. Behr, P. Vogel, 2008 .

Synthesis of 2-carboxymethyl polyhydroxyazepanes and their evaluation as glycosidase inhibitors.

R. Plantier-Royon, J. Behr, D. Harakat, 2015, Bioorganic chemistry.

Fmoc solid-phase synthesis of peptide thioesters using an intramolecularn,S-acyl shift.

O. Melnyk, J. Behr, N. Ollivier, 2005, Organic letters.

A dansyl-derivatized phytic acid analogue as a fluorescent substrate for phytases: experimental and computational approach.

C. Plassard, J. Behr, H. Quiquampoix, 2021, Bioorganic chemistry.

Biological activities of triterpenoids from Poraqueiba sericea stems

J. Behr, L. Duca, E. Rengifo, 2017, Natural product research.

The genus Poraqueiba ( Icacinaceae ) is composed of three species : Poraqueiba sericea Tulp

J. Behr, L. Duca, E. Rengifo, 2018 .

Convenient strategy for the synthesis of highly functionalizable hydroxylated unsaturated azepanes

R. Plantier-Royon, J. Behr, C. Portella, 2012 .

Convenient Strategy for the Synthesis of Highly Functionalizable Hydroxylated Unsaturated Azepanes.

R. Plantier-Royon, J. Behr, C. Portella, 2012 .

Inhibition of chitin synthase by a series of 7-deoxycasuarine stereoisomers designed as constrained analogues of the potent inhibitor 6-deoxyhomoDMDP

J. Behr, A. Gainvors-Claisse, A. Belarbi, 2006, Natural product research.

Spirocyclopropyl pyrrolidines as a new series of alpha-L-fucosidase inhibitors.

R. Plantier-Royon, J. Behr, P. Vogel, 2006, Bioorganic & medicinal chemistry.

Solid phase synthesis of mandelic acid-derived thioethers by α-keto carbocation trapping

O. Melnyk, J. Behr, J. Fruchart, 2004 .

Synthesis, Biological activities of chalcones and novel 4-acetylpyridine oximes, molecular docking of the synthesized products as acetylcholinesterase ligands

J. Behr, Kamilia Ould Lamara, Amina Benazzouz-touami, 2021, Journal of Molecular Structure.

Selectivity control in the reaction between 2-hydroxyarylaldehydes and 4-hydroxycoumarin. Antioxidant activities and computational studies of the formed products

J. Behr, Artur M. S. Silva, Malika Makhloufi-Chebli, 2021 .

Tuning the regioselective functionalization of trifluoromethylated dienes via lanthanum-mediated single C-F bond activation.

J. Behr, M. Taillefer, X. L. Le Goff, 2021, Chemistry.

Carbohydrate-Templated Syntheses of Trifluoromethyl-Substituted MEP Analogues for the Study of the Methylerythritol Phosphate Pathway.

J. Behr, P. Chaignon, Jean-Luc Vasse, 2023, The Journal of organic chemistry.

Protecting-group free synthesis of glycoconjugates displaying dual fungicidal and plant defense-eliciting activities.

J. Behr, J. Crouzet, Sandra Villaume, 2023, Bioorganic chemistry.