Jean-Bernard Behr

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

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

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

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

Chitin synthase, a fungal glycosyltransferase that is a valuable antifungal target.

Highly selective indium mediated allylation of unprotected pentosylamines.

Iminosugar-ferrocene conjugates as potential anticancer agents.

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

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

Exploiting the hydrophobic terrain in fucosidases with aryl-substituted pyrrolidine iminosugars.

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

Glycosidase inhibitors from the roots of Glyphaea brevis.

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

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

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

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

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