264 results on '"Behr, Jean-Bernard"'
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2. Synthesis, biological activities of chalcones and novel 4-acetylpyridine oximes, molecular docking of the synthesized products as acetylcholinesterase ligands
3. Selectivity control in the reaction between 2-hydroxyarylaldehydes and 4-hydroxycoumarin. Antioxidant activities and computational studies of the formed products
4. A dansyl-derivatized phytic acid analogue as a fluorescent substrate for phytases: experimental and computational approach
5. Kinetics of Strain-Promoted Alkyne-Nitrone Cycloadditions (SPANC) with Unprotected Carbohydrate Scaffolded Nitrones.
6. Spiro Iminosugars: Structural Diversity and Synthetic Strategies
7. Synthesis and glycosidase inhibition potency of all-trans substituted 1-C-perfluoroalkyl iminosugars
8. Carbohydrate-Templated Syntheses of Trifluoromethyl-Substituted MEP Analogues for the Study of the Methylerythritol Phosphate Pathway.
9. High-Pressure Activation to Circumvent Product Degradation in the Reaction of Unprotected Glyconitrones with Alkynes
10. High-Pressure Activation to Circumvent Product Degradation in the Reaction of Unprotected Glyconitrones with Alkynes.
11. Cover Feature: Irreversible Inhibition of IspG, a Target for the Development of New Antimicrobials, by a 2‐Vinyl Analogue of its MEcPP Substrate (Chem. Eur. J. 30/2022)
12. Irreversible Inhibition of IspG, a Target for the Development of New Antimicrobials, by a 2‐Vinyl Analogue of its MEcPP Substrate
13. Access to 5-bromopentanal and 6-bromohexanal derivatives via the bromination/hydrolysis of C,O-bis-zirconocenes generated from unsaturated Weinreb amides
14. Dual Activation of Unsaturated Amides with Schwartz's Reagent: A Diastereoselective Access to Cyclopentanols and N,O‐Dimethylcyclopentylhydroxylamines.
15. Thermodynamic, spectroscopic studies and catechol oxidase activity of copper (II) complexes with amphiphilic d-galacturonic acid derived ligands
16. Synthesis, physico-chemical properties and complexing abilities of new amphiphilic ligands from d-galacturonic acid
17. The spirocyclopropyl moiety as a methyl surrogate in the structure of l-fucosidase and l-rhamnosidase inhibitors
18. Thermodynamic and spectroscopic studies of Cu(II) and Ni(II) complexes with a new proline–threonine dipeptide ligand
19. Synthesis and l-fucosidase inhibitory potency of a cyclic sugar imine and its pyrrolidine analogue
20. Tuning the Regioselective Functionalization of Trifluoromethylated Dienes via Lanthanum‐Mediated Single C−F Bond Activation
21. Convergent Evolution of Diastereomeric Mixtures of 5-Methoxy-pentylzirconocenes toward Trans-1,2-substituted Cyclopentanes
22. Dual Activation of Unsaturated Amides with Schwartz's Reagent: A Diastereoselective Access to Cyclopentanols and N,O‐Dimethylcyclopentylhydroxylamines.
23. Spirocyclopropyl pyrrolidines as a new series of α- l-fucosidase inhibitors
24. Broadening the reaction scope of unprotected aldosesviatheir corresponding nitrones: 1,3-dipolar cycloadditions with alkenes
25. 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
26. Iminosugars as glycosyltransferase inhibitors: synthesis of polyhydroxypyrrolidines and their evaluation on chitin synthase activity
27. Aza-Henry Reaction with Nitrones, an Under-Explored Transformation
28. 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
29. 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
30. Ring-Junction-Substituted Polyhydroxylated Pyrrolizidines and Indolizidines from Ketonitrone Cycloadditions
31. Synthesis of 1,3-disubstituted cyclohexenes from dienylethers via sequential hydrozirconation/deoxygenative cyclisation
32. Regiospecific formation of sugar-derived ketonitrone towards unconventional C-branched pyrrolizidines and indolizidines
33. Polyhydroxylated Quinolizidine Iminosugars as Nanomolar Selective Inhibitors of α-Glucosidases
34. Single or Synergistic Kinetic Resolutions of Chiral Allylalanes: Two Complementary Routes for the Asymmetric Synthesis of SynHomoallylamines
35. Broadening the reaction scope of unprotected aldoses via their corresponding nitrones: 1,3-dipolar cycloadditions with alkenes.
36. A second-generation ferrocene–iminosugar hybrid with improved fucosidase binding properties
37. Application of Elemental Lanthanides in the Selective C-F Activation of Trifluoromethylated Benzofulvenes Providing Access to Various Difluoroalkenes
38. Single or Synergistic Kinetic Resolutions of Chiral Allylalanes: Two Complementary Routes for the Asymmetric Synthesis of Syn Homoallylamines
39. Generation of ϵ,ϵ-Difluorinated Metal-Pentadienyl Species through Lanthanide-Mediated C−F Activation
40. Projet ANR- 11-BSV7-015 01 - UNLOCKP – Mobilisation des réserves de Phytate du sol : quelles sont les clefs nécessaires pour accéder au phosphore de ce trésor ?
41. Tandem nucleophilic addition/cyclization reaction in the synthesis of ketimine-type iminosugars
42. Polyhydroxylated Quinolizidine Iminosugars as Nanomolar Selective Inhibitors of α-Glucosidases
43. Tetramethylammonium Fluoride
44. (+)-Camphor-mediated kinetic resolution of allylalanes: a strategy towards enantio-enriched cyclohex-2-en-1-ylalane
45. Biological activities of triterpenoids from Poraqueiba sericea stems
46. Perfluoroalkylation of Nitrones for the Synthesis of a Series of Fucosidase Inhibitors
47. Determination of the Relative Configuration and Conformational Analysis of Five-memberedN-Acyl-Iminosugars by Relevant3JCoupling Constants.
48. Exploring the divalent effect in fucosidase inhibition with stereoisomeric pyrrolidine dimers
49. Expanding the library of divalent fucosidase inhibitors with polyamino and triazole-benzyl bridged bispyrrolidines
50. Polyhydroxylated Quinolizidine Iminosugars as Nanomolar Selective Inhibitors of α-Glucosidases.
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