130 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. Tuning the Regioselective Functionalization of Trifluoromethylated Dienes via Lanthanum‐Mediated Single C−F Bond Activation
16. Convergent Evolution of Diastereomeric Mixtures of 5-Methoxy-pentylzirconocenes toward Trans-1,2-substituted Cyclopentanes
17. Dual Activation of Unsaturated Amides with Schwartz's Reagent: A Diastereoselective Access to Cyclopentanols and N,O‐Dimethylcyclopentylhydroxylamines.
18. Broadening the reaction scope of unprotected aldosesviatheir corresponding nitrones: 1,3-dipolar cycloadditions with alkenes
19. 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
20. Aza-Henry Reaction with Nitrones, an Under-Explored Transformation
21. 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
22. Ring-Junction-Substituted Polyhydroxylated Pyrrolizidines and Indolizidines from Ketonitrone Cycloadditions
23. Synthesis of 1,3-disubstituted cyclohexenes from dienylethers via sequential hydrozirconation/deoxygenative cyclisation
24. Regiospecific formation of sugar-derived ketonitrone towards unconventional C-branched pyrrolizidines and indolizidines
25. Polyhydroxylated Quinolizidine Iminosugars as Nanomolar Selective Inhibitors of α-Glucosidases
26. Single or Synergistic Kinetic Resolutions of Chiral Allylalanes: Two Complementary Routes for the Asymmetric Synthesis of SynHomoallylamines
27. Broadening the reaction scope of unprotected aldoses via their corresponding nitrones: 1,3-dipolar cycloadditions with alkenes.
28. A second-generation ferrocene–iminosugar hybrid with improved fucosidase binding properties
29. Application of Elemental Lanthanides in the Selective C-F Activation of Trifluoromethylated Benzofulvenes Providing Access to Various Difluoroalkenes
30. Single or Synergistic Kinetic Resolutions of Chiral Allylalanes: Two Complementary Routes for the Asymmetric Synthesis of Syn Homoallylamines
31. Generation of ϵ,ϵ-Difluorinated Metal-Pentadienyl Species through Lanthanide-Mediated C−F Activation
32. 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 ?
33. Polyhydroxylated Quinolizidine Iminosugars as Nanomolar Selective Inhibitors of α-Glucosidases
34. Tetramethylammonium Fluoride
35. (+)-Camphor-mediated kinetic resolution of allylalanes: a strategy towards enantio-enriched cyclohex-2-en-1-ylalane
36. Biological activities of triterpenoids from Poraqueiba sericea stems
37. Perfluoroalkylation of Nitrones for the Synthesis of a Series of Fucosidase Inhibitors
38. Determination of the Relative Configuration and Conformational Analysis of Five-memberedN-Acyl-Iminosugars by Relevant3JCoupling Constants.
39. Exploring the divalent effect in fucosidase inhibition with stereoisomeric pyrrolidine dimers
40. Expanding the library of divalent fucosidase inhibitors with polyamino and triazole-benzyl bridged bispyrrolidines
41. Polyhydroxylated Quinolizidine Iminosugars as Nanomolar Selective Inhibitors of α-Glucosidases.
42. Hydroxymethyl-Branched Polyhydroxylated Indolizidines: Novel Selective α-Glucosidase Inhibitors
43. ChemInform Abstract: Perfluoroalkylation of Nitrones for the Synthesis of a Series of Fucosidase Inhibitors.
44. Synthesis of 2-carboxymethyl polyhydroxyazepanes and their evaluation as glycosidase inhibitors
45. Glycosidase inhibitors from the roots of Glyphaea brevis
46. Exploiting the Hydrophobic Terrain in Fucosidases with Aryl-Substituted Pyrrolidine Iminosugars
47. Biological activities of triterpenoids from Poraqueiba sericea stems.
48. Exploiting the Hydrophobic Terrain in Fucosidases with Aryl-Substituted Pyrrolidine Iminosugars.
49. Irreversible Inhibition of IspG, a Target for the Development of New Antimicrobials, by a 2-Vinyl Analogue of its MEcPP Substrate.
50. Dual Activation of Unsaturated Amides with Schwartz's Reagent: A Diastereoselective Access to Cyclopentanols and N,O-Dimethylcyclopentylhydroxylamines.
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