Joëlle Vidal
0000-0002-1542-2121
Université de Rennes 1
38 papers found
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Compounds useful as modulators of the proteasome activity
Electrophilic Amination of Amino Acids with N-Boc-oxaziridines: Efficient Preparation of N-Orthogonally Diprotected Hydrazino Acids and Piperazic Acid Derivatives
Process for the preparation of phenyl pyrazole compounds
Synthesis of Macrocyclic Peptide Analogues of Proteasome Inhibitor TMC-95A
N-Boc-3-trichloromethyloxaziridine: a new, powerful reagent for electrophilic amination
Design and Synthesis of Hydrazinopeptides and Their Evaluation as Human Leukocyte Elastase Inhibitors
N-Alkyloxycarbonyl-3-aryloxaziridines: Their Preparation, Structure, and Utilization As Electrophilic Amination Reagents
1. Nouveaux dérivés d’alpha-hydrazinoacides et procédé pour les fabriquer
Electrophilic amination reagents: A new method for the preparation of 3-Aryl-N-BOC (or N-FMOC) oxaziridines
Turn induction by N-aminoproline Comparison of the Gly-Pro-Gly and Glyψ[CO-NH-N]Pro-Gly sequences
Crystal structure analysis of a β-turn mimic in hydrazino peptides
Electrophilic amination: preparation and use of N-Boc-3-(4-cyanophenyl)oxaziridine, a new reagent that transfers a N-Boc group to N- and C-nucleophiles
Modifications of the amide bond and conformational constraints in pseudopeptide analogues
X-Ray conformational study of hydrazino peptide analogues
N-amination using N-methoxycarbonyl-3-phenyloxaziridine. Direct access to chiral Nβ-protected α-hydrazinoacids and carbazates
Synthesis of .alpha.-methylenecyclobutanones. First preparation of norsarkomycin methyl ester
Syntheses of nitrile and methyl ester corresponding to (dl)-sarkomycin and of related compounds
Use of alumina for elimination of sulfinic acid from β-aryl- and β-alkylsulfonyl carbonyl compounds.
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