32 research outputs found
(E) Enol ethers from the stereoselective reduction of α-alkoxy-β-ketophosphonates and Wittig type reaction
International audienc
(E) Enol ethers from the stereoselective reduction of α-alkoxy-β-ketophosphonates and Wittig type reaction
International audienc
Highly Wolff selective Rh(II) catalysed decomposition of alpha-diazo-beta-ketophosphonates having an oxygen atom adjacent to the gama-position
International audienc
Oxidation of coupled vinylallenes as a method of synthesis of cyclopentenone derivatives
Preparation of amide-linked pseudo-disaccharides by the carboxymethylglycoside lactone (CMGL) strategy
International audienc
Synthetic Studies on the MARDI Cascade : Stereoselective Synthesis of Heterocyclic Seven-Membered
International audienc
Bis-(O)-acetylated derivative of 4,5-dihydroxy-2,3-pentanedione (DPD): a convenient stable precursor of quorum sensing autoinducer AI-2
International audienc
Mechanisms and synthetic modulators of AHL-dependent gene regulation.
International audienc
N-Acyl-3-amino-5H-furanone derivatives as new inhibitors of LuxR-dependent quorum sensing: Synthesis, biological evaluation and binding mode study
Synthetic homoserine lactone-derived sulfonylureas as inhibitors of Vibrio fischeri quorum sensing regulator
International audienceA series of 9 homoserine lactone-derived sulfonylureas substituted by an alkyl chain, some of them bearing a phenyl group at the extremity, have been prepared. All compounds were found to inhibit the action of 3-oxo-hexanoyl-l-homoserine lactone, the natural inducer of bioluminescence in the bacterium Vibrio fischeri, the aliphatic compounds being more active than their phenyl-substituted counterparts. Molecular modelling studies performed on the most active compound in each series suggest that the antagonist activity could be related to the perturbation of the hydrogen-bond network in the ligand–protein complexes