A. Doutheau

发表

LuxR dependent quorum sensing inhibition by N,N'-disubstituted imidazolium salts.

L. Soulère, M. Sabbah, S. Reverchon, 2011, Bioorganic & medicinal chemistry.

Performance of Selected Microbial Pectinases on Synthetic Monomethyl-esterified Di- and Trigalacturonates*

J. Benen, J. Visser, V. Shevchik, 1999, The Journal of Biological Chemistry.

Synthesis and differential properties of creatine analogues as inhibitors for human creatine kinase isoenzymes.

J. Steghens, K. Min, C. Collombel, 1996, European journal of biochemistry.

Identification of the creatine binding domain of creatine kinase by photoaffinity labeling.

J. Steghens, K. Min, C. Collombel, 1998, Biochimica et biophysica acta.

Plasmalogens protect unsaturated lipids against UV-induced oxidation in monolayer.

M. Lagarde, S. Morandat, B. Roux, 2003, Biochimica et biophysica acta.

Differential membrane packing of stereoisomers of bis(monoacylglycero)phosphate.

M. Lagarde, Y. Hirano, Toshihide Kobayashi, 2006, Biochemistry.

Covalent binding of hydroxy-alkenals 4-HDDE, 4-HHE, and 4-HNE to ethanolamine phospholipid subclasses Published, JLR Papers in Press, February 16, 2003. DOI 10.1194/jlr.M200450-JLR200

M. Lagarde, B. Chantegrel, C. Deshayes, 2003, Journal of Lipid Research.

Quantitative structure-activity relationship for 4-hydroxy-2-alkenal induced cytotoxicity in L 6 muscle cells *

Bertrand R. Caré, L. Soulère, H. Soula, 2011 .

Quantitative structure-activity relationship for 4-hydroxy-2-alkenal induced cytotoxicity in L6 muscle cells.

Bertrand R. Caré, L. Soulère, H. Soula, 2010, Chemico-biological interactions.

Synthesis of transition-state analogues as potential inhibitors of sialidase from Influenza virus.

B. Barrère, G. Quash, P. Driguez, 1994, Carbohydrate research.

An expeditious synthesis of 4-hydroxy-2E-nonenal (4-HNE), its dimethyl acetal and of related compounds.

L. Soulère, Y. Queneau, A. Doutheau, 2007, Chemistry and physics of lipids.

A novel synthetic reversible inhibitor of sialidase efficiently blocks secondary but not primary influenza virus infection of MDCK cells in culture

B. Barrère, G. Quash, M. Aymard, 1997, Archives of Virology.

AHL signaling molecules with a large acyl chain enhance biofilm formation on sulfur and metal sulfides by the bioleaching bacterium Acidithiobacillus ferrooxidans

W. Sand, L. Soulère, C. Demergasso, 2013, Applied Microbiology and Biotechnology.

Contribution of 4-methylthio-2-oxobutanoate and its transaminase to the growth of methionine-dependent cells in culture. Effect of transaminase inhibitors.

B. Chantegrel, C. Deshayes, J. Chantepie, 1993, Biochemical pharmacology.

AHL signaling molecules with a large acyl chain enhance biofilm formation on sulfur and metal sulfides by the bioleaching bacterium Acidithiobacillus ferrooxidans

W. Sand, L. Soulère, C. Demergasso, 2013, Applied Microbiology and Biotechnology.

Carboxymethylglycoside lactones (CMGLs) : structural variations on the carbohydrate moiety

Y. Queneau, S. Chambert, A. Doutheau, 2007 .

Tandem mass spectrometric analysis of aspergillus niger pectin methylesterase: mode of action on fully methyl-esterified oligogalacturonates.

J. Benen, J. Visser, R. Orlando, 2000, The Biochemical journal.

Stereospecific 1,2 migration reactions during fluorination of 2-methoxy-2-methoxycarbonyl-3-hydroxytetrahydropyrans and the corresponding triflates

C. Deshayes, A. Doutheau, F. Cornille, 1990 .

The total synthesis of (+)-ryanodol. Part III. Preparation of (+)-anhydroryanodol from a key pentacyclic intermediate

A. Bélanger, C. Liao, J. Maffrand, 1990 .

The total synthesis of (+)-ryanodol. Part I. General strategy and search for a convenient diene for the construction of a key tricyclic intermediate

A. Bélanger, C. Liao, J. Maffrand, 1990 .

The total synthesis of (+)-ryanodol. Part II. Model studies for rings B and C of (+)-anhydroryanodol. Preparation of a key pentacyclic intermediate

A. Bélanger, C. Liao, J. Maffrand, 1990 .

The total synthesis of (+)-ryanodol. Part IV. Preparation of (+)-ryanodol from (+)-anhydroryanodol

A. Bélanger, C. Liao, J. Maffrand, 1990 .

Total synthesis of ryanodol

A. Bélanger, C. Liao, J. Maffrand, 1979 .

Rhodium carbenoid mediated cyclisation of a-diazo--keto-d-hydroxy-phenylsulfones

Françoise Léost, F. Lacrampe, A. Doutheau, 2000 .

Synthesis and Biological Evaluation of the Trifluoromethyl Analog of (4S)‐4,5‐Dihydroxy‐2,3‐pentanedione (DPD)

L. Soulère, D. Balestrino, C. Forestier, 2006 .

Synthesis of functionalized phenolic derivatives via the benzannulation of dienylketenes formed by a thermal wolff rearrangement of α-diazo-β-keto compounds

C. Deshayes, A. Doutheau, D. Collomb, 1996 .

Synthetic studies on the MARDi cascade: stereoselective synthesis of heterocyclic seven-membered rings.

Jean Rodriguez, Yoann Coquerel, A. Doutheau, 2006, Organic letters.

O-cyclisation of allenic β-ketoesters

T. Delair, A. Doutheau, 1986 .

Vinylketene-enamine cyclocondensation: a new access to functionalized phenols

A. Doutheau, D. Collomb, 1997 .

2-Phosphonocyclopenten-2-ones from ε-tert-butyldimethylsilyloxy-α-diazo-β-ketophosphonates via a rhodium(II)-catalysed C–H insertion reaction

A. Doutheau, W. Dayoub, Y. Diab, 2002 .

α-Phosphono-δ-lactones from γ-lactones via a rhodium(II)-catalysed Wolff rearrangement

A. Doutheau, W. Dayoub, Y. Diab, 2001 .

RADICAL CYCLISATION OF SOME 1,2,6-TRIDEOXY-3,4-DI-O-BENZYL-6-HALOGENO-L-ARABINO-HEX-1-YNITOL DERIVATIVES

M. Fontanel, A. Doutheau, Jean-Claude Malanda, 1991 .

Synthesis of new mono- and disaccharidic carboxymethylglycoside lactones (CMGLs) and their use toward 1,2-bisfunctionalized carbohydrate synthons

Y. Queneau, S. Chambert, A. Doutheau, 2008 .

AN EFFICIENT AND HIGHLY STEREOSELECTIVE ALPHA (14) GLYCOSYLATION BETWEEN TWO D-GALACTURONIC ACID ESTER DERIVATIVES

V. Shevchik, A. Doutheau, D. Magaud, 1997 .

Synthesis of sodium salt of ortho-(difluoromethyl)phenyl-α-ketoside of N-acetylneuraminic acid : a mechanism-based inhibitor of Clostridium perfringens neuraminidase.

B. Barrère, B. Chantegrel, C. Deshayes, 1992 .

5-exo-dig radical cyclisation of 1,2,6-trideoxy-6-iodo-L-arabino-hex-1-ynitols derivatives

A. Doutheau, Jean-Claude Malanda, 1993 .

Differential reactivity of alpha- and beta-anomers of glycosyl acceptors in glycosylations. A remote consequence of the endo-anomeric effect?

Y. Dory, P. Deslongchamps, A. Doutheau, 2000, Organic letters.

Heterocyclisations des hydroxy-6 methoxy-2 hexene-2 et heptene-2 oates de methyle.

A. Doutheau, C. Lila, A. Saroli, 1989 .

Preparation of functionalized cyclobutenones and phenolic compounds from α-diazo β-ketophosphonates

B. Chantegrel, C. Deshayes, A. Doutheau, 1993 .

Synthesis and Thermotropic Behavior of Simple New Glucolipid Amides

G. Mackenzie, J. Goodby, S. Cowling, 2007 .

SYNTHESIS OF α-FUNCTIONALIZED ALLENES

A. Saba, A. Doutheau, J. Goré, 1982 .

N-Sulfonyl homoserine lactones as antagonists of bacterial quorum sensing.

R. Haser, B. Chantegrel, C. Deshayes, 2004, Bioorganic & medicinal chemistry letters.

Preparation of new amide-linked pseudodisaccharides by the carboxymethylglycoside lactone (CMGL) strategy

Y. Queneau, S. Chambert, A. Doutheau, 2006 .

Carboxymethyl glucosides and carboxymethyl glucoside lactones: A detailed study of their preparation by oxidative degradation of disaccharides

Y. Queneau, S. Trombotto, S. Chambert, 2008 .

Synthesis of 9,9,9-trideutero-1,4-dihydroxynonane mercapturic acid (d3-DHN-MA), a useful internal standard for DHN-MA urinalysis

J. Steghens, B. Chantegrel, C. Deshayes, 2002, Lipids.

Ac2-DPD, the bis-(O)-acetylated derivative of 4,5-dihydroxy-2,3-pentanedione (DPD) is a convenient stable precursor of bacterial quorum sensing autoinducer AI-2.

L. Soulère, C. Deshayes, D. Balestrino, 2007, Bioorganic & medicinal chemistry letters.

Synthesis of the two monomethyl esters of the disaccharide 4-O-alpha-D-galacturonosyl-D-galacturonic acid and of precursors for the preparation of higher oligomers methyl uronated in definite sequences.

V. Shevchik, A. Doutheau, D. Magaud, 1998, Carbohydrate research.

Synthesis of methyl esters of 3-deoxy-d-erythro-2-hexulosonic acid (KDG) analogs, inducers of the expression of pectinase genes in bacteria Erwinia chrysanthemi

F. Alessi, G. Condemine, A. Doutheau, 1996 .

Malondialdehyde production from spermine by homogenates of normal and transformed cells.

G. Quash, L. Gazzolo, A. Doutheau, 1987, Biochimie.

(E) Enol ethers from the stereoselective reduction of α-alkoxy-β-ketophosphonates and Wittig type reaction

A. Doutheau, W. Dayoub, 2010 .

Highly Wolff Selective Rh(II) Catalysed Decomposition of α-Diazo- β-Ketophosphonates Having an Oxygen Atom Adjacent to the γ-Position

A. Doutheau, W. Dayoub, M. Boukraa, 2006 .

α-Phosphono-δ-lactones from γ-Lactones via a Rhodium(II)-Catalyzed Wolff Rearrangement.

A. Doutheau, W. Dayoub, Y. Diab, 2002 .

Synthesis of new methyl esters of 3-deoxy-d-erythro-2-hexulosonic acid (KDG) analogs, inducers of the expression of pectinase genes in bacteria Erwinia chrysanthemi

F. Alessi, G. Condemine, A. Doutheau, 1996 .

Trimethylsilylated 1,3-dienes or styrenes from the reaction between trimethylsilyldiazomethane and vinyl or aryl ketenes

Françoise Léost, A. Doutheau, 1999 .

N-Acyl-3-amino-5H-furanone derivatives as new inhibitors of LuxR-dependent quorum sensing: Synthesis, biological evaluation and binding mode study.

L. Soulère, Jane Estephane, S. Reverchon, 2008, Bioorganic & medicinal chemistry letters.

Evidence for in situ ethanolamine phospholipid adducts with hydroxy-alkenals Published, JLR Papers in Press, January 12, 2007.

M. Lagarde, B. Chantegrel, C. Deshayes, 2007, Journal of Lipid Research.

A Baylis–Hillman/ozonolysis route towards (±) 4,5-dihydroxy-2,3-pentanedione (DPD) and analogues

L. Soulère, Y. Queneau, A. Doutheau, 2005 .

Preparation of 1-Methoxycarbonyl-1-t-Butyldimethylsilyloxy Epoxides. Their Transformation into 3-Hydroxy 2-Acetal-Esters and certain 3-Hydroxy 2-Keto-Esters

P. Driguez, A. Doutheau, B. Pujol, 1992 .

A new route towards fimbrolide analogues: importance of the exomethylene motif in LuxR dependent quorum sensing inhibition

L. Soulère, M. Sabbah, Y. Queneau, 2013 .

AHL communication is a widespread phenomenon in biomining bacteria and seems to be involved in mineral-adhesion efficiency

W. Sand, L. Soulère, T. Rohwerder, 2008 .

Synthesis and biological evaluation of new N-acyl-homoserine-lactone analogues, based on triazole and tetrazole scaffolds, acting as LuxR-dependent quorum sensing modulators.

L. Soulère, M. Sabbah, Y. Queneau, 2012, Bioorganic & medicinal chemistry.

AHL-dependent quorum sensing inhibition: synthesis and biological evaluation of α-(N-alkyl-carboxamide)-γ-butyrolactones and α-(N-alkyl-sulfonamide)-γ-butyrolactones.

L. Soulère, M. Sabbah, Y. Queneau, 2011, Bioorganic & medicinal chemistry letters.

N-dibenzylphospho-N'-3-(2,6-dichlorophenyl)propyl-guanidine is a bisubstrate-analog for creatine kinase.

J. Steghens, K. Min, C. Collombel, 1997, Biochimica et biophysica acta.

The Total Synthesis of (+)-Ryanodol. Part 1. General Strategy and Search for a Convenient Diene for the Construction of a Key Tricyclic Intermediate.

A. Bélanger, C. Liao, J. Maffrand, 1990 .

Specific markers of lipid peroxidation issued from n-3 and n-6 fatty acids.

M. Lagarde, P. Molière, B. Chantegrel, 2004, Biochemical Society transactions.

A Baylis—Hillman/Ozonolysis Route Towards (.+-.) 4,5-Dihydroxy-2,3-pentanedione (DPD) and Analogues.

Laurent Soulère, Yves Queneau, L. Soulère, 2005 .

New synthetic analogues of N-acyl homoserine lactones as agonists or antagonists of transcriptional regulators involved in bacterial quorum sensing.

B. Chantegrel, C. Deshayes, S. Reverchon, 2002, Bioorganic & medicinal chemistry letters.

Synthetic homoserine lactone-derived sulfonylureas as inhibitors of Vibrio fischeri quorum sensing regulator.

L. Soulère, S. Reverchon, Y. Queneau, 2008, Bioorganic & medicinal chemistry.

LuxR-dependent quorum sensing: computer aided discovery of new inhibitors structurally unrelated to N-acylhomoserine lactones.

L. Soulère, M. Sabbah, Y. Queneau, 2010, Bioorganic & medicinal chemistry letters.

Molecular insights into quorum sensing in Acidithiobacillus ferrooxidans bacteria via molecular modelling of the transcriptional regulator AfeR and of the binding mode of long-chain acyl homoserine lactones

L. Soulère, Y. Queneau, C. Jerez, 2008, Journal of molecular modeling.

Exploring the active site of acyl homoserine lactones-dependent transcriptional regulators with bacterial quorum sensing modulators using molecular mechanics and docking studies.

L. Soulère, Y. Queneau, A. Doutheau, 2007, Journal of molecular graphics & modelling.

Synthesis and biological evaluation of homoserine lactone derived ureas as antagonists of bacterial quorum sensing.

L. Soulère, B. Chantegrel, C. Deshayes, 2006, Bioorganic & medicinal chemistry.

A New Synthesis of N-Acetyl-4-Deoxy-D-Neuraminic Acid

A. Doutheau, A. Saroli, G. Estenne, 1991 .

LuxR dependent quorum sensing inhibition by N,N'-disubstituted imidazolium salts.

L. Soulère, M. Sabbah, S. Reverchon, 2011, Bioorganic & medicinal chemistry.

LuxR-dependent quorum sensing: computer aided discovery of new inhibitors structurally unrelated to N-acylhomoserine lactones.

L. Soulère, M. Sabbah, Y. Queneau, 2010, Bioorganic & medicinal chemistry letters.

The effect of a novel inhibitor of aldehyde dehydrogenase on viral replication.

J. Chantepie, G. Quash, C. Marion, 1989, Biochemical pharmacology.