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Téléphone
05 40 00 64 49
Groupe de recherche
CESAMO
Statut
Permanent
Poste
ITA/BIATSS
Batiment
A12
Etage
2° Est
Publications
Revisiting the mechanism responsible for the light-struck flavor in white wines and Champagnes. In Food Chemistry (Vol. 372, p. 131281). https://doi.org/10.1016/j.foodchem.2021.131281
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Development of a Solid-Phase Microextraction-Gas Chromatography/Mass Spectrometry Method for Quantifying Nitrogen-Heterocyclic Volatile Aroma Compounds: Application to Spirit and Wood Matrices. In Journal of Agricultural and Food Chemistry (Vol. 67, Issue 49, p. 13694-13705). https://doi.org/10.1021/acs.jafc.9b05716
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Benzophenone vs. Copper/Benzophenone in Light-Promoted Atom Transfer Radical Additions (ATRAs): Highly Effective Iodoperfluoroalkylation of Alkenes/Alkynes and Mechanistic Studies. In Advanced Synthesis and Catalysis (Vol. 358, Issue 18, p. 2949-2961). https://doi.org/10.1002/adsc.201600501
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Isolation, characterization, and determination of a new compound in red wine. In Analytical and Bioanalytical Chemistry (Vol. 406, Issue 4, p. 1201-1208). https://doi.org/10.1007/s00216-013-7244-z
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Impact of ethanol content on the scavenging activities of oak wood C-glycosidic ellagitannins. Application to the evaluation of the nutritional status of spirits. In Journal of the Institute of Brewing (Vol. 119, Issue 3, p. 116-125). https://doi.org/10.1002/jib.70
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Degradation pathways of holocellulose, lignin and α-cellulose from Pteris vittata fronds in sub- and super critical conditions. In Biomass and Bioenergy (Vol. 43, p. 65-71). https://doi.org/10.1016/j.biombioe.2012.03.035
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Accumulation of total lipids, fatty acids and triacylglycerols in developing fruits of Olea europaea L.. In Scientia Horticulturae (Vol. 132, Issue 1, p. 7-11). https://doi.org/10.1016/j.scienta.2011.07.025
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Dendritic carrier based on PEG: Design and degradation of acid-sensitive dendrimer-like poly(ethylene oxide)s. In Macromolecular Rapid Communications (Vol. 32, Issue 21, p. 1722-1728). https://doi.org/10.1002/marc.201100459
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Optical performances degradation of InGaN/GaN MQW LEDs related to fluorescence shift of copolymer-based silicone coating. In Proceedings of SPIE - The International Society for Optical Engineering (Vol. 8123, p. 81230G). https://doi.org/10.1117/12.893528
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Carbocationic polymerization of isoprene Co-initiated by B(C 6 F5 )3 : An alternative route toward natural rubber polymer analogues?. In Macromolecules (Vol. 44, Issue 6, p. 1372-1384). https://doi.org/10.1021/ma1027966
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Ferrocenyl-terminated redox stars: Synthesis and electrostatic effects in mixed-valence stabilization. In Journal of the American Chemical Society (Vol. 133, Issue 3, p. 629-641). https://doi.org/10.1021/ja109380u
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New strategies to study the chemical nature of wine oligomeric procyanidins. In Analytical and Bioanalytical Chemistry (Vol. 401, Issue 5, p. 1489-1499). https://doi.org/10.1007/s00216-011-4988-1
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A kinetic study of the reaction of (+)-catechin and malvidin-3-glucoside with aldehydes derived from toasted oak. In Natural Products Journal (Vol. 1, Issue 1, p. 47-56). https://doi.org/10.2174/2210316311101010047
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Conversion of fern (Pteris vittata L.) biomass from a phytoremediation trial in sub- and supercritical water conditions. In Biomass and Bioenergy (Vol. 35, Issue 2, p. 872-883). https://doi.org/10.1016/j.biombioe.2010.11.007
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Characterisation and accumulation of squalene and n-alkanes in developing Tunisian Olea europaea L. fruits. In International Journal of Food Science and Technology (Vol. 46, Issue 11, p. 2281-2286). https://doi.org/10.1111/j.1365-2621.2011.02747.x
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Study by LC/ESI/MSn and ESI/HR/MS of SO2 interactions in flavanols-aldehydes nucleophilic reactions. In Food Chemistry (Vol. 122, Issue 3, p. 488-494). https://doi.org/10.1016/j.foodchem.2009.08.029
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Precision synthesis and characterization of thymine-functionalized polyisobutylene. In Journal of Polymer Science, Part A: Polymer Chemistry (Vol. 48, Issue 16, p. 3501-3506). https://doi.org/10.1002/pola.24058
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Comparative analysis of triacylglycerols from Olea europaea L. fruits using HPLC and MALDI-TOFMS. In European Journal of Lipid Science and Technology (Vol. 112, Issue 5, p. 574-579). https://doi.org/10.1002/ejlt.200900079
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Policosanol characterization and accumulation during ripening of Tunisian Olea europaea L. fruits. In European Journal of Lipid Science and Technology (Vol. 112, Issue 3, p. 373-379). https://doi.org/10.1002/ejlt.200900076
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Lipid components of olive oil from Tunisian Cv. Sayali: Characterization and authenticity. In Comptes Rendus - Biologies (Vol. 333, Issue 9, p. 642-648). https://doi.org/10.1016/j.crvi.2010.05.001
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N-Heterocyclic carbene-organocatalyzed ring-opening polymerization of ethylene oxide in the presence of alcohols or trimethylsilyl nucleophiles as chain moderators for the synthesis of α,ω-heterodifunctionalized poly(ethylene oxide)s. In Macromolecules (Vol. 43, Issue 6, p. 2814-2823). https://doi.org/10.1021/ma902676r
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Gas chromatographic-mass spectrometric characterisation of triterpene alcohols and monomethylsterols in developing Olea europaea L. fruits. In Food Chemistry (Vol. 116, Issue 1, p. 345-350). https://doi.org/10.1016/j.foodchem.2009.01.094
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Main-chain fullerene polymers for photovoltaic devices. In Macromolecules (Vol. 42, Issue 10, p. 3549-3558). https://doi.org/10.1021/ma900279a
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N-heterocyclic carbene-induced zwitterionic ring-opening polymerization of ethylene oxide and direct synthesis of α,ω-difunctionalized poly(ethylene oxide)s and poly(ethylene oxide)-b-poly(ε-caprolactone) block copolymers. In Journal of the American Chemical Society (Vol. 131, Issue 9, p. 3201-3209). https://doi.org/10.1021/ja809246f
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Dynamic accumulation of 4-desmethylsterols and phytostanols during ripening of Tunisian Meski olives (Olea europea L.). In Food Chemistry (Vol. 112, Issue 4, p. 897-902). https://doi.org/10.1016/j.foodchem.2008.06.068
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α-Tocopherol and fatty acids contents of some Tunisian table olives (Olea europea L.): Changes in their composition during ripening and processing. In Food Chemistry (Vol. 108, Issue 3, p. 833-839). https://doi.org/10.1016/j.foodchem.2007.11.043
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Structural diversity of nucleophilic adducts from flavanols and oak wood aldehydes. In Food Chemistry (Vol. 107, Issue 4, p. 1494-1505). https://doi.org/10.1016/j.foodchem.2007.10.012
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Pyrolysis-gas chromatography/mass spectrometry of Quercus sp. wood: Application to structural elucidation of macromolecules and aromatic profiles of different species. In Journal of Analytical and Applied Pyrolysis (Vol. 75, Issue 2, p. 181-193). https://doi.org/10.1016/j.jaap.2005.05.006
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8-O-Azeloyl-14-benzoylaconine: A new alkaloid from the roots of Aconitum karacolicum Rapcs and its antiproliferative activities. In Bioorganic and Medicinal Chemistry (Vol. 13, Issue 23, p. 6493-6501). https://doi.org/10.1016/j.bmc.2005.07.015
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Global fractionation of oak heartwood extractable polymers (lignins, polysaccharides and ellagitannins) by selective precipitations. In Journal of the Science of Food and Agriculture (Vol. 85, Issue 3, p. 343-353). https://doi.org/10.1002/jsfa.1991
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Differentiation of proanthocyanidin tannins from seeds, skins and stems of grapes (Vitis vinifera) and heartwood of Quebracho (Schinopsis balansae) by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and thioacidolysis/liquid chromatography/electrospray ionization mass spectrometry. In Analytica Chimica Acta (Vol. 513, Issue 1, p. 247-256). https://doi.org/10.1016/j.aca.2003.11.085
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Application of off-line size-exclusion chromatographic fractionation- matrix assisted laser desorption ionization time of flight mass spectrometry for proanthocyanidin characterization. In Journal of Chromatography A (Vol. 1033, Issue 2, p. 291-297). https://doi.org/10.1016/j.chroma.2004.01.052
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Facile Synthesis of a Fullerene-Barbituric Acid Derivative and Supramolecular Catalysis of Its Photoinduced Dimerization. In Journal of the American Chemical Society (Vol. 125, Issue 43, p. 13004-13005). https://doi.org/10.1021/ja0372098
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Study and quantification of monomeric flavan-3-ol and dimeric procyanidin quinonic forms by HPLC/ESI-MS. Application to red wine oxidation. In Journal of the Science of Food and Agriculture (Vol. 81, Issue 12, p. 1172-1179). https://doi.org/10.1002/jsfa.926
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