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Téléphone
05 40 00 62 85
Groupe de recherche
Catalysis, Synthesis and Health
Statut
Permanent
Poste
Enseignant-chercheur
Batiment
A12
Etage
1° Ouest
Parcours
2004-Présent : Maître de conférences, Université Bordeaux 1, Pr. E. Fouquet
2003-2004 : A.T.E.R, Université Bordeaux 1, Pr. D. Astruc
2001-2002 : Stage post-doctoral, Université Montpellier 2, Dr. F. Lamaty
2000-2001 : Stage post-doctoral, Harvard University (USA), Pr. Y. Kishi
1996-1999 : Doctorat de l’Université Paris XI, avec Label Européen (Mention très honorable), Faculté de Pharmacie de Châtenay Malabry, Université Paris-Sud 11, (Dr. B Figadère
1997 : Diplôme d’état de Docteur en Pharmacie (Mention très honorable), Université Paris-Sud 11
Contact
magali.szlosek@u-bordeaux.fr
ISM, UMR-CNRS 5255, Groupe CSH Université de Bordeaux, Bât. A12
351, cours de la libération 33405 TALENCE Cedex
Publications
From the gold-catalysed benzylation of arenes to the regio- and stereoselective synthesis of procyanidins dimers. In Tetrahedron (Vol. 71, Issue 20, p. 3045-3051). https://doi.org/10.1016/j.tet.2014.11.011
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How wine polyphenols can fight Alzheimer disease progression: Towards a molecular explanation. In Tetrahedron (Vol. 71, Issue 20, p. 3163-3170). https://doi.org/10.1016/j.tet.2014.06.091
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A new sif-dipropargyl glycerol scaffold as a versatile prosthetic group to design dimeric radioligands: Synthesis of the [18f]bmppsif tracer to image serotonin receptors. In ChemMedChem (Vol. 9, Issue 2, p. 337-349). https://doi.org/10.1002/cmdc.201300458
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Pd0-catalyzed methyl transfer on nucleosides and oligonucleotides, envisaged as a PET tracer. In Molecules (Vol. 18, Issue 11, p. 13654-13665). https://doi.org/10.3390/molecules181113654
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11C click chemistry using [11C]methyl azide: Simplified, versatile, and practical alternative access to [11C] Nucleosides and [11C]oligonucleotides for PET imaging. In European Journal of Organic Chemistry (Issue 7, p. 1214-1217). https://doi.org/10.1002/ejoc.201201379
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[ 18F]Si-RiboRGD: From design and synthesis to the imaging of α v β 3 integrins in melanoma tumors. In ChemPlusChem (Vol. 77, Issue 5, p. 345-349). https://doi.org/10.1002/cplu.201200022
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Polyphenols and alzheimer’s disease: Tau/polyphenol interactions investigated by NMR and molecular modelling. In Nutrition and Aging (Vol. 1, Issue 3-4, p. 201-206). https://doi.org/10.3233/NUA-130015
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Silicon-based chemistry: An original and efficient one-step approach to [18F]-Nucleosides and [18F]-Oligonucleotides for PET imaging. In Chemistry - A European Journal (Vol. 17, Issue 11, p. 3096-3100). https://doi.org/10.1002/chem.201003234
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A 'click chemistry' approach to the efficient synthesis of modified nucleosides and oligonucleotides for PET imaging. In Tetrahedron Letters (Vol. 51, Issue 8, p. 1230-1232). https://doi.org/10.1016/j.tetlet.2009.12.120
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State of art in 11C labelled radiotracers synthesis. In Current Medicinal Chemistry (Vol. 15, Issue 3, p. 235-277). https://doi.org/10.2174/092986708783497292
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Efficient synthetic approach to heterocycles possessing the 3,3-disubstituted-2,3-dihydrobenzofuran skeleton via diverse palladium-catalyzed tandem reactions. In Tetrahedron (Vol. 63, Issue 16, p. 3340-3349). https://doi.org/10.1016/j.tet.2007.02.035
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Palladium-catalyzed cascade allylation/carbopalladation/cross coupling: A novel three-component reaction for the synthesis of 3,3-disubstituted-2,3- dihydrobenzofurans. In Tetrahedron Letters (Vol. 44, Issue 48, p. 8657-8659). https://doi.org/10.1016/j.tetlet.2003.09.169
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Complete structure of the mycolactones [10]. In Journal of the American Chemical Society (Vol. 123, Issue 41, p. 10117-10118). https://doi.org/10.1021/ja011824z
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Highly enantioselective aldol reaction with 2-trimethylsilyloxyfuran: The first catalytic asymmetric autoinductive aldol reaction. In Angewandte Chemie - International Edition (Vol. 39, Issue 10, p. 1799-1801). https://doi.org/10.1002/(SICI)1521-3773(20000515)39:10<1799::AID-ANIE1799>3.0.CO;2-Z
().
Ligand effects on the catalytic asymmetric autoinductive aldol reaction of 2-TMSOF (2-trimethylsilyloxyfuran) with aldehydes. In Heterocycles (Vol. 52, Issue 3, p. 1005-1013). https://doi.org/10.3987/com-99-s103
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Acetogenins of annonaceae. Part 86: Synthesis of a highly functionalized precursor of (-)-4-deoxygigantecin, an annonaceous acetogenin. In New Journal of Chemistry (Vol. 24, Issue 5, p. 337-342). https://doi.org/10.1039/b000236o
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Highly Enantioselective 1,2-Addition of 2-[(Trimethylsilyl)oxy]furan to Aldehydes: Application to Muricatacin Synthesis. In Journal of Organic Chemistry (Vol. 63, Issue 15, p. 5169-5172). https://doi.org/10.1021/jo9804137
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Glaucabellin and glaucaflorin, two acetogenins from Annona glauca. In Phytochemistry (Vol. 48, Issue 1, p. 141-145). https://doi.org/10.1016/S0031-9422(97)01103-5
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Study of the structure-activity relationships of the acetogenin of annonaceae, muricatacin and analogues. In European Journal of Medicinal Chemistry (Vol. 32, Issue 7-8, p. 617-623). https://doi.org/10.1016/S0223-5234(97)83287-4
().