J. R. Maisin, C. Albert, A. Henry, J. Song, S. Han et al., Reduction of Short-Term Radiation Lethality by Biological Response Modifiers Given Alone or in Association with Other Chemical Protectors, Radiation Research, vol.135, issue.3, pp.332-337, 1993.
DOI : 10.2307/3578872

S. J. Hosseinimehr, V. Zakaryaee, and M. Froughizadeh, Oral oxymetholone reduces mortality induced by gamma irradiation in mice through stimulation of hematopoietic cells, Molecular and Cellular Biochemistry, vol.485, issue.1-2, pp.193-199, 2006.
DOI : 10.1007/s11010-005-9111-5

I. Stickney, D. R. Dowding, C. Authier, S. Garsd, A. Onizuka-handa et al., 5-androstenediol stimulates multilineage hematopoiesis in rhesus monkeys with radiation-induced myelosuppression, International Immunopharmacology, vol.6, issue.11, pp.1706-1713, 2006.
DOI : 10.1016/j.intimp.2006.07.005

L. G. Burdelya, V. I. Krivokrysenko, T. C. Tallant, E. Strom, A. S. Gleiberman et al., An Agonist of Toll-Like Receptor 5 Has Radioprotective Activity in Mouse and Primate Models, Science, vol.320, issue.5873, pp.226-230, 2008.
DOI : 10.1126/science.1154986

C. S. Potten, A. V. Gudkov, and E. A. Komarova, The significance of spontaneous and induced apoptosis in the gastrointestinal tract of mice, Cancer and Metastasis Review, vol.53, issue.2, pp.179-195, 1992.
DOI : 10.1007/BF00048063

R. Kolesnick and Z. Fuks, Radiation and ceramide-induced apoptosis, Oncogene, vol.22, issue.37, pp.5897-5906, 2003.
DOI : 10.1038/sj.onc.1206702

URL : http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.467.3998

G. Rima, J. Satgé, R. Dagiral, C. Lion, M. Fatôme et al., Synthesis and application of new organometallic compounds of silicon and germanium in chemical radioprotection, Applied Organometallic Chemistry, vol.5, issue.8, pp.583-594, 1999.
DOI : 10.1002/(SICI)1099-0739(199908)13:8<583::AID-AOC892>3.0.CO;2-D

R. Brückner, The Synthesis of gama-Alkylidenebutenolides, Current Organic Chemistry, vol.5, issue.6, pp.679-718, 2001.
DOI : 10.2174/1385272013375300

F. R. Foden, J. Mccormick, J. O-'mant, and D. M. , Vulpinic acids as potential antiinflammatory agents. 1. Vulpinic acids with substituents in the aromatic rings, Journal of Medicinal Chemistry, vol.18, issue.2, pp.199-203, 1975.
DOI : 10.1021/jm00236a020

D. Habrant, L. Roux, A. Poigny, S. Meunier, S. Wagner et al., Synthesis of Pulvinic Derivatives via TBAF-Mediated Regioselective Opening of an Unsymmetrical Monoaromatic Pulvinic Dilactone, The Journal of Organic Chemistry, vol.73, issue.23, pp.9490-9493, 2008.
DOI : 10.1021/jo801817s

H. W. Moore, R. J. Wikholm, R. J. Wikholm, H. W. Moore, H. Lohrisch et al., Perkin Trans, Tetrahedron Lett. J. Am. Chem. Soc. Justus Liebigs Ann. Chem. Tetrahedron Lett. J. Chem. Soc, vol.9, issue.1, pp.5049-5052, 1968.

. Un-mélange-d, 14 mmol, 1 éq éq.), d'hydroxyde de potassium (1,84 g éq.) et d'iodure de sodium (40 mg, 263 µmol, 2 mol %) dans EtOH (60 mL) est chauffé à reflux pendant 22 h. La réaction est laissée refroidir à t.a. puis une solution aqueuse de HCl 3N (60 mL) est ajoutée. Le précipité formé est filtré, p.55

K. Ogura, Y. Ito, and G. B. Tsughihashi, A New Synthesis of Arylacetic Esters Starting from Aromatic Aldehyde by the Use of Methyl (Methylthio)methyl Sulfoxide, Bulletin of the Chemical Society of Japan, vol.52, issue.7, pp.2013-2022, 1979.
DOI : 10.1246/bcsj.52.2013

. Hz, 83 (s, 3H

. Selon-la-procédure-représentative-d, estérification décrite pour 179a, l'acide 4-méthoxyphénylacétique (3,6 g, 21,6 mmol, 1,2 éq.) et l'alcool 176c (3,78 g, 18,0 mmol, 1 éq.) conduisent à l'éther 179b

G. V. Buxton, L. In, M. Mostafavi, M. Douki, T. Belloni et al., Radiation chemistry, from basics to applications in material and life sciences, pp.3-16, 2008.

J. Nénot, Effets biologiques des rayonnements ionisants, Techniques de l'ingénieur, BN3902, 1999.

L. Lee, N. Koo, and D. B. Min, Reactive Oxygen Species, Aging, and Antioxidative Nutraceuticals, Comprehensive Reviews in Food Science and Food Safety, vol.72, issue.2, pp.21-33, 2004.
DOI : 10.1016/S0891-5849(99)00047-7

L. Bravo, Polyphenols: Chemistry, Dietary Sources, Metabolism, and Nutritional Significance, Nutrition Reviews, vol.56, issue.11, pp.317-333, 1998.
DOI : 10.1111/j.1753-4887.1998.tb01670.x

URL : https://digital.csic.es/bitstream/10261/88474/1/accesoRestringido.pdf

S. J. Hosseinimehr, Drug Discovery Today, pp.794-805, 2007.

H. M. Patt, E. B. Tyree, R. L. Straube, and D. E. Smith, Cysteine Protection against X Irradiation, Science, vol.110, issue.2852, pp.213-214, 1949.
DOI : 10.1126/science.110.2852.213

J. M. Yuhas, J. B. Storer, and . Nat, Cancer Inst, Yuhas J. M. Radiat. Res. Radiat. Res, vol.42, issue.54, pp.331-335, 1969.

R. F. Martin, S. Broadhurst, M. E. Reum, C. J. Squire, G. R. Clark et al., In Vitro Studies with Methylproamine: A Potent New Radioprotector, Cancer Research, vol.64, issue.3, pp.1067-1070, 2004.
DOI : 10.1158/0008-5472.CAN-03-2423

URL : https://hal.archives-ouvertes.fr/hal-00088421

O. Vajragupta, P. Boonchoong, Y. Sumanont, H. Watanabe, Y. Wongkrajang et al., Manganese-Based complexes of radical scavengers as neuroprotective agents, Bioorganic & Medicinal Chemistry, vol.11, issue.10, pp.2329-2337, 2003.
DOI : 10.1016/S0968-0896(03)00070-1

S. Emami, S. J. Hosseinimehr, S. M. Taghdisi, and S. Akhlaghpoor, Kojic acid and its manganese and zinc complexes as potential radioprotective agents, Bioorganic & Medicinal Chemistry Letters, vol.17, issue.1, pp.45-48, 2007.
DOI : 10.1016/j.bmcl.2006.09.097

F. Legué, N. Guitton, V. Brouazin-jousseaume, S. Colleu-durel, K. Nourgalieva et al., IL-6 A KEY CYTOKINE IN IN VITRO AND IN VIVO RESPONSE OF SERTOLI CELLS TO EXTERNAL GAMMA IRRADIATION, Cytokine, vol.16, issue.6, pp.232-238, 2001.
DOI : 10.1006/cyto.2001.0970

P. R. Streeter, L. Z. Dudley, and W. H. Fleming, Activation of the G-CSF and Flt-3 receptors protects hematopoietic stem cells from lethal irradiation, Experimental Hematology, vol.31, issue.11, pp.1119-1123, 2003.
DOI : 10.1016/S0301-472X(03)00257-1

J. R. Maisin, C. Albert, A. Henry, J. Song, S. Han et al., Reduction of Short-Term Radiation Lethality by Biological Response Modifiers Given Alone or in Association with Other Chemical Protectors, Radiation Research, vol.135, issue.3, pp.332-337, 1993.
DOI : 10.2307/3578872

S. J. Hosseinimehr, V. Zakaryaee, and M. Froughizadeh, Oral oxymetholone reduces mortality induced by gamma irradiation in mice through stimulation of hematopoietic cells, Molecular and Cellular Biochemistry, vol.485, issue.1-2, pp.193-199, 2006.
DOI : 10.1007/s11010-005-9111-5

L. G. Burdelya, V. I. Krivokrysenko, T. C. Tallant, E. Strom, A. S. Gleiberman et al., An Agonist of Toll-Like Receptor 5 Has Radioprotective Activity in Mouse and Primate Models, Science, vol.320, issue.5873, pp.226-230, 2008.
DOI : 10.1126/science.1154986

C. S. Potten, A. V. Gudkov, E. A. Komarova, R. Kolesnick, and Z. Fuks, The significance of spontaneous and induced apoptosis in the gastrointestinal tract of mice, Cancer and Metastasis Review, vol.53, issue.2, pp.179-195, 1992.
DOI : 10.1007/BF00048063

G. Rima, J. Satgé, R. Dagiral, C. Lion, M. Fatôme et al., Synthesis and application of new organometallic compounds of silicon and germanium in chemical radioprotection, Applied Organometallic Chemistry, vol.5, issue.8, pp.583-594, 1999.
DOI : 10.1002/(SICI)1099-0739(199908)13:8<583::AID-AOC892>3.0.CO;2-D

J. F. Weiss and M. R. Landauer, Radioprotection by Antioxidantsa, Annals of the New York Academy of Sciences, vol.34, issue.Suppl. 6, pp.44-60, 2000.
DOI : 10.1111/j.1749-6632.2000.tb06175.x

S. R. Venkatachalam and S. Chattopadhyay, Natural Radioprotective Agents: An Overview, Current Organic Chemistry, vol.9, issue.4, pp.389-404, 2005.
DOI : 10.2174/1385272053174930

B. Steffan and W. Steglich, Pigments from the Cap Cuticle of the Bay Boletus (Xerocomus badius), Angewandte Chemie International Edition in English, vol.1968, issue.6, pp.445-447, 1984.
DOI : 10.1002/anie.198404451

M. Winner, A. Gimenez, H. Schmidt, B. Sontag, B. Steffan et al., Unusual Pulvinic Acid Dimers from the Common FungiScleroderma citrinum (Common Earthball) andChalciporus piperatus (Peppery Bolete), Angewandte Chemie International Edition, vol.43, issue.14, pp.1883-1886, 2004.
DOI : 10.1002/anie.200352529

K. Mosbach, Biosynthesis of Lichen Substances, Products of a Symbiotic Association, Angewandte Chemie International Edition in English, vol.8, issue.4, pp.240-250, 1969.
DOI : 10.1002/anie.196902401

R. Brückner, The Synthesis of gama-Alkylidenebutenolides, Current Organic Chemistry, vol.5, issue.6, pp.679-718, 2001.
DOI : 10.2174/1385272013375300

B. Åkermark, Studies on the Chemistry of Lichens. 14. The Structure of Calycin., Acta Chemica Scandinavica, vol.15, pp.1695-1700, 1961.
DOI : 10.3891/acta.chem.scand.15-1695

F. R. Foden, J. Mccormick, J. O-'mant, and D. M. , Vulpinic acids as potential antiinflammatory agents. 1. Vulpinic acids with substituents in the aromatic rings, Journal of Medicinal Chemistry, vol.18, issue.2, pp.199-203, 1975.
DOI : 10.1021/jm00236a020

D. Habrant, L. Roux, A. Poigny, S. Meunier, S. Wagner et al., Synthesis of Pulvinic Derivatives via TBAF-Mediated Regioselective Opening of an Unsymmetrical Monoaromatic Pulvinic Dilactone, The Journal of Organic Chemistry, vol.73, issue.23, pp.9490-9493, 2008.
DOI : 10.1021/jo801817s

H. W. Moore, H. R. Shelden, D. W. Deters, and R. J. Wikholm, Rearrangements of azidoquinones. V. Stereoselective acid-catalyzed rearrangements of azidoquinones to .gamma.-cyanoalkylidine- (cyanoarylidine-) .DELTA..alpha.,.beta.-butenolides, Journal of the American Chemical Society, vol.92, issue.6, pp.1675-1681, 1970.
DOI : 10.1021/ja00709a043

G. Pattenden, N. Pegg, and A. G. Smith, A new synthesis of pulvinic acids., Tetrahedron Letters, vol.27, issue.3, pp.403-406, 1986.
DOI : 10.1016/S0040-4039(00)84030-7

J. Weinstock, J. E. Blank, H. Oh, and B. M. Sutton, Regiospecific synthesis of substituted vulpinic acids, The Journal of Organic Chemistry, vol.44, issue.5, pp.673-676, 1979.
DOI : 10.1021/jo01319a002

P. Langer, M. Stoll, P. Langer, T. Schneider, and M. Stoll, Regio- and Stereoselective Synthesis of??-Alkylidenebutenolides by Cyclization of Dilithiated 1,3-Dicarbonyl Compounds withN,N???-Dimethoxy-N,N???-dimethylethane- diamide, Angewandte Chemie International Edition, vol.38, issue.12, pp.1803-1805, 1999.
DOI : 10.1002/(SICI)1521-3773(19990614)38:12<1803::AID-ANIE1803>3.0.CO;2-5

P. Langer, T. Eckardt, T. Schneider, C. Gobel, and R. Herbst-irmer, Efficient Synthesis of ??-Alkylidenetetronic Esters by Sequential Lewis Acid Catalyzed [3 + 2] Cyclizations and Palladium-Catalyzed Cross-Coupling Reactions, The Journal of Organic Chemistry, vol.66, issue.7, pp.2222-2226, 2001.
DOI : 10.1021/jo005565s

Z. Ahmed and P. Langer, Suzuki Cross-Coupling Reactions of ??-Alkylidenebutenolides:?? Application to the Synthesis of Vulpinic Acid, The Journal of Organic Chemistry, vol.69, issue.11, pp.3753-3757, 2004.
DOI : 10.1021/jo049780a

Z. Ahmed, P. Langer, Z. Ahmed, U. Albrecht, and P. Langer, Synthesis of natural pulvinic acids based on a ???[3+2] cyclization???Suzuki cross-coupling??? strategy, Tetrahedron, vol.61, issue.8, pp.2055-2063, 2005.
DOI : 10.1016/j.tet.2004.12.048

M. Desage-el-murr, S. Nowaczyk, L. Gall, T. Mioskowski, C. Amekraz et al., Norbadione A: Synthetic Approach to the Bis(pulvinic acid) Moiety and Cesium-Complexation Studies, Angewandte Chemie International Edition, vol.42, issue.11, pp.1289-1293, 2003.
DOI : 10.1002/anie.200390332

B. Heurtaux, C. Lion, L. Gall, T. Mioskowski, and C. , Uncatalyzed Reaction of Silyl Ketene Acetals with Oxalyl Chloride:?? A Straightforward Preparation of Symmetrical Pulvinic Acids, The Journal of Organic Chemistry, vol.70, issue.4, pp.1474-1477, 2005.
DOI : 10.1021/jo048403v

C. Willis, E. Bodio, Y. Bourdreux, C. Billaud, L. Gall et al., Flexible synthesis of vulpinic acids from tetronic acid, Tetrahedron Letters, vol.48, issue.37, pp.6421-6424, 2007.
DOI : 10.1016/j.tetlet.2007.07.094

A. Mallinger, L. Gall, T. Mioskowski, and C. , 3-Aryltetronic Acids: Efficient Preparation and Use as Precursors for Vulpinic Acids, The Journal of Organic Chemistry, vol.74, issue.3, pp.1124-1129, 2009.
DOI : 10.1021/jo802038z

U. Söderberg, Note on the Action of Vulpinic Acid., Acta Physiologica Scandinavica, vol.5, issue.2-3, pp.97-98, 1953.
DOI : 10.1111/j.1748-1716.1953.tb00927.x

B. B. Newbould and . Brit, CHEMOTHERAPY OF ARTHRITIS INDUCED IN RATS BY MYCOBACTERIAL ADJUVANT, British Journal of Pharmacology and Chemotherapy, vol.111, issue.1, pp.127-136, 1963.
DOI : 10.1111/j.1476-5381.1963.tb01508.x

R. G. Benedict and L. R. Brady, Antimicrobial Activity of Mushroom Metabolites, Journal of Pharmaceutical Sciences, vol.61, issue.11, pp.1820-1822, 1972.
DOI : 10.1002/jps.2600611130

S. A. Van-der-sar, J. W. Blunt, A. L. Cole, L. B. Din, and M. H. Munro, sp., Journal of Natural Products, vol.68, issue.12, pp.1799-1801, 2005.
DOI : 10.1021/np0503395

D. Dias, J. M. White, and S. Urban, Pinastric acid revisited: a complete NMR and X-ray structure assignment, Natural Product Research, vol.41, issue.4, pp.366-376, 2007.
DOI : 10.1107/S0021889899006020

L. J. Rashan, M. T. Ayoub, L. Al-omar, and R. W. Al-khayatt, Vulpinic acids inhibit influenza (RNA) viruses but not herpes (DNA) viruses, World Journal of Microbiology & Biotechnology, vol.41, issue.2, pp.155-158, 1990.
DOI : 10.1007/BF01200935

A. Kasuga, Y. Aoyagi, and T. Sugahara, Antioxidant Activity of Fungus Suihs bovinus (L: Fr.) O. Kuntze, Journal of Food Science, vol.29, issue.8, pp.1113-1115, 1995.
DOI : 10.1111/j.1365-2621.1995.tb06304.x

S. Meunier, M. Desage-el-murr, S. Nowaczyk, L. Gall, T. Pin et al., A Powerful Antiradiation Compound Revealed by a New High-Throughput Screening Method, ChemBioChem, vol.57, issue.6, pp.832-840, 2004.
DOI : 10.1002/cbic.200300787

D. Habrant, S. Poigny, M. Ségur-derai, Y. Brunel, B. Heurtaux et al., Evaluation of Antioxidant Properties of Monoaromatic Derivatives of Pulvinic Acids, Journal of Medicinal Chemistry, vol.52, issue.8, pp.2454-2464, 2009.
DOI : 10.1021/jm801500h

M. Gill, M. J. Kiefel, D. A. Lally, and A. Ten, Pigments of Fungi. XV. An Efficient, Unambiguous Route to Unsymmetrically Substituted Dibenzyl Acyloins and Their Use in the Synthesis of Fungus Pigments of the Pulvinone and Grevillin Types, Australian Journal of Chemistry, vol.43, issue.9, pp.1497-1518, 1990.
DOI : 10.1071/CH9901497

S. Brandänge, L. Flodman, and A. Norberg, Studies on the intramolecular Claisen condensation: facile synthesis of tetronic acids, The Journal of Organic Chemistry, vol.49, issue.5, pp.927-928, 1984.
DOI : 10.1021/jo00179a034

J. Wang and B. L. Pagenkopf, First Total Synthesis and Structural Reassignment of (???)-Aplysiallene, Organic Letters, vol.9, issue.18, pp.3703-3706, 2007.
DOI : 10.1021/ol701797e

G. Brogginia, L. Garantib, G. Moltenib, and G. Zecchia, The first case of asymmetric induction in intramolecular nitrile imine cycloadditions: synthesis of enantiopure 3-substituted 6-oxo-2,3,3a,5-tetrahydro-4-carbomethoxy-furo[3,4-c]pyrazoles, Tetrahedron: Asymmetry, vol.10, issue.3, pp.487-492, 1999.
DOI : 10.1016/S0957-4166(99)00012-9

B. Nadal, P. Thuéry, L. Gall, and T. , Synthesis of vulpinic acids from dimethyl tartrate, Tetrahedron Letters, vol.50, issue.20, pp.2430-2433, 2009.
DOI : 10.1016/j.tetlet.2009.03.011

M. Adinolfi, M. Parrilli, G. Barone, G. Laonigro, L. Mangoni et al., A: Chem, Tetrahedron Lett. J. Chem. Soc., Perkin Trans. Synlett, vol.17, issue.267, pp.3661-3662, 1976.

E. G. Occhiato, A. Trabocchi, and A. Guarna, -Alkoxycarbonyl Lactams with Boronic Acids and Esters, The Journal of Organic Chemistry, vol.66, issue.7, pp.2459-2465, 2001.
DOI : 10.1021/jo001807c

N. Ojima, S. Takenaka, and S. Seto, New butenolides from Aspergillus terreus, Phytochemistry, vol.12, issue.10, pp.2527-2529, 1973.
DOI : 10.1016/0031-9422(73)80469-8

K. Rehse and J. Lehmke, Anticoagulante 3-Aryl-5-benzylidentetrons??uren, Archiv der Pharmazie, vol.317, issue.1, pp.11-14, 1985.
DOI : 10.1002/ardp.19853180104

S. Antane, C. E. Caufield, W. Hu, D. Keeney, P. Labthavikul et al., Pulvinones as bacterial cell wall biosynthesis inhibitors, Bioorganic & Medicinal Chemistry Letters, vol.16, issue.1, pp.176-180, 2006.
DOI : 10.1016/j.bmcl.2005.09.021

L. Claisen and T. Ewan, Ueber die Einwirkung des Oxal??thers auf Dibenzylketon, Justus Liebig's Annalen der Chemie, vol.219, issue.3, pp.245-299
DOI : 10.1002/jlac.18952840302

G. A. Kraus and K. Landgrebe, Stannyl ester cyclizations, Tetrahedron, vol.41, issue.19, pp.4039-4046, 1985.
DOI : 10.1016/S0040-4020(01)97182-0

T. W. Greene and P. G. Wuts, Protective Groups In Organic Synthesis, pp.67-72, 1991.
DOI : 10.1002/0471220574

A. Li and F. Kong, Concise syntheses of arabinogalactans with ??-(1???6)-linked galactopyranose backbones and ??-(1???3)- and ??-(1???2)-linked arabinofuranose side chains, Bioorganic & Medicinal Chemistry, vol.13, issue.3, pp.839-853, 2005.
DOI : 10.1016/j.bmc.2004.10.035

R. Schobert and A. Schlenk, Tetramic and tetronic acids: An update on new derivatives and biological aspects, Bioorganic & Medicinal Chemistry, vol.16, issue.8, pp.4203-4221, 2008.
DOI : 10.1016/j.bmc.2008.02.069

T. Rosset, R. H. Sankhala, C. E. Stickings, M. E. Taylor, and R. Thomas, Auct.: culture filtrate products, Biochemical Journal, vol.67, issue.3, pp.390-400, 1957.
DOI : 10.1042/bj0670390

C. W. Holzapfel, The isolation and structure of cyclopiazonic acid, a toxic metabolite of penicillium cyclopium westling, Tetrahedron, vol.24, issue.5, pp.2101-2119, 1968.
DOI : 10.1016/0040-4020(68)88113-X

M. Ito, H. Okui, H. Nakagawa, S. Mio, A. Kinoshita et al., -Oxydihydropyrroles: 4-Hydroxy-3-mesityl-5,5-dimethyl Derivatives with Various Substituents at the 1-Position, Bioscience, Biotechnology, and Biochemistry, vol.66, issue.11, pp.2406-2414, 2002.
DOI : 10.1271/bbb.66.2406

URL : https://hal.archives-ouvertes.fr/jpa-00209846

M. Ito, H. Okui, H. Nakagawa, S. Mio, A. Kinoshita et al., Synthesis and insecticidal activity of novel N-oxydihydropyrroles: 4-hydroxy-3-mesityl-1-methoxymethoxy derivatives with various substituents at the 5-position, Bioorganic & Medicinal Chemistry, vol.11, issue.5, pp.761-768, 2003.
DOI : 10.1016/S0968-0896(02)00474-1

S. Gabriel and . Ber, Zur Kenntnis der Tetrams??uren, Berichte der deutschen chemischen Gesellschaft, vol.46, issue.3, pp.3033-3039, 1914.
DOI : 10.1002/cber.191404703102

H. Hening and A. Gelbin, Advances in Tetramic Acid Chemistry, Adv. Heterocycl. Chem, vol.57, pp.139-185, 1993.
DOI : 10.1016/S0065-2725(08)60888-0

J. A. King and F. H. Mcmillan, The Preparation of Some ??-Benzylamino-??,??-dialkoxypropionic Acid Derivatives, Journal of the American Chemical Society, vol.72, issue.3, pp.1236-1240, 1950.
DOI : 10.1021/ja01159a047

M. Storgaard, F. Z. Dörwald, B. Peschke, and D. Tanner, Palladium-Catalyzed ??-Arylation of Tetramic Acids, The Journal of Organic Chemistry, vol.74, issue.14, pp.5032-5040, 2009.
DOI : 10.1021/jo900799y

S. R. Baker, A. F. Parsons, and M. Wilson, A radical approach to debenzylation of amides, Tetrahedron Letters, vol.39, issue.3-4, pp.331-332, 1998.
DOI : 10.1016/S0040-4039(97)10480-4

R. H. Schlessinger and G. R. Bebernitz, A versatile 3-acyltetramic acid reagent, The Journal of Organic Chemistry, vol.50, issue.8, pp.1344-1346, 1985.
DOI : 10.1021/jo00208a053

L. M. Magalhães, M. A. Segundo, S. Reis, and J. L. Lima, Methodological aspects about in vitro evaluation of antioxidant properties, Analytica Chimica Acta, vol.613, issue.1, pp.1-19, 2008.
DOI : 10.1016/j.aca.2008.02.047

G. H. Cao, H. M. Alessio, and R. G. Cutler, Oxygen-radical absorbance capacity assay for antioxidants, Free Radical Biology and Medicine, vol.14, issue.3, pp.303-311, 1993.
DOI : 10.1016/0891-5849(93)90027-R

G. Cao and R. L. Prior, [5]Measurement of oxygen radical absorbance capacity in biological samples, Methods Enzymol, vol.299, pp.50-62, 1999.
DOI : 10.1016/S0076-6879(99)99008-0

B. Ou, M. Hampsch-woodill, and R. L. Prior, Development and Validation of an Improved Oxygen Radical Absorbance Capacity Assay Using Fluorescein as the Fluorescent Probe, Journal of Agricultural and Food Chemistry, vol.49, issue.10, pp.4619-4626, 2001.
DOI : 10.1021/jf010586o

G. W. Winston, F. Regoli, A. J. Dugas, . Jr, J. H. Fong et al., A Rapid Gas Chromatographic Assay for Determining Oxyradical Scavenging Capacity of Antioxidants and Biological Fluids, Free Radical Biology and Medicine, vol.24, issue.3, pp.480-493, 1998.
DOI : 10.1016/S0891-5849(97)00277-3

I. F. Benzie and J. J. Strain, The Ferric Reducing Ability of Plasma (FRAP) as a Measure of ???Antioxidant Power???: The FRAP Assay, Analytical Biochemistry, vol.239, issue.1, pp.70-76, 1996.
DOI : 10.1006/abio.1996.0292

R. Apak, K. G. Güçlü, M. Özyürek, and S. E. Karademir, Novel Total Antioxidant Capacity Index for Dietary Polyphenols and Vitamins C and E, Using Their Cupric Ion Reducing Capability in the Presence of Neocuproine:?? CUPRAC Method, Journal of Agricultural and Food Chemistry, vol.52, issue.26, pp.7970-7981, 2004.
DOI : 10.1021/jf048741x

Z. Du and W. J. Bramlage, Modified thiobarbituric acid assay for measuring lipid oxidation in sugar-rich plant tissue extracts, Journal of Agricultural and Food Chemistry, vol.40, issue.9, pp.1566-1570, 1992.
DOI : 10.1021/jf00021a018

B. Salles, C. Provost, P. Calsou, I. Hennebelle, I. Gosset et al., A Chemiluminescent Microplate Assay to Detect DNA Damage Induced by Genotoxic Treatments, Analytical Biochemistry, vol.232, issue.1, pp.37-42, 1995.
DOI : 10.1006/abio.1995.9964

G. L. Ellman, K. D. Courtney, V. Andres, and R. M. Featherstone, A new and rapid colorimetric determination of acetylcholinesterase activity, Biochemical Pharmacology, vol.7, issue.2, pp.88-95, 1961.
DOI : 10.1016/0006-2952(61)90145-9

C. Henriquez, C. Aliaga, and E. Lissi, Formation and decay of the ABTS derived radical cation: A comparison of different preparation procedures, International Journal of Chemical Kinetics, vol.379, issue.12, pp.659-665, 2002.
DOI : 10.1002/kin.10094

C. Privat, J. P. Telo, V. Bernardes-genisson, A. Vieira, J. Souchard et al., -??-Viniferin As Compared to Stilbene Derivatives in Aqueous and Nonaqueous Media, Journal of Agricultural and Food Chemistry, vol.50, issue.5, pp.1213-1217, 2002.
DOI : 10.1021/jf010676t

O. 'brien, J. Wilson, I. Orton, T. Pognan, and F. , Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity, European Journal of Biochemistry, vol.107, issue.17, pp.5421-5426, 2000.
DOI : 10.1046/j.1432-1327.2000.01606.x

K. Ogura, Y. Ito, and G. B. Tsughihashi, A New Synthesis of Arylacetic Esters Starting from Aromatic Aldehyde by the Use of Methyl (Methylthio)methyl Sulfoxide, Bulletin of the Chemical Society of Japan, vol.52, issue.7, pp.2013-2022, 1979.
DOI : 10.1246/bcsj.52.2013

M. Costa, E. Dalcanale, S. Dias, F. Graiff, C. Tiripicchio et al., New trisubstituted cyclopentadienyl ligands: synthesis, characterisation and catalytic properties of mono and dinuclear cobalt, rhodium, iron and ruthenium complexes, Journal of Organometallic Chemistry, vol.619, issue.1-2, pp.179-193, 2001.
DOI : 10.1016/S0022-328X(00)00652-5

B. J. Bradbury, J. Baumgold, R. Paek, U. Kammula, J. Zimmet et al., Muscarinic receptor binding and activation of second messengers by substituted N-methyl-N-[4-(1-azacycloalkyl)-2-butynyl]acetamides, Journal of Medicinal Chemistry, vol.34, issue.3, pp.1073-1079, 1991.
DOI : 10.1021/jm00107a029

L. C. Meurer, R. L. Tolman, E. W. Chapin, R. Saperstein, P. P. Vicario et al., Synthesis and hypoglycemic activity of substituted 8-(1-piperazinyl)imidazo[1,2-a]pyrazines, Journal of Medicinal Chemistry, vol.35, issue.21, pp.3845-3857, 1992.
DOI : 10.1021/jm00099a012