]. R. Crittenden and M. J. Playne, Production, properties and applications of food-grade oligosaccharides, Trends in Food Science & Technology, vol.7, issue.11, pp.353-361, 1996.
DOI : 10.1016/S0924-2244(96)10038-8

C. Grootaert, J. A. Delcour, C. M. Courtin, W. F. Broekaert, W. Verstraete et al., Microbial metabolism and prebiotic potency of arabinoxylan oligosaccharides in the human intestine, Trends in Food Science & Technology, vol.18, issue.2, pp.64-71, 2007.
DOI : 10.1016/j.tifs.2006.08.004

]. J. Yun, Fructooligosaccharides???Occurrence, preparation, and application, Enzyme and Microbial Technology, vol.19, issue.2, pp.107-117, 1996.
DOI : 10.1016/0141-0229(95)00188-3

]. W. Weis and K. Drickamer, Structural Basis of Lectin-Carbohydrate Recognition, Annual Review of Biochemistry, vol.65, issue.1, pp.441-473, 1996.
DOI : 10.1146/annurev.bi.65.070196.002301

]. L. Lasky, Selectins: interpreters of cell-specific carbohydrate information during inflammation, Science, vol.258, issue.5084, pp.964-969, 1992.
DOI : 10.1126/science.1439808

E. A. Merritt, S. Sarfaty, F. Van-den-akker, C. L. 'hoir, J. A. Martial et al., Crystal structure of cholera toxin B-pentamer bound to receptor GM1 pentasaccharide, Protein Science, vol.155, issue.2, pp.166-175, 1994.
DOI : 10.1016/S0070-2161(08)60539-0

J. M. Daubenspeck, H. Zeng, P. Chen, S. Dong, C. T. Steichen et al., Exosporium, Journal of Biological Chemistry, vol.230, issue.30, pp.30945-30953, 2004.
DOI : 10.1128/JB.186.2.566-569.2004

P. Anderson, M. E. Pichichero, and R. A. , Immunogens consisting of oligosaccharides from the capsule of Haemophilus influenzae type b coupled to diphtheria toxoid or the toxin protein CRM197., Journal of Clinical Investigation, vol.76, issue.1, pp.52-59, 1985.
DOI : 10.1172/JCI111976

L. Schofield, M. C. Hewitt, K. Evans, M. Siomos, and P. H. Seeberger, Synthetic GPI as a candidate anti-toxic vaccine in a model of malaria, Nature, vol.8, issue.6899, pp.785-789, 2002.
DOI : 10.1093/clinids/8.1.144

D. B. Werz and P. H. Seeberger, Carbohydrates as the Next Frontier in Pharmaceutical Research, Chemistry - A European Journal, vol.11, issue.11, pp.3194-3206, 2005.
DOI : 10.1007/978-1-4615-1267-7_28

D. H. Dube and C. R. Bertozzi, Glycans in cancer and inflammation ??? potential for therapeutics and diagnostics, Nature Reviews Drug Discovery, vol.22, issue.6, pp.477-488, 2005.
DOI : 10.1084/jem.182.4.1133

S. S. Pinho and C. A. Reis, Glycosylation in cancer: mechanisms and clinical implications, Nature Reviews Cancer, vol.16, issue.9, pp.540-555, 2015.
DOI : 10.1093/glycob/cwl034

S. J. Danishefsky, Y. Shue, M. N. Chang, and C. Wong, Development of Globo-H Cancer Vaccine, Accounts of Chemical Research, vol.48, issue.3, pp.643-652, 2015.
DOI : 10.1021/ar5004187

M. C. Bryan, F. Fazio, H. Lee, C. Huang, A. Chang et al., Covalent Display of Oligosaccharide Arrays in Microtiter Plates, Journal of the American Chemical Society, vol.126, issue.28, pp.8640-8641, 2004.
DOI : 10.1021/ja048433f

I. Matsumoto, H. Kitagaki, Y. Akai, Y. Ito, and N. Seno, Derivatization of epoxy-activated agarose with various carbohydrates for the preparation of stable and high-capacity affinity adsorbents: Their use for affinity chromatography of carbohydrate-binding proteins, Analytical Biochemistry, vol.116, issue.1, pp.103-110, 1981.
DOI : 10.1016/0003-2697(81)90329-8

M. Caron, R. Joubert-caron, J. R. Cartier, A. Chadli, and D. Bladier, Study of lectin???ganglioside interactions by high-performance liquid affinity chromatography, Journal of Chromatography A, vol.646, issue.2, pp.327-333, 1993.
DOI : 10.1016/0021-9673(93)83345-S

C. Orgeret, E. Seillier, C. Gautier, J. Defaye, and H. Driguez, 4-Thiocellooligosaccharides. Their synthesis and use as ligands for the separation of cellobiohydrolases of Trichoderma reesei by affinity chromatography, Carbohydrate Research, vol.224, pp.29-40, 1992.
DOI : 10.1016/0008-6215(92)84090-F
URL : https://hal.archives-ouvertes.fr/hal-00310371

I. Braccini and S. Pérez, -Induced Gelation in Alginates and Pectins:?? The Egg-Box Model Revisited, Biomacromolecules, vol.2, issue.4, pp.1089-1096, 2001.
DOI : 10.1021/bm010008g

K. Miyoshi, K. Uezu, K. Sakurai, and S. Shinkai, Proposal of a New Hydrogen-Bonding Form to Maintain Curdlan Triple Helix, Chemistry & Biodiversity, vol.1, issue.6, pp.916-924, 2004.
DOI : 10.1002/cbdv.200490073

K. Ferji, C. Nouvel, J. Babin, P. Albouy, M. Li et al., Controlled synthesis of new amphiphilic glycopolymers with liquid crystal grafts, Journal of Polymer Science Part A: Polymer Chemistry, vol.24, issue.18, pp.3829-3839, 2013.
DOI : 10.1002/marc.200300078
URL : https://hal.archives-ouvertes.fr/hal-01498209

U. G. Spizzirri, F. Iemma, G. Cirillo, I. Altimari, F. Puoci et al., Temperature-sensitive hydrogels by graft polymerization of chitosan and N-isopropylacrylamide for drug release, Pharmaceutical Development and Technology, vol.329, issue.5, pp.1026-1034, 2011.
DOI : 10.1016/j.ijpharm.2006.08.027

V. V. Braunmuehl, G. Jonas, and R. Stadler, Enzymic Grafting of Amylose from Poly(dimethylsiloxanes), Macromolecules, vol.28, issue.1, pp.17-24, 1995.
DOI : 10.1021/ma00105a003

A. Narumi, K. Kawasaki, H. Kaga, T. Satoh, N. Sugimoto et al., Glycoconjugated polymer 6. Synthesis of poly[styrene- block -(styrene- graft -amylose)] via potato phosphorylase-catalyzed polymerization, Polymer Bulletin, vol.49, issue.6, pp.405-410, 2003.
DOI : 10.1007/s00289-003-0126-3

Z. Tuzar and P. , Block and graft copolymer micelles in solution, Advances in Colloid and Interface Science, vol.6, issue.3, pp.201-232, 1976.
DOI : 10.1016/0001-8686(76)80009-7

T. Smart, H. Lomas, M. Massignani, M. V. Flores-merino, L. R. Perez et al., Block copolymer nanostructures, Nano Today, vol.3, issue.3-4, pp.38-46, 2008.
DOI : 10.1016/S1748-0132(08)70043-4

R. N. Goldberg, D. Bell, Y. B. Tewari, and M. A. Mclaughlin, Thermodynamics of hydrolysis of oligosaccharides, Biophysical Chemistry, vol.40, issue.1, pp.69-76, 1991.
DOI : 10.1016/0301-4622(91)85030-T

J. Warrand and H. G. Janssen, Controlled production of oligosaccharides from amylose by acid-hydrolysis under microwave treatment: Comparison with conventional heating, Carbohydrate Polymers, vol.69, issue.2, pp.353-362, 2007.
DOI : 10.1016/j.carbpol.2006.10.021

J. Szejtli, Introduction and General Overview of Cyclodextrin Chemistry, Chemical Reviews, vol.98, issue.5, pp.1743-1754, 1998.
DOI : 10.1021/cr970022c

E. Farkas, L. Janossy, J. Harangi, L. Kandra, and A. Liptak, Synthesis of chromogenic substrates of ??-amylases on a cyclodextrin basis, Carbohydrate Research, vol.303, issue.4, pp.407-415, 1997.
DOI : 10.1016/S0008-6215(97)00187-0

W. S. York, L. K. Harvey, R. Guillen, P. Alberhseim, and A. G. , Structural analysis of tamarind seed xyloglucan oligosaccharides using ??-galactosidase digestion and spectroscopic methods, Carbohydrate Research, vol.248, pp.285-301, 1993.
DOI : 10.1016/0008-6215(93)84135-S

L. Duedahl-olesen, K. M. Kragh, and W. Zimmermann, Purification and characterisation of a malto-oligosaccharide-forming amylase active at high pH from Bacillus clausii BT-21, Carbohydrate Research, vol.329, issue.1, pp.97-107, 2000.
DOI : 10.1016/S0008-6215(00)00153-1

X. Zhu and R. R. Schmidt, New Principles for Glycoside-Bond Formation, Angewandte Chemie International Edition, vol.72, issue.11, pp.1900-1934, 2009.
DOI : 10.1002/(SICI)1099-0690(199811)1998:11<2305::AID-EJOC2305>3.3.CO;2-N

P. Sinaÿ, J. Jacquinet, M. Petitou, P. Duchaussoy, I. Lederman et al., Total synthesis of a heparin pentasaccharide fragment having high affinity for antithrombin III, Carbohydrate Research, vol.132, issue.2, pp.5-9, 1984.
DOI : 10.1016/0008-6215(84)85236-2

O. J. Plante, E. R. Palmacci, and P. H. Seeberger, Automated Solid-Phase Synthesis of Oligosaccharides, Science, vol.291, issue.5508, pp.1523-1527, 2001.
DOI : 10.1126/science.1057324

N. O. Seto, M. M. Palcic, O. Hindsgaul, D. R. Bundle, and S. A. Narang, Expression of a Recombinant Human Glycosyltransferase from a Synthetic Gene and its Utilization for Synthesis of the Human Blood Group B Trisaccharide, European Journal of Biochemistry, vol.5, issue.1, pp.323-328, 1995.
DOI : 10.1016/0304-4157(93)90003-7

M. Lopez, S. Fort, H. Bizot, A. Buléon, and H. Driguez, Chemo-enzymatic synthesis of xylogluco-oligosaccharides and their interactions with cellulose, Carbohydrate Polymers, vol.88, issue.1, pp.185-193, 2012.
DOI : 10.1016/j.carbpol.2011.11.085
URL : https://hal.archives-ouvertes.fr/hal-00720278

T. Antoine, B. Priem, A. Heyraud, L. Greffe, M. Gilbert et al., Large-Scale In Vivo Synthesis of the Carbohydrate Moieties of Gangliosides GM1 and GM2 by Metabolically Engineered Escherichia coli, ChemBioChem, vol.302, issue.5, pp.406-412, 2003.
DOI : 10.1016/S0008-6215(97)00107-9
URL : https://hal.archives-ouvertes.fr/hal-00306904

S. Drouillard, H. Driguez, and E. Samain, Large-Scale Synthesis of H-Antigen Oligosaccharides by ExpressingHelicobacter pylori ??1,2-Fucosyltransferase in Metabolically EngineeredEscherichia coli Cells, Angewandte Chemie International Edition, vol.175, issue.5, pp.1778-1780, 2006.
DOI : 10.1099/00221287-145-11-3245

A. R. Khan, P. Forgo, K. J. Stine, and V. T. Souza, Methods for Selective Modifications of Cyclodextrins, Chemical Reviews, vol.98, issue.5, pp.1977-1996, 1998.
DOI : 10.1021/cr970012b

F. A. Quiocho, Carbohydrate-Binding Proteins: Tertiary Structures and Protein-Sugar Interactions, Annual Review of Biochemistry, vol.55, issue.1, pp.287-315, 1986.
DOI : 10.1146/annurev.bi.55.070186.001443

E. Fischer, Ueber die Glucoside der Alkohole, Berichte der deutschen chemischen Gesellschaft, vol.21, issue.3, pp.2400-2412
DOI : 10.1002/recl.18920110502

R. U. Lemieux and S. Koto, The conformational properties of glycosidic linkages, Tetrahedron, vol.30, issue.13, pp.1933-1944, 1974.
DOI : 10.1016/S0040-4020(01)97324-7

D. K. Roy and M. Bordoloi, Montmorillonite K-10 as a Reusable Catalyst for Fischer Type of Glycosylation under Microwave Irradiation, Journal of Carbohydrate Chemistry, vol.23, issue.4, pp.300-307, 2008.
DOI : 10.1016/S0031-9422(00)85029-3

R. J. Williams, C. E. Paul, and M. Nitz, Protecting-group-free O-glysosidation using p-toluenesulfonohydrazide and glycosyl chloride donors, Carbohydrate Research, vol.386, pp.73-77, 2014.
DOI : 10.1016/j.carres.2013.08.019

K. Yamamoto, T. Tsuji, and T. Osawa, Requirement of the core structure of a complex-type glycopeptide for the binding to immobilized lentil- and pea-lectins, Carbohydrate Research, vol.110, issue.2, pp.283-289, 1982.
DOI : 10.1016/0008-6215(82)84010-X

J. C. Gildersleeve, O. Oyelaran, J. T. Simpson, and B. Allred, Improved Procedure for Direct Coupling of Carbohydrates to Proteins via Reductive Amination, Bioconjugate Chemistry, vol.19, issue.7, pp.1485-1490, 2008.
DOI : 10.1021/bc800153t

T. Yoshida and Y. C. Lee, Glycamine formation via reductive amination of oligosaccharides with benzylamine: efficient coupling of oligosaccharides to protein, Carbohydrate Research, vol.251, pp.175-186, 1994.
DOI : 10.1016/0008-6215(94)84284-1

C. Leteux, R. A. Childs, W. Chai, M. S. Stoll, H. Kogelberg et al., Biotinyl-l-3-(2-naphthyl)-alanine hydrazide derivatives of N-glycans: versatile solid-phase probes for carbohydrate-recognition studies, Glycobiology, vol.8, issue.3, pp.227-236, 1998.
DOI : 10.1093/glycob/8.3.227

S. Peluso, M. De, L. Ufret, M. K. O-'reilly, and B. Imperiali, Neoglycopeptides as Inhibitors of Oligosaccharyl Transferase, Chemistry & Biology, vol.9, issue.12, pp.1323-1328, 2002.
DOI : 10.1016/S1074-5521(02)00281-8
URL : https://doi.org/10.1016/s1074-5521(02)00281-8

S. Park, M. Lee, and I. Shin, Construction of Carbohydrate Microarrays by Using One-Step, Direct Immobilizations of Diverse Unmodified Glycans on Solid Surfaces, Bioconjugate Chemistry, vol.20, issue.1, pp.155-162, 2009.
DOI : 10.1021/bc800442z

A. V. Gudmundsdottir and M. Nitz, Hydrolysis rates of 1-glucosyl-2-benzoylhydrazines in aqueous solution, Carbohydrate Research, vol.342, issue.5, pp.749-752, 2007.
DOI : 10.1016/j.carres.2006.12.015

C. Jiménez-castells, B. De-la-torre, D. Andreu, and R. Gutiérrez-gallego, Neo-glycopeptides: the importance of sugar core conformation in oxime-linked glycoprobes for interaction studies, Glycoconjugate Journal, vol.249, issue.9, pp.879-887, 2008.
DOI : 10.1007/s10719-008-9150-8

M. L. Wolfrom, A. Thompson, and L. W. Georges, RING-CHAIN ISOMERISM IN THE ACETATES OF GALACTOSE OXIME, Journal of the American Chemical Society, vol.54, issue.10, pp.4091-4095, 1932.
DOI : 10.1021/ja01349a038

S. E. Cervigni, P. Dumy, and M. Mutter, Synthesis of Glycopeptides and Lipopeptides by Chemoselective Ligation, Angewandte Chemie International Edition in English, vol.35, issue.11, pp.1230-1232, 1996.
DOI : 10.1002/anie.199612301

F. Peri, P. Dumy, and M. Mutter, Chemo- and stereoselective glycosylation of hydroxylamino derivatives: A versatile approach to glycoconjugates, Tetrahedron, vol.54, issue.40, pp.12269-12278, 1998.
DOI : 10.1016/S0040-4020(98)00763-7

S. Munneke, J. R. Prevost, G. F. Painter, B. L. Stocker, and M. S. Timmer, The Rapid and Facile Synthesis of Oxyamine Linkers for the Preparation of Hydrolytically Stable Glycoconjugates, Organic Letters, vol.17, issue.3, pp.624-627, 2015.
DOI : 10.1021/ol503634j

O. Renaudet, D. Boturyn, and P. Dumy, Biomolecular assembly by iterative oxime ligations, Bioorganic & Medicinal Chemistry Letters, vol.19, issue.14, pp.3880-3883, 2009.
DOI : 10.1016/j.bmcl.2009.03.119
URL : https://hal.archives-ouvertes.fr/hal-01658952

O. Lockhoff and P. Stadler, Syntheses of glycosylamides as glycolipid analogs, Carbohydrate Research, vol.314, issue.1-2, pp.13-24, 1998.
DOI : 10.1016/S0008-6215(98)00278-X

W. Spevak, F. Dasgupta, C. J. Hobbs, and J. O. Nagy, -Allylglycosylamides from Unprotected Carbohydrates, The Journal of Organic Chemistry, vol.61, issue.10, pp.3417-3422, 1996.
DOI : 10.1021/jo9522522

F. Pérez-balderas, M. Ortega-muñoz, J. Morales-sanfrutos, F. Hernández-mateo, F. G. Calvo-flores et al., Multivalent Neoglycoconjugates by Regiospecific Cycloaddition of Alkynes and Azides Using Organic-Soluble Copper Catalysts, Organic Letters, vol.5, issue.11, pp.1951-1954, 2003.
DOI : 10.1021/ol034534r

S. Halila, M. Manguian, S. Fort, S. Cottaz, T. Hamaide et al., Syntheses of Well-Defined Glyco-Polyorganosiloxanes by ???Click??? Chemistry and their Surfactant Properties, Macromolecular Chemistry and Physics, vol.3, issue.12, pp.1282-1290, 2008.
DOI : 10.1002/macp.200700629
URL : https://hal.archives-ouvertes.fr/hal-00303844

H. C. Kolb, M. G. Finn, and K. B. Sharpless, Click Chemistry: Diverse Chemical Function from a Few Good Reactions, Angewandte Chemie International Edition, vol.36, issue.6, pp.2004-2021, 2001.
DOI : 10.1016/B978-008096518-5.00095-2

R. Huisgen, Kinetics and Mechanism of 1,3-Dipolr Cycloadditions, Angewandte Chemie International Edition in English, vol.77, issue.11, pp.633-645, 1963.
DOI : 10.1002/recl.19510701109

C. W. Tornøe, C. Christensen, and M. , Peptidotriazoles on Solid Phase:?? [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides, The Journal of Organic Chemistry, vol.67, issue.9, pp.3057-3064, 2002.
DOI : 10.1021/jo011148j

G. Pourceau, A. Meyer, Y. Chevolot, E. Souteyrand, J. Vasseur et al., Oligonucleotide Carbohydrate-Centered Galactosyl Cluster Conjugates Synthesized by Click and Phosphoramidite Chemistries, Bioconjugate Chemistry, vol.21, issue.8, pp.1520-1529, 2010.
DOI : 10.1021/bc1001888
URL : https://hal.archives-ouvertes.fr/hal-00519471

F. Fazio, M. C. Bryan, O. Blixt, J. C. Paulson, and C. Wong, Synthesis of Sugar Arrays in Microtiter Plate, Journal of the American Chemical Society, vol.124, issue.48, pp.14397-14402, 2002.
DOI : 10.1021/ja020887u

L. D. Pachón, J. H. Van-maarseveen, and G. Rothenberg, Click Chemistry: Copper Clusters Catalyse the Cycloaddition of Azides with Terminal Alkynes, Advanced Synthesis & Catalysis, vol.4, issue.6, pp.811-815, 2005.
DOI : 10.1002/adsc.200404383

I. S. Park, M. S. Kwon, Y. Kim, J. S. Lee, and J. Park, Heterogeneous Copper Catalyst for the Cycloaddition of Azides and Alkynes without Additives under Ambient Conditions, Organic Letters, vol.10, issue.3, pp.497-500, 2008.
DOI : 10.1021/ol702790w

A. Dumont, A. Malleron, M. Awwad, S. Dukan, and B. Vauzeilles, Click-Mediated Labeling of Bacterial Membranes through Metabolic Modification of the Lipopolysaccharide Inner Core, Angewandte Chemie International Edition, vol.17, issue.13, pp.3143-3146, 2012.
DOI : 10.1016/j.copbio.2005.12.006

M. C. Cortizo and M. F. Lorenzo-de-mele, Cytotoxicity of Copper Ions Released from Metal: Variation with the Exposure Period and Concentration Gradients, Biological Trace Element Research, vol.102, issue.1-3, pp.129-141, 2004.
DOI : 10.1385/BTER:102:1-3:129

N. J. Agard, J. A. Prescher, C. R. Bertozzi, and J. Am, A Strain-Promoted [3 + 2] Azide???Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems, Journal of the American Chemical Society, vol.126, issue.46, pp.15046-15047, 2004.
DOI : 10.1021/ja044996f

D. H. Ess, G. O. Jones, and K. N. Houk, Transition States of Strain-Promoted Metal-Free Click Chemistry:?? 1,3-Dipolar Cycloadditions of Phenyl Azide and Cyclooctynes, Organic Letters, vol.10, issue.8, pp.1633-1636, 2008.
DOI : 10.1021/ol8003657

J. A. Codelli, J. M. Baskin, N. J. Agard, and C. R. Bertozzi, Second-Generation Difluorinated Cyclooctynes for Copper-Free Click Chemistry, Journal of the American Chemical Society, vol.130, issue.34, pp.11486-11493, 2008.
DOI : 10.1021/ja803086r
URL : http://pubs.acs.org/doi/pdf/10.1021/ja803086r

M. Meldal and C. W. Tornøe, Cu-Catalyzed Azide???Alkyne Cycloaddition, Chemical Reviews, vol.108, issue.8, pp.2952-3015, 2008.
DOI : 10.1021/cr0783479

S. Bräse, C. Gil, K. Knepper, and V. Zimmermann, Organic Azides: An Exploding Diversity of a Unique Class of Compounds, Angewandte Chemie International Edition, vol.127, issue.33, pp.5188-5240, 2005.
DOI : 10.1021/jp045254b

Q. Zhang, F. Zhou, Y. Ye, G. Xia, M. L. Wu et al., -Tosylhydrazones, Alkynes and Azides: Synthesis of Trisubstituted 1,2,3-Triazoles, Advanced Synthesis & Catalysis, vol.74, issue.10, pp.2277-2286, 2010.
DOI : 10.1021/jo802078f

F. C. Plancher, Atti reale accad. naz Lincei, p.489, 1904.

P. O. Tawney, R. H. Snyder, C. E. Bryan, R. P. Conger, F. S. Dovell et al., The Chemistry of Maleimide and Its Derivatives. I. N-Carbamylmaleimide, The Journal of Organic Chemistry, vol.25, issue.1, pp.56-60, 1960.
DOI : 10.1021/jo01071a017

D. H. Rich, P. D. Gesellchen, D. Tong, A. Cheung, and C. K. Buckner, Alkylating derivatives of amino acids and peptides. Synthesis of N-maleoylamino acids, [1-(N-maleoylglycyl)cysteinyl]oxytocin, and [1-(N-maleoyl-11-aminoundecanoyl)cysteinyl]oxytocin. Effects on vasopressin-stimulated water loss from isolated toad bladder, Journal of Medicinal Chemistry, vol.18, issue.10, pp.1004-1010, 1975.
DOI : 10.1021/jm00244a011

C. E. Hoyle and C. N. Bowman, Thiol-Ene Click Chemistry, Angewandte Chemie International Edition, vol.42, issue.2, pp.1540-1573, 2010.
DOI : 10.1021/ma9009627

A. B. Lowe, Thiol-ene ???click??? reactions and recent applications in polymer and materials synthesis, Polym. Chem., vol.131, issue.1, pp.17-36, 2010.
DOI : 10.1021/ja809345d

J. Ni, S. Singh, and L. Wang, Synthesis of Maleimide-Activated Carbohydrates as Chemoselective Tags for Site-Specific Glycosylation of Peptides and Proteins, Bioconjugate Chemistry, vol.14, issue.1, pp.232-238, 2003.
DOI : 10.1021/bc025617f

O. Diels and K. Alder, Synthesen in der hydroaromatischen Reihe, Justus Liebig's Annalen der Chemie, vol.29, issue.1, pp.98-122, 1928.
DOI : 10.1039/CT8844500410

O. Diels, K. Alder, and . Ber, Synthesen in der hydroaromatischen Reihe, IV. Mitteilung: ??ber die Anlagerung von Maleins??ure-anhydrid an arylierte Diene, Triene und Fulvene (Mitbearbeitet von Paul Pries), Berichte der deutschen chemischen Gesellschaft (A and B Series), vol.60, issue.8, pp.2081-2087, 1929.
DOI : 10.1002/cber.19270600227

J. Sauer and R. Sustmann, Mechanistic Aspects of Diels-Alder Reactions: A Critical Survey, Angewandte Chemie International Edition in English, vol.80, issue.10, pp.779-807, 1980.
DOI : 10.1246/nikkashi1898.66.10_1442

R. B. Woodward and R. Hoffmann, Die Erhaltung der Orbitalsymmetrie, Angewandte Chemie, vol.90, issue.21, pp.797-869, 1969.
DOI : 10.1007/BFb0050698

K. N. Houk, Frontier molecular orbital theory of cycloaddition reactions, Accounts of Chemical Research, vol.8, issue.11, pp.361-369, 1975.
DOI : 10.1021/ar50095a001

V. Pozsgay, Type 1, The Journal of Organic Chemistry, vol.63, issue.17, pp.5983-5999, 1998.
DOI : 10.1021/jo980660a

I. Otsuka, S. Tallegas, Y. Sakai, C. Rochas, S. Halila et al., Control of 10 nm scale cylinder orientation in self-organized sugar-based block copolymer thin films, Nanoscale, vol.43, issue.7, pp.2637-2641, 2013.
DOI : 10.1021/ma1012946
URL : https://hal.archives-ouvertes.fr/hal-00825424

L. Mazzarino, G. Loch-neckel, L. D. Bubniak, S. Mazzucco, M. C. Santos-silva et al., Curcumin-Loaded Chitosan-Coated Nanoparticles as a New Approach for the Local Treatment of Oral Cavity Cancer, Journal of Nanoscience and Nanotechnology, vol.15, issue.1, pp.781-791, 2015.
DOI : 10.1166/jnn.2015.9189

A. Ghaffar, A. Scott, and G. Scott, The chemical and physical changes occurring during U.V. degradation of high impact polystyrene, European Polymer Journal, vol.11, issue.3, pp.271-275, 1975.
DOI : 10.1016/0014-3057(75)90075-0

A. Petrelli, R. Borsali, S. Fort, and S. Halila, Oligosaccharide-based block copolymers: Metal-free thiol???maleimide click conjugation and self-assembly into nanoparticles, Carbohydrate Polymers, vol.124, pp.109-116, 2015.
DOI : 10.1016/j.carbpol.2015.01.079

J. K. Kim, S. Y. Yang, Y. Lee, and Y. Kim, Functional nanomaterials based on block copolymer self-assembly, Progress in Polymer Science, vol.35, issue.11, pp.1325-1349, 2010.
DOI : 10.1016/j.progpolymsci.2010.06.002

S. I. Hong, C. Presolski, M. G. Ma, F. Finn, P. Wolbers et al., Analysis and Optimization of Copper-Catalyzed Azide??????Alkyne Cycloaddition for Bioconjugation, Angewandte Chemie International Edition, vol.28, issue.112, pp.9879-9883, 2006.
DOI : 10.1007/BF01242085

C. E. Hoyle, A. B. Lowe, and C. N. Bowman, Thiol-click chemistry: a multifaceted toolbox for small molecule and polymer synthesis, Chemical Society Reviews, vol.8, issue.24, pp.1355-1387, 2010.
DOI : 10.1021/ja809345d

S. P. Koo, M. M. Stamenovi?, R. A. Prasath, A. J. Inglis, F. E. Du-prez et al., Limitations of radical thiol-ene reactions for polymer-polymer conjugation, Journal of Polymer Science Part A: Polymer Chemistry, vol.42, issue.8, pp.1699-1713, 2010.
DOI : 10.1002/anie.200805993

G. Li, R. K. Randev, A. H. Soeriyadi, G. Rees, C. Boyer et al., Investigation into thiol-(meth)acrylate Michael addition reactions using amine and phosphine catalysts, Polymer Chemistry, vol.39, issue.8, pp.1196-1204, 2010.
DOI : 10.1002/masy.19961110106

C. Tsai, C. Lin, H. Tsai, C. Chen, W. Li et al., The Immunologically Active Oligosaccharides Isolated from Wheatgrass Modulate Monocytes via Toll-like Receptor-2 Signaling, Journal of Biological Chemistry, vol.270, issue.24, pp.17689-17697, 2013.
DOI : 10.1016/j.humimm.2011.08.015
URL : http://www.jbc.org/content/288/24/17689.full.pdf

L. T. Nguyen, M. T. Gokmen, and F. E. Prez, Kinetic comparison of 13 homogeneous thiol???X reactions, Polymer Chemistry, vol.25, issue.22, pp.5527-5536, 2013.
DOI : 10.1002/pola.1987.080250919

H. Maeda, J. Wu, T. Sawa, Y. Matsumura, and K. Hori, Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review, Journal of Controlled Release, vol.65, issue.1-2, pp.271-284, 2000.
DOI : 10.1016/S0168-3659(99)00248-5

D. Mather, K. Viswanathan, K. M. Miller, and T. E. Long, Michael addition reactions in macromolecular design for emerging technologies, Progress in Polymer Science, vol.31, issue.5, pp.487-531, 2006.
DOI : 10.1016/j.progpolymsci.2006.03.001

M. E. Smith, F. F. Schumacher, C. P. Ryan, L. M. Tedaldi, D. Papaioannou et al., Protein Modification, Bioconjugation, and Disulfide Bridging Using Bromomaleimides, Journal of the American Chemical Society, vol.132, issue.6, pp.1960-1965, 2010.
DOI : 10.1021/ja908610s
URL : https://doi.org/10.1021/ja908610s

D. H. Rich, P. D. Gesellchen, A. Tong, A. Cheung, and C. K. Buckner, Alkylating derivatives of amino acids and peptides. Synthesis of N-maleoylamino acids, [1-(N-maleoylglycyl)cysteinyl]oxytocin, and [1-(N-maleoyl-11-aminoundecanoyl)cysteinyl]oxytocin. Effects on vasopressin-stimulated water loss from isolated toad bladder, Journal of Medicinal Chemistry, vol.18, issue.10, pp.1004-1010, 1975.
DOI : 10.1021/jm00244a011

G. W. Hart and R. J. Copeland, Glycomics Hits the Big Time, Cell, vol.143, issue.5, pp.672-676, 2010.
DOI : 10.1016/j.cell.2010.11.008
URL : https://doi.org/10.1016/j.cell.2010.11.008

T. Antoine, C. Bosso, A. Heyraud, and E. Samain, Large scale in vivo synthesis of globotriose and globotetraose by high cell density culture of metabolically engineered Escherichia coli, Biochimie, vol.87, issue.2, pp.197-203, 2005.
DOI : 10.1016/j.biochi.2004.10.010
URL : https://hal.archives-ouvertes.fr/hal-00305969

C. Dumon, C. Bosso, J. P. Utille, A. Heyraud, and E. Samain, Production of Lewis x Tetrasaccharides by Metabolically Engineered Escherichia coli, ChemBioChem, vol.194, issue.2, pp.359-365, 2006.
DOI : 10.1016/0008-6215(89)85007-4
URL : https://hal.archives-ouvertes.fr/hal-00305827

A. Lohse, R. Martins, M. R. Jørgensen, and O. Hindsgaul, Solid-Phase Oligosaccharide Tagging (SPOT): Validation on Glycolipid-Derived Structures, Angewandte Chemie International Edition, vol.1067, issue.25, pp.4167-4172, 2006.
DOI : 10.1016/S0304-4165(99)00165-8

H. Akizawa, M. Imajima, H. Hanaoka, T. Uehara, S. Satake et al., Renal Brush Border Enzyme-Cleavable Linkages for Low Renal Radioactivity Levels of Radiolabeled Antibody Fragments, Bioconjugate Chemistry, vol.24, issue.2, pp.291-299, 2013.
DOI : 10.1021/bc300428b

B. Svensson, K. Larsen, and A. Gunnarsson, Characterization of a glucoamylase G2 from Aspergillus niger, European Journal of Biochemistry, vol.19, issue.3, pp.497-502, 1986.
DOI : 10.1128/MCB.4.11.2306