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Accueil > Les équipes > Glycochimie Organique Biologique et Supramoléculaire (GOBS) > Thèmes de recherche

Cyclodextrines

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Cyclodextrin Polyrotaxanes as a highly modular platform for the development of imaging agents
Chem. Eur. J. 2014, 20, 10915-10920

Primary, Secondary and Tertiary Azido Interactions build-up solid-state hierarchical Cyclodextrin-Based Supramolecular Polymer
Angew. Chem. Int. Ed. 2014, 53, 7238-7242

Cyclodextrin-adamantane conjugates, self-inclusion and aggregation versus supramolecular polymer formation
Org. Chem. Frontiers 2014, 1, 703-706

Beta cyclodextrins bind, stabilize and remove lipofuscin bisretinoids from retinal pigment epithelium
Proc. Natl. Acad. Sci. U.S.A. 2014, 111, 1402-1408

Site-selective hetero-functionalization of Cyclodextrins, discovery, development and use for catalysis
Synlett 2013, 2629-2640

NHC-Capped Cyclodextrins (ICyDs) : Insulated Metal Complexes, Comutable Multicoordination Sphere and Cavity-Dependant Catalytisis,
Angew. Chem. Int. Ed. 2013, 52, 7213-7218

Diametrically opposed Carbenes on an α-Cyclodextrin : synthesis, characterization of organometallic complexes and Suzuki-Miyaura coupling in ethanol and in water, Eur. J. Org. Chem. 2013, DOI : 10.1002/ejoc.201300268

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An “Against-the-Rules” Double Bank Shot with Diisobutylaluminium Hydride allows Triple Functionalisation of α-Cyclodextrin, Angew. Chem. Int. Ed. 2013, 52, 639-644

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Cyclodextrin-Induced Auto-healing of Hybrid Polyoxometalates, Angew. Chem. Int. Ed., 2012, 51, 487-490– Hot Paper

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Cyclodextrins selectively modified on both rims using an O-3-debenzylative post-functionalisation, a consequence of the Sorrento meeting, Carbohydr. Res. 2012, 356 278–281

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Cavitand supported Tetraphosphine : Cyclodextrin offers a useful platform for Suzuki-Miyaura cross-coupling, Chem. Commun., 2011, 47, 9206-9208 – Editor’s choice in ChemInform 2011, 42, issue 48

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N-Heterocyclic Carbene Ligand based on a ß-cyclodextrin-Imidazolium Salt : Synthesis, Characterization of Organometallic Complexes and Suzuki Coupling, New J. Chem. 2011, 35, 2061–2065

PNG - 38.4 ko

Synthesis and Electrochemical Study of an Original Copper(II)-capped Salen-Cyclodextrin Complex, Eur. J. Inorg. Chem. 2010, 29, 4720–4727

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Duplex of capped-cyclodextrins, synthesis and cross-linking behaviour with a biopolymer, Org. Biomol. Chem., 2010, 8, 3437-3443

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Can hetero-polysubstituted cyclodextrins be considered as inherently chiral concave molecules ?
Angew. Chem. Int. Ed. 2010, 49, 2314-2318

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Cyclodextrin tetraplexes : first syntheses and potential as cross-linking agent
Chem. Commun., 2010, 46, 2238–2240

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Diisobutylaluminum hydride (DIBAL-H) promoted secondary rim regioselective demethylations of permethylated β-cyclodextrin : a mechanistic proposal
Eur. J. Org. Chem., 2010, 1510–1516

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µ-Waves Avoid Large Excesses of Diisobutyl-aluminium-hydride (DIBAL-H) in the
Debenzylation of Perbenzylated α-Cyclodextrin

Tetrahedron Lett. 2010, 51, 1254-1256

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Cap-induced synthesis of hetero-trifunctional cyclodextrins, from flamingo-cap to bascule-bridge
Eur. J. Org. Chem., 2009, 1295-1303

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Surgical Regiospecific Tandem Azide-reduction/deprotection to afford versatile Amino alcohol-α- and β-Cyclodextrins
Angew. Chem. Int. Ed. 2008, 47, 7060-7063

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Multiple homo and hetero-functionalisations of α-cyclodextrin through oriented deprotections
J. Org. Chem. 2008, 73, 2819-2828

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Hydrophilic duplex cyclodextrin forming supramolecular assemblies by physical cross-linking of a biopolymer
Chem. Eur. J. 2007, 13, 8847 –8857

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img19 Bascule-bridge or deoxy-sugars : two ways to tridifferentiate α- and β-cyclodextrins in a clockwise manner
Chem. Eur. J., 2007, 13, 9757-9774

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Amphiphilic Bipolar Duplex α-Cyclodextrin Forming Vesicles
Tetrahedron, 2007, 63, 2973-2977

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Sequential Ring Closing/Opening Metathesis for the Highly Selective Synthesis of a Triply Bifunctionalized α-Cyclodextrin
Chem. Commun., 2006, 1112-1114

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Expeditious Selective Synthesis of Primary Rim Tri-differentiated α-Cyclodextrin
Tetrahedron Lett. 2006, 47, 4137-4139

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Pd-catalysed Capping Removal on a Tri-differentiated α-Cyclodextrin
Chem. Lett., 2006, 35, 534-535

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Diisobutylaluminium hydride (DIBAL-H) is promoting a selective clockwise debenzylation of perbenzylated 6A, 6D-dideoxy-α-Cyclodextrin
Tetrahedron Lett. 2005, 46, 7757-7760

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The first chemical synthesis of a cyclodextrin heteroduplex
Chem. Biodiv., 2004, 1, 129-137

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img20 Triisobutylaluminium and diisobutylaluminium hydride as molecular scalpels : the regioselective stripping of perbenzylated sugars and cyclodextrins
Chem. Eur. J., 2004, 10, 2960-2971

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