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

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

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

µ-Waves Avoid Large Excesses of Diisobutyl-aluminium-hydride (DIBAL-H) in the Debenzylation of Perbenzylated α-Cyclodextrin
Tetrahedron Lett. 2010, 51, 1254-1256

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

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

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

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

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

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

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

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

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

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

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

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