IPCM


Partenaires

UPMC
CNRS




Accueil du site > Les équipes > Glycochimie Organique Biologique et Supramoléculaire (GOBS) > Thèmes de recherche > Synthèse totale et méthodologie

Synthèse totale et méthodologie







Stereochemical Assignment and First Synthesis of the Core of Miharamycin Antibiotics
Chem. Eur. J. 2008, 14, 10066-10073





Phenylenediamine catalysis of “click glycosylations” in water : practical and direct access to unprotected neoglycoconjugates
Org. Biomol. Chem., 2008, 6, 1898-1901





Alkylalanes and methyl furanosides : regioselective de-O-benzylation or acetal cleavage
Carbohydr. Res. 2006, 341, 2135-3144





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





Trimethylaluminium (TMAL) promoted rearrangements of unsaturated sugars into cyclohexanes
Tetrahedron : Asymm., 2004, 15, 699-703





Diisobutylaluminium hydride (DIBAL-H) as a molecular scalpel : a new mechanistic proposal for a spiroketal rearrangement
Tetrahedron Lett. 2004, 45, 8165-8168





Triisobutylaluminium and diisobutylaluminium hydride as molecular scalpels :
the regioselective stripping of perbenzylated sugars and cyclodextrins

Chem. Eur. J., 2004, 10, 2960-2971









Synthesis of (E)- and (Z)-exo-methoxyglycal methyl pyranosides and study of their reactivity towards Lewis acids
Eur. J. Org. Chem., 2003, 14, 2678-2683





Triisobutylaluminium promoted reductive rearrangement of substituted vinyl ethers to homologous alcohols
Chem. Commun., 2000, 1507-1508





Carbocyclic Ring Closure of Unsaturated S-, Se- and C- Aryl Glycosides
Angew. Chem., Int. Ed. Engl., 2000, 39, 362-364





Regioselective debenzylation of sugars using triisobutylaluminium
C.R. Acad. Sci. Paris, t. 2, Série II c, 1999, 441-448