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RESEARCH PRODUCT
Stereoselective glycosylation of Alcohols and Silyl Ethers Using Glycosyl Fluorides and Boron Trifluoride Etherate
Wilfried SagerHorst Kunzsubject
inorganic chemicalschemistry.chemical_classificationanimal structuresGlycosylationSilylationChemistryOrganic ChemistryAlcoholEthermacromolecular substancesFuranoseBiochemistryCatalysiscarbohydrates (lipids)Inorganic Chemistrychemistry.chemical_compoundPyranoseDrug DiscoveryOrganic chemistrylipids (amino acids peptides and proteins)GlycosylPhysical and Theoretical ChemistryBoron trifluoridedescription
The stereoselective glycosylation of alcohols and their silyl ethers has been achieved using O-alkyl-, O-acyl-, and acetal-protected glycosyl fluorides of the pyranose and furanose series and boron trifluoride etherate in CH2Cl2.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 1985-02-13 | Helvetica Chimica Acta |