Stereoselective glycosylation of Alcohols and Silyl Ethers Using Glycosyl Fluorides and Boron Trifluoride Etherate
- 12 February 1985
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 68 (1) , 283-287
- https://doi.org/10.1002/hlca.19850680134
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Die Allylgruppe als mild und selektiv abspaltbare Carboxy-Schutzgruppe zur Synthese empfindlicherO-GlycopeptideAngewandte Chemie, 1984
- Reactions of glycosyl fluorides. Synthesis of O-, S-, and N-glycosidesJournal of the Chemical Society, Chemical Communications, 1984
- The Allyl Group as Mildly and Selectively Removable Carboxy‐Protecting Group for the Synthesis of Labile O‐GlycopeptidesAngewandte Chemie International Edition in English, 1984
- Haworth Memorial Lecture. Synthesis of complex oligosaccharide chains of glycoproteinsChemical Society Reviews, 1984
- Synthese und Reaktionen der 3-O-Phosphoniogluco-und -allofuranosenEuropean Journal of Organic Chemistry, 1982
- Glycosidsynthese mit 2,3,4,6‐Tetra‐O‐pivaloyl‐α‐D‐glucopyrancsylbromidEuropean Journal of Organic Chemistry, 1982
- AN EFFICIENT METHOD FOR GLUCOSYLATION OF HYDROXY COMPOUNDS USING GLUCOPYRANOSYL FLUORIDEChemistry Letters, 1981
- Chemistry of the glycosidic linkage. An efficient synthesis of 1,2-trans-di-saccharidesCarbohydrate Research, 1977
- Reaktionen mit phosphororganischen Verbindungen. XLI[1]. Neuartige synthetische Aspekte des Systems Triphenylphosphin‐Azodicarbonsäureester‐HydroxyverbindungHelvetica Chimica Acta, 1976
- Triphenylphosphine oxide complexes of non-transition metal halidesJournal of Inorganic and Nuclear Chemistry, 1963