Synthesis of β-O-glycosides using enol ether and imidate derived leaving groups. Emphasis on the use of nitriles as a solvent
- 1 January 1991
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 47 (48) , 9985-9992
- https://doi.org/10.1016/s0040-4020(01)96047-8
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Nitriles as Solvents in Glycosylation Reactions: Highly Selective β-Glycoside Synthesis1Synlett, 1990
- A rapid and efficient synthesis of 1,2-trans-β-linked glycosides via benzyl- or benzoyl-protected glycopyranosyl phosphatesJournal of the Chemical Society, Chemical Communications, 1989
- Direct elaboration of pent-4-enyl glycosides into disaccharidesJournal of the Chemical Society, Chemical Communications, 1988
- Sulfenate esters as glycosyl acceptors: A novel approach to O-glycosides from thioglycosides and sulfenate estersTetrahedron Letters, 1987
- The Application of the Trichloroacetimidate Method to the Synthesis of α-D-Gluco- and α-D-GalactopyranosidesJournal of Carbohydrate Chemistry, 1987
- O-(α-D-Glucopyranosyl)trichloroacetimidate as a Glucosyl DonorJournal of Carbohydrate Chemistry, 1985
- On the stereochemical control of glycosylation reactions by the addition of tetrahydrofuranCarbohydrate Research, 1979
- Über die orthoesterbildung als konkurrenzreaktion zur glykosylierungCarbohydrate Research, 1977
- Results and Problems of O‐Glycoside SynthesisAngewandte Chemie International Edition in English, 1974
- Ergebnisse und Probleme der O‐GlykosidsyntheseAngewandte Chemie, 1974