A method for the selective reduction of carbohydrate 4,6-O-benzylidene acetals
- 1 January 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (5) , 669-672
- https://doi.org/10.1016/0040-4039(94)02348-f
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Recent progress in O-glycosylation methods and its application to natural products synthesisChemical Reviews, 1993
- Carbohydrate differentiation antigens: probable ligands for cell adhesion moleculesTrends in Biochemical Sciences, 1991
- Glycobiology: a growing field for drug designTrends in Pharmacological Sciences, 1991
- Acetal-bond Cleavage of 4,6-O-Alkylidenehexopyranosides by Diisobutylaluminium Hydride and by Lithium Triethylborohydride-TiCl4Chemistry Letters, 1987
- New Methods for the Synthesis of Glycosides and Oligosaccharides—Are There Alternatives to the Koenigs‐Knorr Method? [New Synthetic Methods (56)]Angewandte Chemie International Edition in English, 1986
- Regioselective reductive ring opening of 4-methoxybenzylidene acetals of hexopyranosides. Access to a novel protective group strategyJournal of the Chemical Society, Chemical Communications, 1984
- Reductive Ring Openings of Carbohydrate Benzylidene Acetals Using Borane-Trimethylamine and Aluminium Chloride. Regioselectivity and Solvent DependanceJournal of Carbohydrate Chemistry, 1983
- Reductive cleavage of glycosidesJournal of the American Chemical Society, 1982
- HYDROSILANES AS REDUCING AGENTS. A REVIEWOrganic Preparations and Procedures International, 1980
- Applications of Ionic Hydrogenation to Organic SynthesisSynthesis, 1974