Synthesis of a new antimicrobial aminoglycoside employing maltose as a key starting material
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (25) , 2871-2874
- https://doi.org/10.1016/s0040-4039(00)96231-2
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Displacement of “pseudoanomeric” hydroxyl groups by using the diethyl azodicarboxylate-triphenylphosphine systemCarbohydrate Research, 1986
- α-Glucosidasen-Inhibitoren, 3. 4-Alkylamino-4,6-didesoxyzucker durch reduktive AminierungEuropean Journal of Organic Chemistry, 1985
- Discrimination between the 2,3- and the 2′,3′-hydroxyl groups of maltose and cellobiose through their specific protectionCarbohydrate Research, 1985
- A Convenient One-Step Synthesis of Glycidyl EthersSynthesis, 1983
- Synthesis of amylostatin (XG), α-glucosidase inhibitor with basic pseudotrisaccharide structureTetrahedron Letters, 1982
- Lanthanoids in organic synthesis. 6. Reduction of .alpha.-enones by sodium borohydride in the presence of lanthanoid chlorides: synthetic and mechanistic aspectsJournal of the American Chemical Society, 1981
- Chemistry of the glycosidic linkage. Direct conversion of glycosides into 1-thioglycosides by use of [alkyl(or aryl)thio]trimethylsilanesCarbohydrate Research, 1980
- Unsaturated carbohydrates. Part 21. A carbocyclic ring closure of a hex-5-enopyranoside derivativeJournal of the Chemical Society, Perkin Transactions 1, 1979
- Fortimicins A and B, new aminoglycoside antibiotics. III. Structural identification.The Journal of Antibiotics, 1977
- The reduction of azides with sodium borohydride: a convenient synthesis of methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-d-allopyranosideCarbohydrate Research, 1967