Stannous triflate mediated glycosidations. A stereoselective synthesis of 2-amino 2-deoxy-β-D-glucopyranosides directly with the natural N-acetyl protecting group.
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (42) , 5041-5044
- https://doi.org/10.1016/s0040-4039(00)96690-5
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Cell surface carbohydrates: molecules in search of a function?Journal of Cell Science, 1986
- The -allyloxycarbonyl derivative of -glucosamine: a potent precursor of β-glycosidation.Tetrahedron Letters, 1986
- Stannous triplate mediated glycosidations. A sterroselective synthesis of β -dTetrahedron Letters, 1985
- Protected glycosides and disaccharides of 2-amino-2-deoxy-d-glucopyranose by ferric chloride-catalyzed couplingCarbohydrate Research, 1985
- Synthetic control leading to chiral compoundsTetrahedron, 1984
- Synthesis of 2-Amino-2-deoxy-β-D-glucopyranosidesPublished by American Chemical Society (ACS) ,1977