HIGHLY STEREOSELECTIVE SYNTHESIS OF α-d-GLUCOPYRANOSIDES BY THE N-IODOSUCCINIMIDE-PROMOTED INTERNAL CYCLIZATION
- 5 October 1982
- journal article
- research article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 11 (10) , 1525-1528
- https://doi.org/10.1246/cl.1982.1525
Abstract
Highly stereoselective cyclizations of hydroxy enol ethers are effected by N-iodosuccinimide to result in the exclusive formation of 2′-deoxy-2′-iodo-α-D-glucopyranosides. An analog of glycolipid is also successfully synthesized according to the present method.Keywords
This publication has 4 references indexed in Scilit:
- Advances in Selective Chemical Syntheses of Complex OligosaccharidesAngewandte Chemie International Edition in English, 1982
- Removal of O-benzyl protecting-groups of carbohydrate derivatives by catalytic, transfer hydrogenationCarbohydrate Research, 1980
- Studies on unsaturated sugars with particular reference to the synthesis of 6-Deoxy-6-fluoro derivativesAustralian Journal of Chemistry, 1976
- Glycosyl GlyceridesPublished by Elsevier ,1974