Substrates for the differentiation of the N-acetylglucosaminytransferases. Synthesis of βDGlcNAc(1 → 2)αDMan(1 → 6)βDMan and βDGlcNAc(1 → 2)αDMan(1 → 6) [αDMan(1 → 3)]βDMan glycosides
- 1 September 1986
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 64 (9) , 1771-1780
- https://doi.org/10.1139/v86-292
Abstract
The trisaccharide βDGlcNAc(1 → 2)αDMan(1 → 6)βDMan (2) and the tetrasaccharide βDGlcNAc(1 → 2)αDMan(1 → 6)[αDMan(1 → 3)]βDMan (3) have been chemically synthesized as their 8-methoxycarbonyloctyl glycosides. Compounds 2 and 3, both partial structures of naturally occurring asparagine linked oligosaccharides, are designed to function as selective substrates in N-acetylglucosaminytransferase assays.This publication has 2 references indexed in Scilit:
- Bausteine von Oligosacchariden, XXX. Neue effektive β‐Glycosidsynthese für Mannose‐Glycoside Synthesen von Mannose‐haltigen OligosaccharidenEuropean Journal of Inorganic Chemistry, 1981
- Synthesis of 2-Amino-2-deoxy-β-D-glucopyranosidesPublished by American Chemical Society (ACS) ,1977