ChemInform Abstract: Synthesis of Thio-Linked Analogues of Lewis X and Sialyl Lewis X.
β Scribed by T. EISELE; R. R. SCHMIDT
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 23 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable via the βReferencesβ option.
π SIMILAR VOLUMES
The decasaccharide sialyl-trimeric-Lewis x is a component of glycoproteins and glycolipids that serve as E-and P-selectin ligands. The synthesis of this target structure was accomplished by utilizing a combination of chemical and enzymatic methods. Highlights of the chemical synthesis include minima
Synthesis of a Thio-Analogue of Lewis X by Regioselective Opening of Cyclic Sulfamidates. -The synthesis of the title analogue (I) contains linking of galactose and allosamine, protected by a p-methoxyphenyl group at O-6 (higher yield), transformation into cyclic sulfamidate, and its regioselective