Glycosyl-inositol deivatives II. Synthesis of 2-amino-2-deoxy-D galactosyl-α-1,3-D-chiro-inositol
✍ Scribed by William K Berlin; Sho-Nong Wang; T.Y Shen
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 221 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The "aside method" has been applied to the preparation of a 2amino-2-deoxy-a-Q-galactosyl-Q-m-inositol disaccharide, using silver perchlorate and silver carbonate as the coupling reaction catalysts. A family of glycosyl phosphatidyl inositols (GPI) has been recognized recently as versatile anchor systems for various cell-surface proteins, including enzymes, receptors, antigens and immunological factors.' The generic structure of GPI may be depicted as: Phosphatidyl inositol-hexosamine-hexoses-mannose-6-phosphate--protein a.
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## 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 “Full Text” option. The original article is trackable v
A convenient preparative synthesis of 1-D-6-O-(2-amino-2deoxy-α-D-glycopyranosyl)-chiro-inositol 1-phosphate (III) and -1,2-cyclic phosphate (IV) using D-chiro-inositol as starting material is reported.