The title trisaccharide glycosides were needed for studies of the interactions of &tins, receptor sites for bacteriophages with Salmonella lipopolysaccharide corespecificity, and correlation of n.m.r. chemical shifts and structure. The methods used in the syntheses were conventional. Thus, 2,3,4,6-
✦ LIBER ✦
α-D-Mannosidase-catalyzed hydrolysis of substituted phenyl α-D-mannopyranosides
✍ Scribed by Jozef De Prijker; André De Bock; Clement K. De Bruyne
- Book ID
- 108308350
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- English
- Weight
- 898 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0008-6215
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During the preparation of simple mannopyranosides using the Koenigs-Knorr type reaction, we observed that a significant amount of disaccharide glycoside was produced when the alcohol was used in amounts less than equivalent of 2,3,4,6-tetra-O-acetyl-c~-D-mannopyranosyl bromide ("acetobromomannose").