𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Asymmetric acetalation of α,α-trehalose: Synthesis of α-d-galactopyranosyl α-d-glucopyranoside and 6-deoxy-6-fluoro-α-d-glucopyranosyl α-d-glucopyranoside

✍ Scribed by Jacques Defaye; Hugues Driguez; Bernard Henrissat; Jacques Gelas; Edith Bar-Guilloux

Book ID
108307762
Publisher
Elsevier Science
Year
1978
Tongue
English
Weight
668 KB
Volume
63
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of methyl 3-O-α-d-galactopyran
Synthesis of methyl 3-O-α-d-galactopyranosyl-6-O-α-d-mannopyranosyl-α-d-mannopyranoside, methyl 3-O-α-d-glucopyranosyl-6-O-α-d-mannopyranosyl-α-d-mannopyranoside, methyl 6-O-α-d-galactopyranosyl-3-O-α-d-mannopyranosyl-α-d-mannopyranoside, and methyl 6-O-α-d-glucopyranosyl-3-O-α-d-mannopyranosyl-α-d-mannopyranoside
✍ Per J. Garegg; Stefan Oscarson; Anna-Karin Tidén 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 437 KB

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-