𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Synthesis of Ligands Related to the Vibrio cholerae O-Specific Antigen. Part 6. Synthesis of the 2-Deoxy Analogue of the Methyl α- Glycoside of the Monosaccharide Repeating Unit of the O-Polysaccharide of Vibrio cholerae O:1.

✍ Scribed by Y. OGAWA; P. LEI; P. KOVAC


Book ID
112029378
Publisher
John Wiley and Sons
Year
2010
Weight
34 KB
Volume
27
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of specifically deoxygenated a
✍ Makoto Gotoh; Pavol Kováč 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 713 KB

Treatment of methyl Ot-D-perosaminide (1) with y-butyrolactone gave the 2'-deoxy analogue of methyl 4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-a-D-mannopyranoside (13), the methyl a-glycoside of the intracatenary monosaccharide repeating unit of the O-polysaccharide of Vibrio cholerae O:1. The an

Synthesis and crystal structure of methy
✍ Ping-sheng Lei; Yuji Ogawa; Judith L. Flippen-Anderson; Pavol Kováĉ 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 636 KB

Methyl 4-azido-4,6-dideoxy-3-O-benzyl-ct-D-mannopyranoside and its analogous 3-O-(4methoxybenzyl) derivative were methylated and the 2-O-methyl derivatives formed were convetted into methyl 4-amino-4,6-dideoxy-2-O-methyl-a-o-mannopyranoside. Reaction of the latter with 3-deoxy-L-glycero-tetronolacto