𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Biological activities of chemically synthesized N-acetylneuraminic acid-(α2→6) -monosaccharide analogs of lipid A

✍ Scribed by Tadayori Shimizu; Toshiyuki Masuzawa; Yasutake Yanagihara; Chikako Shimizu; Kiyoshi Ikeda; Kazuo Achiwa


Book ID
115920724
Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
247 KB
Volume
228
Category
Article
ISSN
0014-5793

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Phase-transfer-catalyzed synthesis of ar
✍ Jörg Rothermel; Hans Faillard 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 884 KB

Glycosidation of N-acetylneuraminic acid by phase-transfer catalysis in chloroform-aqueous alkali gave several known and some new aryl cY-ketosides in a short reaction time and in good yields. The 4-methylumbelliferyl cu-ketoside, the standard substrate for neuraminidase, was prepared in a yield of

Combined chemical-enzymic synthesis of a
✍ Mohammed A. Kashem; Cong Jiang; Andre P. Venot; Gordon R. Alton 📂 Article 📅 1992 🏛 Elsevier Science 🌐 English ⚖ 288 KB

Sialylated and fucosylated lactosaminyl structures such as sialyl Lewis', sialyl dimeric Lewis", and its internally monofucosylated derivative have been proposed as ligands for the E-and the P-selectins'-4. The availability of pure synthetic materials is critical for the evaluation of the binding sp