𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Syntheses of sialic acid analogues with acylamino groups at C-4 (N-acyl regioisomers of sialic acids)

✍ Scribed by Xue-Long Sun; Toshitsugu Kai; Hiroaki Takayanagi; Kimio Furuhata


Book ID
108309645
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
828 KB
Volume
298
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Structural variations ofN-acetylneuramin
✍ Hartmann, Michael ;Zbiral, Erich 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 772 KB

## Abstract 2‐Deoxy‐2‐H~eq~‐__N__‐acetylneuraminic acid (1a) has been shown to be a versatile mimic for sialosyl 2‐α‐glycosides to study the hemagglutinin‐sialic acid interaction. Starting with a 4‐oxo derivative of 2‐deoxy‐2‐H~eq~‐sialic acid, we obtained the 4‐__C__‐methyl~ax~ and 4‐__C__‐methyl~

ChemInform Abstract: Chemoenzymatic Synt
✍ Kiyoshi Ikeda; Fuyuki Kimura; Kimihiko Sano; Yasuo Suzuki; Kazuo Achiwa 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB 👁 2 views

Chemoenzymatic Synthesis of an N-Acetylneuraminic Acid Analogue Having a Carbamoylmethyl Group at C-4 as an Inhibitor of Sialidase from Influenza Virus. -The synthetic strategy for the preparation of the title analogue (XVI) requires the key intermediate (XII) which is synthesized by the Neu5Ac aldo