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Synthesis of a Useful Lauryl Thioglycoside of Sialic Acid and Its Application.

โœ Scribed by Koji Matsuoka; Tomotsune Onaga; Tomonori Mori; Jun-Ichi Sakamoto; Tetsuo Koyama; Nobuo Sakairi; Ken Hatano; Daiyo Terunuma


Book ID
101972389
Publisher
John Wiley and Sons
Year
2005
Weight
31 KB
Volume
36
Category
Article
ISSN
0931-7597

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โœฆ Synopsis


Abstract

For Abstract see ChemInform Abstract in Full Text.


๐Ÿ“œ SIMILAR VOLUMES


An azidoaryl thioglycoside of sialic aci
โœ Thomas G. Warner; Laura A. Lee ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 571 KB

An azidoaryl thioglycoside of sialic acid was prepared, as a potential photoaffinity probe reagent for the analysis of sialidases and sialic acid-binding proteins, by treatment of the glycosyl chloride of N-acetylneuraminic acid methyl ester with potassium thioacetate to give, in 70% yield, methyl 5

Synthesis of a useful anomeric thioaceta
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A novel anomeric b-thioacetate of an N-acetyllactosamine derivative was efficiently synthesized in high yield from the known 2-azido glycosyl chloride using thioacetic acid as a convenient reagent. The synthesis involved not only an S N 2 replacement of the chloride by a carbothiolate anion but also