Progress in the chemistry of glycoconjugates during the last decade reflects the availability of a wide array of methods for stereoselective 0-glycosylation'-3. Carbohydrate segments of biological interest can be coupled through a spacer4 to a soluble protein to yield synthetic antigens, and attachm
β¦ LIBER β¦
2-Azidoethyl glycosides: glycosides potentially useful for the preparation of neoglycoconjugates
β Scribed by Anatoly Ya. Chernyak; Gangavaram V.M. Sharma; Leonid O. Kononov; Palakodety Radha Krishna; Anatoly B. Levinsky; Nikolay K. Kochetkov; Alla V. Rama Rao
- Book ID
- 107726130
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 491 KB
- Volume
- 223
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
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## Abstract Chloroacetylation of alkyl glycopyranosides of Ξ²βDβgalactose, Ξ²βDβglucose and Ξ±βDβmannose as well as of free Dβglucose, Dβgalactose, Dβmannose and Dβxylose, using chloroacetic anhydride as acylating reagent, gave the corresponding fully chloroacetylated pyranose derivatives in excellent