Access the full text.
Sign up today, get DeepDyve free for 14 days.
R. Tipson (1961)
Acetylation of D-Ribosylamine1Journal of Organic Chemistry, 26
A. Lubineau, J. Augé, B. Drouillat (1995)
Improved synthesis of glycosylamines and a straightforward preparation of N-acylglycosylamines as carbohydrate-based detergents.Carbohydrate research, 266 2
L. Urge, L. Otvos, E. Lång, K. Wroblewski, I. Laczkó, M. Hollósi (1992)
Fmoc-protected, glycosylated asparagines potentially useful as reagents in the solid-phase synthesis of N-glycopeptides.Carbohydrate research, 235
R. Whistler, M. Wolfrom, J. BeMiller, D. Shaw (1965)
Methods in Carbohydrate Chemistry
F. Micheel, R. Frier, E. Plate, A. Hiller (1952)
Neue Darstellungsmethoden für 1‐Amino‐Zucker und einige ihrer N‐SubstitutionsprodukteChemische Berichte, 85
I. Manger, T. Rademacher, R. Dwek (1992)
1-N-glycyl beta-oligosaccharide derivatives as stable intermediates for the formation of glycoconjugate probes.Biochemistry, 31 44
H. Isbell, H. Frush (1958)
Mutarotation, Hydrolysis, and Rearrangement Reactions of Glycosylamines1Journal of Organic Chemistry, 23
Michel Monsigny, C. Quétard, Sylvain Bourgerie, Didier Delay, Chantal Pichon, P. Midoux, Roger Mayer, A. Roche (1998)
Glycotargeting: the preparation of glyco-amino acids and derivatives from unprotected reducing sugars.Biochimie, 80 2
Doklady Chemistry, Vol. 383, Nos. 4–6, 2002, pp. 89–92. Translated from Doklady Akademii Nauk, Vol. 383, No. 4, 2002, pp. 500–503. Original Russian Text Copyright © 2002 by Likhosherstov, Novikova, Shibaev. CHEMISTRY New Efficient Synthesis of b-Glucosylamines of Mono- and Disaccharides with the Use of Ammonium Carbamate L. M. Likhosherstov, O. S. Novikova, and V. N. Shibaev Presented by Academician N. K. Kochetkov January 8, 2002 Received January 9, 2002 In recent years, strategies to synthesize different amounts of the volatile salt restricts, however, the appli- neoglucoconjugates used for studying the specificity of cation of the method in preparative syntheses. More- over, glucosylamines are unstable in aqueous solutions biological interactions with the participation of carbo- hydrate residues and for targeted transport of different and undergo fast hydrolysis at pH 1.5 to 9.0 and pro- pharmaceuticals in organisms have been extensively duce diglucosylamines in concentrated solutions. The developed. Glucosylamines of mono- and oligosaccha- rate of these reactions, which occur upon the isolation rides are promising starting compounds for the synthe- of glucosylamines, depends considerably on the nature of the sugar used, which strongly affects the yield and sis of similar compounds. However, the available meth- ods for the synthesis of
Doklady Chemistry – Springer Journals
Published: Oct 10, 2004
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.