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New Efficient Synthesis of β-Glucosylamines of Mono- and Disaccharides with the Use of Ammonium Carbamate

New Efficient Synthesis of β-Glucosylamines of Mono- and Disaccharides with the Use of Ammonium... 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 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Doklady Chemistry Springer Journals

New Efficient Synthesis of β-Glucosylamines of Mono- and Disaccharides with the Use of Ammonium Carbamate

Doklady Chemistry , Volume 383 (6) – Oct 10, 2004

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References (8)

Publisher
Springer Journals
Copyright
Copyright © 2002 by MAIK “Nauka/Interperiodica”
Subject
Chemistry; Chemistry/Food Science, general; Industrial Chemistry/Chemical Engineering
ISSN
0012-5008
eISSN
1608-3113
DOI
10.1023/A:1015428720733
Publisher site
See Article on Publisher Site

Abstract

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

Journal

Doklady ChemistrySpringer Journals

Published: Oct 10, 2004

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