Timely Research Perspectives in Carbohydrate Chemistry

2002
ISBN: 978-3-211-83777-1
Verlag: Springer Vienna

Buch, Englisch, 256 Seiten, HC runder Rücken kaschiert, Format (B × H): 215 mm x 285 mm, Gewicht: 915 g

This book includes a collection of minireviews and research papers written by international leaders in the field of carbohydrate chemistry as well as promising young talents. The contents of the contributions span from natural products over structure elucidation with special emphasis on spectroscopy, syntheses and synthetic methods, biological activities, applications of carbohydrates and carbohydrate mimetics as well as their use as molecular scaffolds and carriers of biological information.
The reader will get a representative overview of state-of-the-art research topics and approaches.

Zielgruppe

Research

Autoren/Hrsg.

Stütz, Arnold E.

Schmid, Walther

Fachgebiete

• Naturwissenschaften Biowissenschaften Kohlenhydrate
• Naturwissenschaften Biowissenschaften Biochemie (nichtmedizinisch)
• Technische Wissenschaften Verfahrenstechnik | Chemieingenieurwesen | Biotechnologie Lebensmitteltechnologie und Getränketechnologie
• Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Klinische und Innere Medizin Immunologie
• Naturwissenschaften Chemie Organische Chemie Biochemie

Inhaltsverzeichnis

Invited Reviews: Lipases as Useful Tools for the Stereo- and Regioselective Protection and Deprotection of Carbohydrates (La Ferla B.); Carbohydrate-Based Scaffolds for the Generation of Sortiments of Bioactive Compounds (Peri F., Cipolla L., Forni E., Nicotra F.); Conversions of Nitroalkyl to Carbonyl Groups in Carbohydrates (Petruš L., Petrušová M., Pham-Huu D.-P., Lattová E., Pribulová B., Turjan, J.); From Lianas to Glycobiology Tools: Twenty-five Years of 2,5-Dideoxy-2,5-imino-D-mannitol (Wrodnigg T. M.).- Contributions: Rearrangements in the Course of Fluorination by Diethylaminosulfur Trifluoride at C-2 of Glycopyranosides: Some New Parameters (Dax K., Albert M., Hammond D., Illaszewicz C., Purkarthofer T., Tscherner M., Weber H.); Allyl Protecting Group Mediated Intramolecular Aglycon Delivery (IAD) of Glycosyl Fluorides (Cumpstey I., Fairbanks A. J., Redgrave A. J.); Zinc-Mediated Fragmentation of Methyl 6-Deoxy-6-iodo-hexopyranosides (Skaanderup P. R., Hyldtoft L., Madsen R.); Reactivity Tournament of Isothiocyanato-Functionalized Saccharides with 1,6-Diamino-3,6-oxaoctane (Walter M., Lindhorst T. K.); Photochemical Transformation of Levoglucosan Imides to Anhydrosugar-Annelated Azepanediones and Azocanediones (Sund C., Thiering S., Thiem J., Kopf J., Stark M.); Synthesis and Biological Activity of a Series of Methylene-Expanded Oxetanocin Nucleoside Analogues (Jung M. E., Toyota A., de Clercq E., Balzarini J.); Thiosugars VI: A Simple Stereoselective Approach to (1®3)-3-S-Thiodisaccharides from Levoglucosenone (Witczak Z. J., Kaplon P., Kolodziej M.); Synthesis of Sulfur-Containing Analogues of aGalNAc (Tn-Antigen) and bGal1,3aGalNAc (T-Antigen) (Wenzl I., Neuwirth N., Hedenetz A. G., Fiedler C., Streicher H., Unger F. M., Schmid W.); The Chameleon of Retaining Glycoside Hydrolases and Retaining Glycosyl Transferases: The Catalytic Nucleophile (Stick R. V., Watts A. G.); N-Alkylated Derivatives of 1,5-Dideoxy-1,5-iminoxylitol as b-Xylosidase andb-Glucosidase Inhibitors (Häusler H., Rupitz K. Stütz A. E., Withers S. G.); Synthesis of C-8 Deuterated Glycosides of 3-Deoxy-D-manno-oct-2-ulosonic Acid (Kdo) Related to Chlamydial Lipopolysaccharides (Kosma P., Strobl M., Hofinger A., Duus J. Ø., Petersen B. O., Bock K., Brade H.); Carbohydrate Auxiliaries in Stereoselective Syntheses of Decahydroquinoline Alkaloids (Weymann M., Schulz-Kukula M., Knauer S., Kunz H.); Analysis of Carbohydrate Mixtures by Diffusion Difference NMR Spectroscopy (Kählig H., Dietrich K., Dorner S.)