
Carbohydrate Chemistry
Volume 36
Royal Society of Chemistry (Publisher)
Published on 19. July 2010
Book
Hardback
208 pages
978-1-84755-044-6 (ISBN)
Description
Carbohydrate Chemistry provides review coverage of all publications relevant to the chemistry of monosaccharides and oligosaccharides in a given year. The amount of research in this field appearing in the organic chemical literature is increasing because of the enhanced importance of the subject, especially in areas of medicinal chemistry and biology. In no part of the field is this more apparent than in the synthesis of oligosaccharides required by scientists working in glycobiology. Clycomedicinal chemistry and its reliance on carbohydrate synthesis is now very well established, for example, by the preparation of specific carbohydrate- based antigens, especially cancer-specific oligosaccharides and glycoconjugates. Coverage of topics such as nucleosides, amino-sugars, alditols and cyclitols also covers much research of relevance to biological and medicinal chemistry. Each volume of the series brings together references to all published work in given areas of the subject and serves as a comprehensive database for the active research chemist Specialist Periodical Reports provide systematic and detailed review coverage in major areas of chemical research. Compiled by teams of leading authorities in the relevant subject areas, the series creates a unique service for the active research chemist, with regular, in-depth accounts of progress in particular fields of chemistry. Subject coverage within different volumes of a given title is similar and publication is on an annual or biennial basis.
More details
Series
Language
English
Place of publication
Cambridge
United Kingdom
Target group
Professional and scholarly
Product notice
Unsewn / adhesive bound
Dimensions
Height: 234 mm
Width: 156 mm
Thickness: 13 mm
Weight
465 gr
ISBN-13
978-1-84755-044-6 (9781847550446)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions

E-Book
08/2010
1st Edition
Royal Society of Chemistry
€413.99
Available for download
Persons
Amelia Pilar Rauter is Head of Carbohydrate Chemistry Group in the Chemistry and Biochemistry department of the University of Lisbon, Portugal. Thisbe K Lindhorst is Professor of Organic and Bioorganic Chemistry at the University of Kiel, Germany.
Editor
Universidade de Lisboa, Portugal
Kiel University, Germany
Content
1. Synthetic Vaccines Based on N- and O-Glycopeptidesu Molecular Tools for Immunotherapy and Diagnostics;
2. Mycobacterial Lipoarabinomannan Fragments as Haptens for Potential Anti-Tuberculosis Vaccines;
3. a-Galactosylceramides and Analogues as Important Immunomodulators for Use as vaccine Adjuvants;
4. Synthetic Glycoconjugates Based on Leishmania Lipophosphoglycan Structures as Potential Anti-Leishmaniasis Vaccines;
5. Solution- and Solid-Phase Synthesis of Oligosaccharides 6. Advances in Chemoenzymatic Synthesis of Glycopeptides for Cancer Research Applications 7. Bioorthogonal Chemical Reporter Methodology for Visualization, Isolation and Analysis of Glycoconjugates 8. Azido Leaving Group in Enzymatic Synthesis - Small and Efficient 9. Recent Advances in the Synthesis of Functionalized Carbohydrate Azides
2. Mycobacterial Lipoarabinomannan Fragments as Haptens for Potential Anti-Tuberculosis Vaccines;
3. a-Galactosylceramides and Analogues as Important Immunomodulators for Use as vaccine Adjuvants;
4. Synthetic Glycoconjugates Based on Leishmania Lipophosphoglycan Structures as Potential Anti-Leishmaniasis Vaccines;
5. Solution- and Solid-Phase Synthesis of Oligosaccharides 6. Advances in Chemoenzymatic Synthesis of Glycopeptides for Cancer Research Applications 7. Bioorthogonal Chemical Reporter Methodology for Visualization, Isolation and Analysis of Glycoconjugates 8. Azido Leaving Group in Enzymatic Synthesis - Small and Efficient 9. Recent Advances in the Synthesis of Functionalized Carbohydrate Azides