Website to accompany Essentials of Carbohydrate Chemistry and Biochemistry
Website to accompany Essentials of Carbohydrate Chemistry and Biochemistry
From synthesis to biological function, "Essentials of Carbohydrate Chemistry and Biochemistry" introduces the entire range of modern carbohydrate chemistry and chemical biology. In this new edition, the increasing recognition of the role of carbohydrates in biology, pharmacology, and medicine is reflected in greatly expanded sections on glycobiology and glycomimetics. The new edition also features a new set of illustrations, many of which are now in color, as well as intriguing practical examples and story-telling text boxes providing context for the relevance of carbohydrates in science and society.
Didactically written by an experienced lecturer and graduate student advisor, "Essentials of Carbohydrate Chemistry and Biochemistry" includes information on:
- Protecting groups for carbohydrates, including protection of the anomeric center, acyl, ether, and acetal protecting groups
- Methods for the analysis of carbohydrates, covering polarimetry, NMR spectroscopy, and mass spectrometry
- Important modifications and functionalizations of the sugar ring, such as deoxy derivatives, anhydro sugars, and epimerizations
- Principal approaches to the chemical and enzymatic synthesis of glycosides and glycopeptides, and modern examples of advancing the art of glycoside synthesis employing solution as well as solid phase methods
- Structural diversity and biosynthesis of oligosaccharides and glycoconjugates
- A greatly expanded section on glycobiology that focuses on the role of carbohydrates in membrane architecture, cell-cell-recognition. cell adhesion, and their biomedical applications.
Updated and thoroughly modernized for more efficient classroom teaching and self-learning, the Fourth Edition of "Essentials of Carbohydrate Chemistry and Biochemistry" is essential reading for students in chemistry, biochemistry, biotechnology, and pharmacy with an interest in glycochemistry and glycobiology.
1 Structure of saccharides
Didactically written by an experienced lecturer and graduate student advisor, "Essentials of Carbohydrate Chemistry and Biochemistry" includes information on:
- Protecting groups for carbohydrates, including protection of the anomeric center, acyl, ether, and acetal protecting groups
- Methods for the analysis of carbohydrates, covering polarimetry, NMR spectroscopy, and mass spectrometry
- Important modifications and functionalizations of the sugar ring, such as deoxy derivatives, anhydro sugars, and epimerizations
- Principal approaches to the chemical and enzymatic synthesis of glycosides and glycopeptides, and modern examples of advancing the art of glycoside synthesis employing solution as well as solid phase methods
- Structural diversity and biosynthesis of oligosaccharides and glycoconjugates
- A greatly expanded section on glycobiology that focuses on the role of carbohydrates in membrane architecture, cell-cell-recognition. cell adhesion, and their biomedical applications.
Updated and thoroughly modernized for more efficient classroom teaching and self-learning, the Fourth Edition of "Essentials of Carbohydrate Chemistry and Biochemistry" is essential reading for students in chemistry, biochemistry, biotechnology, and pharmacy with an interest in glycochemistry and glycobiology.
1 Structure of saccharides
1.1 Structure of monosaccharides
1.2 Structure of oligosaccharides
1.3 Structure of polysaccharides
1.4 Nomenclature of saccharides
References and key terms
2 Protecting groups for carbohydrates
2.1 Acyl protecting groups
2.2 Ether protecting groups
2.3 Selective protection of the primary hydroxyl group
2.4 Cyclic protecting groups
2.5 Orthoesters as protecting groups
2.6 Protection of the anomeric centre
2.7. One catalyst-one pot protections of per-silylated sugars
2.8 N-Protection for amino sugars
2.9 Enzymes in protecting group chemistry
2.10 Strategic protecting-group sequences on carbohydrate scaffolds
References and key terms
3 O-Glycoside synthesis
3.1 1,2-trans and 1,2-cis Glycosidation
3.2 Factors that influence a glycosylation reaction
3.3 The Koenigs-Knorr method
3.4 Glycosyl acetimidates
3.5 Thioglycosides
3.6 n-Pentenyl glycosides
3.7. Gold?catalysed glycoside synthesis
3.8 Synthesis of 2-deoxy glycosides
3.9 Synthesis of alpha-D-glucosides and beta-D-mannosides
3.10 Synthesis of 2-acetamido-2-deoxy glycosides
3.11 Solid phase oligosaccharide synthesis
3.12 Glycoside synthesis employing enzymes
3.13 Glycosylation strategies
References and key terms
4 Important modifications of the sugar ring
4.1 Activation?substitution reactions at the carbohydrate ring: Deoxyhalo derivatives
4.2 Deoxygenation of carbohydrates
4.3 Epimerisations
4.4 From azido to amino and more: N-functionalised sugars
4.5 Important unsaturated saccharides
4.6 Unexpected journeys of sugars
References and key terms
5 Structure and biosynthesis of glycoconjugates
5.1 Size, diversity, and representation
5.1.1 The actual size of carbohydrates
5.1.2 Structural diversity of oligosaccharides
5.1.3 The symbol representation of carbohydrates
5.2 Structures of glycoconjugates
5.3 Biosynthesis of oligosaccharides
5.3.1 Biosynthesis of N-glycoproteins
5.3.2 Biosynthesis of O-glycoproteins
5.3.3 Biosynthesis of glycosphingolipids
References and key terms
6 Glycobiology
6.1 The glycocalyx
6.2 The lectins
6.3 Carbohydrate microarrays
6.4 Glycomimetics and carbohydrate drugs
6.5 Microbial adhesion - FimH antagonists and catch bonds
6.6 The clinical impact of glycobiology
6.8 Glycan atlassing
References and key terms
| ISBN | 9783527350636 |
|---|---|
| Medientyp | Buch |
| Auflage | 4. Aufl. |
| Copyrightjahr | 2026 |
| Verlag | Wiley-VCH GmbH Wiley-VCH GmbH, Boschstrasse 12, DE-69469 Weinheim |
| Umfang | 352 Seiten |
| Abbildungen | 257 SW-Abb., 50 Farbabb. |
| Sprache | Englisch |