Screen LibraryCarbohydrate chemistry. Volume 42 /
Volume 42 of Carbohydrate Chemistry demonstrates the interdisciplinary nature of modern carbohydrate research, and benefits any researcher who wishes to learn about the latest developments in the carbohydrate field.
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| Corporate Authors: | |
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| Group Author: | ; ; ; ; ; ; ; ; ; |
| Published: |
Royal Society of Chemistry,
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| Publisher Address: | Cambridge : |
| Publication Dates: | 2017. |
| Literature type: | eBook |
| Language: | English |
| Series: |
Specialist Periodical Reports ;
v. 42 |
| Subjects: | |
| Online Access: |
http://dx.doi.org/10.1039/9781782626657 |
| Summary: |
Volume 42 of Carbohydrate Chemistry demonstrates the interdisciplinary nature of modern carbohydrate research, and benefits any researcher who wishes to learn about the latest developments in the carbohydrate field. |
| Carrier Form: | 1 online resource (382 pages). |
| ISBN: |
9781782626657 1782626654 |
| Index Number: | QD321 |
| CLC: | O629.1 |
| Contents: |
Cover; Contents; Preface; Contemporary glycoconjugation chemistry; 1 Introduction; 2 Established chemical methodologies; 3 Newer chemical methodologies; 4 Newer enzymatic methodologies; 5 Conclusions and future perspective; Acknowledgments; References; Recent advances in the application of NMR methods to uncover the conformation and recognition features of glycans; 1 Introduction; 2 Mono-, oligo- and poly-saccharides. Conformation and dynamics in solution; 3 The bound state; 4 Oligosaccharide-protein interactions: lectins; 5 Oligosaccharide-protein interactions: antibodies. 6 Oligosaccharide-protein interactions: enzymes7 Polysaccharide interactions; 8 Glycopeptides. The free state; 9 Glycopeptide-antibody interactions; 10 Glycopeptide-lectin interactions; 11 Glycomimetics: structural and conformational features; 12 Glycomimetic interactions: lectins and enzymes; 13 Other interactions. Artificial receptors for carbohydrates; 14 Cyclodextrins; 15 Carbohydrate-nucleic acid interactions; 16 Concluding remarks; Acknowledgments; References; Controlled and highly efficient preparation of carbohydrate-based vaccines: squaric acid chemistry is the way to go. 1 Introduction2 The early days; 3 More recent conjugations of synthetic oligosaccharides; 4 Conjugation of bacterial polysaccharides; 5 The road to the present state of the art; 6 Practical considerations; 7 Suggested conjugation protocols; Acknowledgments; References; Recent advances in Kdo-glycoside formation; 1 Introduction; 2 Chemistry of Kdo glycoside formation; 3 Conclusions and outlook; Abbreviations; Acknowledgments; References; Chemical and enzymatic approaches to the synthesis of cyclic oligosaccharides; 1 Introduction; 2 Cyclic oligosaccharides retained with glycosidic oxygen. 3 Linear oligosaccharides formed through glycosidic bond cleavage of native CDs and subsequent cyclization to cyclic oligosaccharides4 Polycondensation of designed oligosaccharide monomers; 5 Enzymatic methods to prepare cyclic oligosaccharides; 6 Conclusion; Abbreviations; Acknowledgments; References; Ferrier rearrangement: an update on recent developments; 1 Introduction; 2 Pd-catalyzed Ferrier rearrangement; 3 Lewis-acid catalyzed Ferrier rearrangement; 4 Ferrier rearrangement mediated by acids; 5 Oxidative promoters; 6 Miscellaneous activation protocols. 7 Miscellaneous transformations of glycals8 Ferrier rearrangement on C-1 or C-2 substituted glycal systems; 9 Polarity inversion in the Ferrier rearrangement; 10 Conclusion; Acknowledgments; References; FimH antagonists -- solubility vs. permeability; 1 Introduction; 2 Results and discussion; 3 Conclusions; Abbreviations; Acknowledgments; References; Carbohydrate steroid hybrid architectures: the viewpoint of amphiphilicity and self-organisation; 1 Introduction; 2 The different classes of glycosteroids, classified by molecular shape. 3 Investigations on supramolecular systems made of glycosteroids. |