Glycochemical Synthesis
John Wiley & Sons Inc (Verlag)
978-1-118-29984-5 (ISBN)
This book is a comprehensive and concise review on principles, strategies, and crucial advances in glycochemistry. It focuses on synthesis and practical applications and emphasizes state-of-the-art approaches to the assembly and design of sugars.
• Provides detailed discussion on specific topics like oligosaccharide assembly and design of sugars, techniques in glycoconjugate preparation, multivalency, and carbohydrate-based drug design
• Uses notable examples, like solution-based one-pot methods and automated methods for sugar assembly, to illustrate important concepts and advances in a rapidly emerging field
• Discusses practical applications of carbohydrates, like medicine, therapeutics, drug and vaccine development
Shang-Cheng Hung, PhD, is a Distinguished Research Fellow of the Genomics Research Center, Academia Sinica, Taiwan. His work focuses on carbohydrate chemistry and chemical biology, including the development of novel approaches to glycan synthesis and the acquisition of important cell-surface glycan components together with their biological evaluations. Medel Manuel L. Zulueta, PhD, is a carbohydrate chemist at the Genomics Research Center, Academia Sinica, Taiwan. He develops of strategies for the chemical synthesis of oligosaccharides, particularly heparin and heparan sulfate.
Contributors xv
Foreword xix
Preface xxiii
1 Glycochemistry: Overview and Progress 1
Matthew Schombs and Jacquelyn Gervay-Hague
1.1 Introduction, 1
1.2 Nomenclature, Structures, and Properties of Sugars, 2
1.3 Historical Overview of Carbohydrate Research, 12
1.4 Onward to the Twenty-First Century, 22
1.5 Conclusion and Outlook, 28
References, 29
2 Protecting Group Strategies in Carbohydrate Synthesis 35
Shang-Cheng Hung and Cheng-Chung Wang
2.1 Introduction, 35
2.2 General Considerations for Protecting Group Selection, 36
2.3 Common Protecting Groups in Carbohydrate Synthesis, 38
2.4 Regioselective Protection of Monosaccharides, 46
2.5 One-Pot Protection Methods, 57
2.6 Conclusion, 61
References, 62
3 General Aspects in O-Glycosidic Bond Formation 69
Xin-Shan Ye and Weigang Lu
3.1 Introduction, 69
3.2 Some Basic Concepts, 69
3.3 Methods for Glycosidic Bond Formation, 74
3.4 Glycosylation Strategies, 86
3.5 Conclusion, 91
References, 91
4 Controlling Anomeric Selectivity, Reactivity, and Regioselectivity in Glycosylations Using Protecting Groups 97
Thomas Jan Boltje, Lin Liu, and Geert-Jan Boons
4.1 Introduction, 97
4.2 Protecting Group and Control of Anomeric Selectivity of Glycosylations, 98
4.3 Use of Protecting Groups for Chemoselective Glycosylations, 115
4.4 Protecting Groups in Regioselective Glycosylations, 118
4.5 Conclusion, 125
References, 125
5 Stereocontrolled Synthesis of Sialosides 131
Chandrasekhar Navuluri and David Crich
5.1 Introduction, 131
5.2 Conformational Analysis of Sialyl Oxocarbenium Ions, 132
5.3 Additives in Sialylations, 133
5.4 Leaving Groups in Sialylations, 134
5.5 Influence of the N5 Protecting Group on Reactivity and Selectivity, 134
5.6 4-O,5-N-Oxazolidinone Group and its Stereodirecting Influence on Sialylations, 139
5.7 4,5-O-Carbonate Protecting Group in α-Selective KDN Donors, 144
5.8 Other Cyclic and Bicyclic Protecting Systems for Sialyl Donors, 145
5.9 Mechanistic Aspects of Sialylation with Cyclically Protected Sialyl Donors, 146
5.10 Influence of Hydroxy Protecting Groups on Sialyl Donor Reactivity and Selectivity, 147
5.11 Stereoselective C-Sialoside Formation, 148
5.12 Stereoselective S-Sialoside Formation, 149
5.13 Conclusion, 151
References, 151
6 Strategies for One-Pot Synthesis of Oligosaccharides 155
Bo Yang, Keisuke Yoshida, and Xuefei Huang
6.1 Introduction, 155
6.2 One-Pot Glycosylation from the Nonreducing End to the Reducing End, 156
6.3 Regioselective One-Pot Glycosylation: Construction of Oligosaccharides from the Reducing End to the Nonreducing End, 175
6.4 Hybrid One-Pot Glycosylation, 179
6.5 Conclusion, 183
Acknowledgments, 183
References, 183
7 Automated Oligosaccharide Synthesis: Techniques and Applications 189
Mattan Hurevich, Jeyakumar Kandasamy, and Peter H. Seeberger
7.1 Introduction, 189
7.2 Challenges and Limitations in Solution-Phase Oligosaccharide Synthesis, 190
7.3 Solid-Phase Oligosaccharide Synthesis, 191
7.4 Automated Oligosaccharide Synthesis, 193
7.5 Microfluidic Techniques for Oligosaccharide Synthesis, 199
7.6 Conclusion and Outlook, 202
Acknowledgments, 202
References, 202
8 Sugar Synthesis by Microfluidic Techniques 205
Koichi Fukase, Katsunori Tanaka, Yukari Fujimoto, Atsushi Shimoyama, and Yoshiyuki Manabe
8.1 Introduction, 205
8.2 Microfluidic Glycosylation, 206
8.3 Conclusion, 216
References, 217
9 Chemoenzymatic Synthesis of Carbohydrates 221
Kasemsiri Chandarajoti and Jian Liu
9.1 Introduction, 221
9.2 Oligosaccharides and Polysaccharides Produced by GTases, 222
9.3 Chemoenzymatic Synthesis of HS, 223
9.4 Conclusion, 231
References, 231
10 Synthesis of Glycosaminoglycans 235
Medel Manuel L. Zulueta, Shu-Yi Lin, Yu-Peng Hu, and Shang-Cheng Hung
10.1 Introduction, 235
10.2 General Strategies, 238
10.3 Synthesis of Derivatives of l-Idose and IdoA, 240
10.4 Synthesis via Stepwise Solution-Phase Assembly and Compound Diversification, 242
10.5 Synthesis via Solution-Phase One-Pot Assembly, 250
10.6 Polymer-Supported Synthesis and Automation, 253
10.7 GAG Mimetics, 256
10.8 Conclusion, 257
References, 258
11 Chemical Glycoprotein Synthesis 263
Yasuhiro Kajihara, Masumi Murakami, and Carlo Unverzagt
11.1 Introduction, 263
11.2 Oligosaccharide Structures, 264
11.3 Biosynthesis of Glycoproteins, 265
11.4 Chemical Protein Synthesis, 267
11.5 Synthesis of Glycopeptides, 269
11.6 Synthesis of Glycopeptide-αthioesters, 270
11.7 Chemical Synthesis of Glycoproteins, 275
11.8 Conclusion, 288
References, 288
12 Synthesis of Glycosphingolipids 293
Suvarn S. Kulkarni
12.1 Introduction, 293
12.2 Classification and Nomenclature of GSLs, 294
12.3 Biological Significance of GSLs, 296
12.4 Synthesis of GSLs, 297
12.5 Conclusion, 320
References, 320
13 Synthesis of Glycosylphosphatidylinositol Anchors 327
Charles Johnson and Zhongwu Guo
13.1 Introduction, 327
13.2 Synthesis of the Tryp. brucei GPI Anchor, 328
13.3 Synthesis of the Yeast GPI Anchor, 333
13.4 Synthesis of the Rat Brain Thy-1 GPI Anchor, 335
13.5 Synthesis of Plasmodium falciparum GPI Anchor, 340
13.6 Synthesis of Trypanosoma cruzi GPI Anchor, 344
13.7 Synthesis of a Human Sperm CD52 Antigen GPI Anchor, 349
13.8 Synthesis of a Human Lymphocyte CD52 Antigen GPI Anchor, 351
13.9 Synthesis of the Branched GPI Anchor of Toxoplasma gondii, 354
13.10 Conclusion, 355
Acknowledgment, 356
References, 357
14 Synthesis of Bacterial Cell Envelope Components 361
Akihiro Ishiwata and Yukishige Ito
14.1 Introduction, 361
14.2 Peptidoglycan and Related Glycoconjugates, 362
14.3 LPS and Related Glycoconjugates, 371
14.4 Lipoteichoic Acid, 380
14.5 Mycolyl Arabinogalactan, LAM, and Related Glycoconjugates, 382
14.6 Oligosaccharides of Bacterial Glycoprotein and Related Glycoconjugates, 390
14.7 Conclusion, 394
References, 395
15 Discoveries and Applications of Glycan Arrays 407
Chung-Yi Wu and Shih-Huang Chang
15.1 Introduction, 407
15.2 Discoveries of Glycan Arrays, 407
15.3 Applications of Glycan Array, 412
15.4 Conclusion, 418
References, 418
16 Synthesis and Applications of Glyconanoparticles, Glycodendrimers, and Glycoclusters in Biological Systems 425
Avijit Kumar Adak, Ching-Ching Yu, and Chun-Cheng Lin
16.1 Introduction, 425
16.2 Significance of Multivalent Binding Interactions in Biological Systems, 426
16.3 Glyconanoparticles, Glycodendrimers, and Glycoclusters: General Overview, 428
16.4 Plant Lectins, 431
16.5 AB5 Toxins, 438
16.6 Bacterial Adhesion Lectins, 440
16.7 Influenza Virus, 445
16.8 Detection of Bacteria, 445
16.9 Glyco-MNPs as Nanoprobes for Labeling Cells and Magnetic Resonance Imaging Agents, 446
16.10 Cyclopeptide-Based Glycoclusters as Vaccine Adjuvants, 447
16.11 Conclusion, 449
Acknowledgments, 449
References, 450
17 Design and Synthesis of Carbohydrates and Carbohydrate Mimetics as Anti-Influenza Agents 455
Mauro Pascolutti and Mark von Itzstein
17.1 Introduction, 455
17.2 Influenza Viruses, 456
17.3 Development of Anti-Influenza Therapeutics, 459
17.4 Sialic Acid: The Viral Cell-Surface Receptor Ligand, 460
17.5 Hemagglutinin, 460
17.6 Sialidase, 461
17.7 Influenza Virus Sialidase as a Drug Discovery Target, 464
17.8 Structural Differences Recently Identified in Influenza a Virus Sialidase Subtypes, 471
17.9 New Influenza Virus Sialidase Inhibitors Targeting the 150-Cavity, 473
References, 476
18 Design and Synthesis of Ligands and Antagonists of Siglecs as Immune Response Modifiers 483
Hajjaj H. M. Abdu-Allah, Hideharu Ishida, and Makoto Kiso
18.1 Introduction, 483
18.2 Lectins, 484
18.3 Siglecs, 484
18.4 Siglecs and Innate Immunity, 489
18.5 Design and Synthesis of High-Affinity Ligands for Siglecs, 494
18.6 Conclusion and Future Directions, 501
References, 502
19 Sugar–Protein Hybrids for Biomedical Applications 509
Macarena Sánchez-Navarro and Benjamin G. Davis
19.1 Introduction, 509
19.2 Challenges in the Development of Glycoprotein-Based Therapeutics, 510
19.3 Why Unnatural? 510
19.4 Retrosynthetic Analysis, 511
19.5 Linkages, 512
19.6 Glycoprotein-Based Therapeutics, 521
19.7 Conclusion, 527
References, 527
Index 535
| Erscheint lt. Verlag | 28.10.2016 |
|---|---|
| Verlagsort | New York |
| Sprache | englisch |
| Maße | 158 x 236 mm |
| Gewicht | 885 g |
| Themenwelt | Naturwissenschaften ► Biologie ► Biochemie |
| Naturwissenschaften ► Chemie ► Organische Chemie | |
| Naturwissenschaften ► Chemie ► Physikalische Chemie | |
| Technik ► Maschinenbau | |
| ISBN-10 | 1-118-29984-1 / 1118299841 |
| ISBN-13 | 978-1-118-29984-5 / 9781118299845 |
| Zustand | Neuware |
| Haben Sie eine Frage zum Produkt? |
aus dem Bereich
