Produktbild: Glycochemical Synthesis

Glycochemical Synthesis Strategies and Applications

243,99 €

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Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

10.10.2016

Herausgeber

Shang-Cheng Hung + weitere

Verlag

John Wiley & Sons Inc

Seitenzahl

576

Maße (L/B/H)

24,4/15,7/3,3 cm

Gewicht

907 g

Auflage

1. Auflage

Sprache

Englisch

ISBN

978-1-118-29984-5

Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

10.10.2016

Herausgeber

Verlag

John Wiley & Sons Inc

Seitenzahl

576

Maße (L/B/H)

24,4/15,7/3,3 cm

Gewicht

907 g

Auflage

1. Auflage

Sprache

Englisch

ISBN

978-1-118-29984-5

Herstelleradresse

Libri GmbH
Europaallee 1
36244 Bad Hersfeld
DE

Email: [email protected]

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  • Produktbild: Glycochemical Synthesis
  • 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 ¿?-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?-¿thioesters, 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