LEADER 05460nam 2200673Ia 450 001 9910830267903321 005 20170810194931.0 010 $a1-282-47206-2 010 $a9786612472060 010 $a0-470-74886-9 010 $a0-470-74885-0 035 $a(CKB)2550000000002112 035 $a(EBL)477884 035 $a(OCoLC)463438682 035 $a(SSID)ssj0000335873 035 $a(PQKBManifestationID)11273401 035 $a(PQKBTitleCode)TC0000335873 035 $a(PQKBWorkID)10278286 035 $a(PQKB)10546062 035 $a(MiAaPQ)EBC477884 035 $a(PPN)143478532 035 $a(EXLCZ)992550000000002112 100 $a20090428d2009 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aClick chemistry for biotechnology and materials science$b[electronic resource] /$fedited by Joerg Lahann 210 $aChichester, West Sussex $cWiley$d2009 215 $a1 online resource (433 p.) 300 $aDescription based upon print version of record. 311 $a0-470-69970-1 320 $aIncludes bibliographical references and index. 327 $aClick Chemistry for Biotechnologyand Materials Science; Contents; Preface; List of Contributors; Acknowledgments; 1 Click Chemistry: A Universal Ligation Strategy for Biotechnology and Materials Science; 1.1 Introduction; 1.2 Selected Examples of Click Reactions in Materials Science and Biotechnology; 1.3 Potential Limitations of Click Chemistry; 1.4 Conclusions; References; 2 Common Synthons for Click Chemistry in Biotechnology; 2.1 Introduction - Click Chemistry; 2.2 Peptides and Derivatives; 2.3 Peptoids; 2.4 Peptidic Dendrimers; 2.5 Oligonucleotides; 2.6 Carbohydrates; 2.7 Conclusion 327 $aReferences3 Copper-free Click Chemistry; 3.1 Introduction; 3.2 Bio-orthogonal Ligations; 3.2.1 Condensations of Ketones and Aldehydes with Heteroatom-bound Amines; 3.2.2 Staudinger Ligation of Phosphines and Azides; 3.2.3 Copper-free Azide-Alkyne Cycloadditions; 3.2.4 Bioorthogonal Ligations of Alkenes; 3.3 Applications of Copper-free Click Chemistries; 3.3.1 Activity-based Profiling of Enzymes; 3.3.2 Site-specific Labeling of Proteins; 3.3.3 Metabolic Labeling of Glycans; 3.3.4 Metabolic Targeting of Other Biomolecules with Chemical Reporters; 3.4 Summary and Outlook; References 327 $a4 Protein and Peptide Conjugation to Polymers and Surfaces Using Oxime Chemistry4.1 Introduction; 4.2 Protein/Peptide-Polymer Conjugates; 4.3 Immobilization of Proteins and Peptides on Surfaces; 4.4 Conclusions; References; 5 The Role of Click Chemistry in Polymer Synthesis; 5.1 Introduction; 5.2 Polymerization via CuAAC; 5.3 Post-polymerization Modification via Click Chemistry; 5.4 Polymer-Biomacromolecule Conjugation; 5.5 Functional Nanomaterials; 5.6 Summary and Outlook; References; 6 Blocks, Stars and Combs: Complex Macromolecular Architecture Polymers via Click Chemistry 327 $a6.1 Introduction6.2 Block Copolymers; 6.2.1 Preparing Polymers for Click Conjugations; 6.2.2 The Click Reaction: Methodologies and Isolation; 6.2.3 Polymer Characterization; 6.3 Star Polymers; 6.3.1 Star polymers An; 6.3.2 Dentritic Star Polymers; 6.4 Graft Copolymers; 6.4.1 'Grafting-to' Azide Main Chains; 6.4.2 'Grafting-to' Alkyne Main Chains; 6.4.3 Non-CuAAC Routes; 6.5 Concluding Remarks; References; 7 Click Chemistry on Supramolecular Materials; 7.1 Introduction; 7.2 Click Reactions on Rotaxanes, Cyclodextrines and Macrocycles; 7.2.1 Click with Rotaxanes; 7.2.2 Click on Cyclodextrines 327 $a7.2.3 Click on Macrocycles7.3 Click Reactions on DNA; 7.4 Click Reactions on Supramolecular Polymers; 7.5 Click Reactions on Membranes; 7.6 Click Reactions on Dendrimers; 7.7 Click Reactions on Gels and Networks; 7.8 Click Reactions on Self-assembled Monolayers; References; 8 Dendrimer Synthesis and Functionalization by Click Chemistry for Biomedical Applications; 8.1 Introduction; 8.2 Dendrimer Synthesis; 8.2.1 Divergent Synthesis; 8.2.2 Convergent Synthesis; 8.3 Dendrimer Functionalization; 8.4 Conclusions and Future Directions; References 327 $a9 Reversible Diels-Alder Cycloaddition for the Design of Multifunctional Network Polymers 330 $aMimicking natural biochemical processes, click chemistry is a modular approach to organic synthesis, joining together small chemical units quickly, efficiently and predictably. In contrast to complex traditional synthesis, click reactions offer high selectivity and yields, near-perfect reliability and exceptional tolerance towards a wide range of functional groups and reaction conditions. These 'spring loaded' reactions are achieved by using a high thermodynamic driving force, and are attracting tremendous attention throughout the chemical community. Originally introduced with the focus on dru 606 $aBiotechnology 606 $aMaterials science 606 $aCombinatorial chemistry 606 $aMacromolecules$xSynthesis 615 0$aBiotechnology. 615 0$aMaterials science. 615 0$aCombinatorial chemistry. 615 0$aMacromolecules$xSynthesis. 676 $a620.11 676 $a660.6 701 $aLahann$b Joerg$01638647 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830267903321 996 $aClick chemistry for biotechnology and materials science$93981202 997 $aUNINA