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Bioconjugate chemistry
Bioconjugate chemistry
Pubbl/distr/stampa Washington, D.C., : American Chemical Society, ©1990-
Disciplina 574
Soggetto topico Bioconjugates
Bioconjugués
Soggetto genere / forma Periodicals.
Soggetto non controllato Microbiology & Immunology
ISSN 1520-4812
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti BC bioconjugate chemistry
Bioconjugate chem
Record Nr. UNISA-996439749403316
Washington, D.C., : American Chemical Society, ©1990-
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Bioconjugate chemistry
Bioconjugate chemistry
Pubbl/distr/stampa Washington, D.C., : American Chemical Society, ©1990-
Disciplina 574
Soggetto topico Bioconjugates
Bioconjugués
Soggetto genere / forma Periodicals.
Soggetto non controllato Microbiology & Immunology
ISSN 1520-4812
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Altri titoli varianti BC bioconjugate chemistry
Bioconjugate chem
Record Nr. UNINA-9910143393603321
Washington, D.C., : American Chemical Society, ©1990-
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chemistry of bioconjugates : synthesis, characterization, and biomedical applications / / edited by Ravin Narain
Chemistry of bioconjugates : synthesis, characterization, and biomedical applications / / edited by Ravin Narain
Pubbl/distr/stampa Hoboken, New Jersey : , : Wiley, , 2014
Descrizione fisica 1 online resource (495 p.)
Disciplina 612.1/111
Altri autori (Persone) NarainRavin
Soggetto topico Bioconjugates
ISBN 1-118-77637-2
1-118-77588-0
1-118-77640-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CHEMISTRY OF BIOCONJUGATES; CONTENTS; PREFACE; CONTRIBUTORS; SECTION I GENERAL METHODS OF BIOCONJUGATION; 1 COVALENT AND NONCOVALENT BIOCONJUGATION STRATEGIES; 1.1 INTRODUCTION; 1.2 COVALENT BIOCONJUGATION STRATEGIES; 1.2.1 Carboxyl Modifications; 1.2.2 Carbonyl Functional Groups; 1.2.3 Amine Modifications; 1.2.4 Thiol Modifications; 1.2.5 Hydroxyl Modifications; 1.2.6 Native Chemical Ligation and Expressed Protein Ligation; 1.2.7 Cross-linking Reagents for Bioconjugation; 1.2.8 Bioorthogonal Reactions; 1.2.9 Bioconjugation Via Transition Metal-catalyzed/Mediated Reactions
1.2.10 Other Covalent Bioconjugation Methods1.3 NONCOVALENT BIOCONJUGATION STRATEGIES; 1.3.1 Biotin-(Strept)Avidin System; 1.3.2 Electrostatic Interactions; 1.3.3 Metal-mediated Non-covalent Conjugation; 1.3.4 Hybridization Method; 1.4 CONCLUSIONS AND OUTLOOK; REFERENCES; SECTION II POLYMER BIOCONJUGATES; 2 BIOCONJUGATES BASED ON POLY(ETHYLENE GLYCOL)S AND POLYGLYCEROLS; 2.1 INTRODUCTION; 2.2 POLYETHYLENE GLYCOL-BASED BIOCONJUGATES; 2.2.1 PEG-protein Conjugates; 2.2.2 PEG-peptide Conjugates; 2.2.3 PEG-antibody Conjugates; 2.2.4 PEGylation of Cells and Tissues
2.2.5 PEG Conjugates of Oligonucleotides, Aptamers, and siRNAs2.2.6 PEG-drug Conjugates (PEG prodrugs); 2.2.7 PEGylation of Viruses; 2.3 LIMITATIONS OF PEG CONJUGATES; 2.4 POLYGLYCEROL-BASED CONJUGATES; 2.4.1 HPG-drug Conjugates; 2.4.2 HPG-peptide and Protein Conjugates; 2.4.3 HPG Glycoconjugates; 2.4.4 HPG-Red Blood Cell Conjugates for Antigen Protection; 2.5 CONCLUSIONS; ACKNOWLEDGMENTS; REFERENCES; 3 SYNTHETIC POLYMER BIOCONJUGATE SYSTEMS; 3.1 INTRODUCTION; 3.2 PEPTIDE OR PROTEIN BIOCONJUGATION TECHNIQUES; 3.2.1 Conjugation with Amino Acid; 3.2.2 Conjugation with Peptide Chain
3.2.3 Conjugation with Proteins3.3 CARBOHYDRATE BIOCONJUGATION TECHNIQUES; 3.4 CONJUGATION WITH NUCLEIC ACID; 3.5 CONJUGATION WITH DRUGS; 3.6 CONJUGATION WITH CONTRAST AGENTS; 3.6.1 Polymers for Magnetic Resonance Imaging; 3.6.2 Polymers for Optical Imaging; 3.6.3 Polymers for Nuclear imaging; 3.7 CONCLUSION AND PERSPECTIVE; REFERENCES; 4 NATURAL POLYMER BIOCONJUGATE SYSTEMS; 4.1 INTRODUCTION; 4.2 NATURAL POLYMER SYSTEMS; 4.2.1 Protein-origin Polymer Bioconjugates; 4.2.2 Polysaccharidic Polymer Bioconjugates; 4.3 CONCLUSION AND FUTURE DIRECTIONS; ACKNOWLEDGMENT; REFERENCES
5 DENDRIMER BIOCONJUGATES: SYNTHESIS AND APPLICATIONS5.1 INTRODUCTION-DENDRIMERS FOR BIOCONJUGATE CHEMISTRY; 5.2 DENDRIMER-DRUG CONJUGATES; 5.2.1 Motivation for the Development of Dendrimer-Drug Conjugates; 5.2.2 Dendrimer-DOX Conjugates; 5.2.3 Dendrimer-MTX Conjugates; 5.2.4 Dendrimer-TAX Conjugates; 5.2.5 Dendrimer-NAC Conjugates; 5.2.6 Dendrimer-Sulfonic Acids; 5.3 DENDRIMER-CARBOHYDRATE CONJUGATES; 5.3.1 Motivation for the Development of Dendrimer-Carbohydrate Conjugates; 5.3.2 Dendrimer-Mannose Conjugates; 5.3.3 Dendrimer-Galactose Conjugates; 5.3.4 Dendrimer-AcNA Conjugates
5.4 DENDRIMER CONJUGATES WITH IMAGING AGENTS
Record Nr. UNINA-9910140188603321
Hoboken, New Jersey : , : Wiley, , 2014
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chemistry of bioconjugates : synthesis, characterization, and biomedical applications / / edited by Ravin Narain
Chemistry of bioconjugates : synthesis, characterization, and biomedical applications / / edited by Ravin Narain
Pubbl/distr/stampa Hoboken, New Jersey : , : Wiley, , 2014
Descrizione fisica 1 online resource (495 p.)
Disciplina 612.1/111
Altri autori (Persone) NarainRavin
Soggetto topico Bioconjugates
ISBN 1-118-77637-2
1-118-77588-0
1-118-77640-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CHEMISTRY OF BIOCONJUGATES; CONTENTS; PREFACE; CONTRIBUTORS; SECTION I GENERAL METHODS OF BIOCONJUGATION; 1 COVALENT AND NONCOVALENT BIOCONJUGATION STRATEGIES; 1.1 INTRODUCTION; 1.2 COVALENT BIOCONJUGATION STRATEGIES; 1.2.1 Carboxyl Modifications; 1.2.2 Carbonyl Functional Groups; 1.2.3 Amine Modifications; 1.2.4 Thiol Modifications; 1.2.5 Hydroxyl Modifications; 1.2.6 Native Chemical Ligation and Expressed Protein Ligation; 1.2.7 Cross-linking Reagents for Bioconjugation; 1.2.8 Bioorthogonal Reactions; 1.2.9 Bioconjugation Via Transition Metal-catalyzed/Mediated Reactions
1.2.10 Other Covalent Bioconjugation Methods1.3 NONCOVALENT BIOCONJUGATION STRATEGIES; 1.3.1 Biotin-(Strept)Avidin System; 1.3.2 Electrostatic Interactions; 1.3.3 Metal-mediated Non-covalent Conjugation; 1.3.4 Hybridization Method; 1.4 CONCLUSIONS AND OUTLOOK; REFERENCES; SECTION II POLYMER BIOCONJUGATES; 2 BIOCONJUGATES BASED ON POLY(ETHYLENE GLYCOL)S AND POLYGLYCEROLS; 2.1 INTRODUCTION; 2.2 POLYETHYLENE GLYCOL-BASED BIOCONJUGATES; 2.2.1 PEG-protein Conjugates; 2.2.2 PEG-peptide Conjugates; 2.2.3 PEG-antibody Conjugates; 2.2.4 PEGylation of Cells and Tissues
2.2.5 PEG Conjugates of Oligonucleotides, Aptamers, and siRNAs2.2.6 PEG-drug Conjugates (PEG prodrugs); 2.2.7 PEGylation of Viruses; 2.3 LIMITATIONS OF PEG CONJUGATES; 2.4 POLYGLYCEROL-BASED CONJUGATES; 2.4.1 HPG-drug Conjugates; 2.4.2 HPG-peptide and Protein Conjugates; 2.4.3 HPG Glycoconjugates; 2.4.4 HPG-Red Blood Cell Conjugates for Antigen Protection; 2.5 CONCLUSIONS; ACKNOWLEDGMENTS; REFERENCES; 3 SYNTHETIC POLYMER BIOCONJUGATE SYSTEMS; 3.1 INTRODUCTION; 3.2 PEPTIDE OR PROTEIN BIOCONJUGATION TECHNIQUES; 3.2.1 Conjugation with Amino Acid; 3.2.2 Conjugation with Peptide Chain
3.2.3 Conjugation with Proteins3.3 CARBOHYDRATE BIOCONJUGATION TECHNIQUES; 3.4 CONJUGATION WITH NUCLEIC ACID; 3.5 CONJUGATION WITH DRUGS; 3.6 CONJUGATION WITH CONTRAST AGENTS; 3.6.1 Polymers for Magnetic Resonance Imaging; 3.6.2 Polymers for Optical Imaging; 3.6.3 Polymers for Nuclear imaging; 3.7 CONCLUSION AND PERSPECTIVE; REFERENCES; 4 NATURAL POLYMER BIOCONJUGATE SYSTEMS; 4.1 INTRODUCTION; 4.2 NATURAL POLYMER SYSTEMS; 4.2.1 Protein-origin Polymer Bioconjugates; 4.2.2 Polysaccharidic Polymer Bioconjugates; 4.3 CONCLUSION AND FUTURE DIRECTIONS; ACKNOWLEDGMENT; REFERENCES
5 DENDRIMER BIOCONJUGATES: SYNTHESIS AND APPLICATIONS5.1 INTRODUCTION-DENDRIMERS FOR BIOCONJUGATE CHEMISTRY; 5.2 DENDRIMER-DRUG CONJUGATES; 5.2.1 Motivation for the Development of Dendrimer-Drug Conjugates; 5.2.2 Dendrimer-DOX Conjugates; 5.2.3 Dendrimer-MTX Conjugates; 5.2.4 Dendrimer-TAX Conjugates; 5.2.5 Dendrimer-NAC Conjugates; 5.2.6 Dendrimer-Sulfonic Acids; 5.3 DENDRIMER-CARBOHYDRATE CONJUGATES; 5.3.1 Motivation for the Development of Dendrimer-Carbohydrate Conjugates; 5.3.2 Dendrimer-Mannose Conjugates; 5.3.3 Dendrimer-Galactose Conjugates; 5.3.4 Dendrimer-AcNA Conjugates
5.4 DENDRIMER CONJUGATES WITH IMAGING AGENTS
Record Nr. UNINA-9910820293303321
Hoboken, New Jersey : , : Wiley, , 2014
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chemoselective and bioorthogonal ligation reactions : concepts and applications / / edited by W. Russ Algar, Philip E. Dawson and Igor L. Medintz
Chemoselective and bioorthogonal ligation reactions : concepts and applications / / edited by W. Russ Algar, Philip E. Dawson and Igor L. Medintz
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , 2017
Descrizione fisica 1 electronic resource (756 p.)
Disciplina 612.11
Soggetto topico Bioconjugación
Bioconjugates
Soggetto genere / forma Electronic books.
ISBN 3-527-68347-X
3-527-68345-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910270893603321
Weinheim, Germany : , : Wiley-VCH, , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chemoselective and bioorthogonal ligation reactions : concepts and applications / / edited by W. Russ Algar, Philip E. Dawson and Igor L. Medintz
Chemoselective and bioorthogonal ligation reactions : concepts and applications / / edited by W. Russ Algar, Philip E. Dawson and Igor L. Medintz
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , 2017
Descrizione fisica 1 electronic resource (756 p.)
Disciplina 612.11
Soggetto topico Bioconjugación
Bioconjugates
ISBN 3-527-68347-X
3-527-68345-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chemistries. A Brief Introduction to Traditional Bioconjugate Chemistry / W Russ Algar -- [3+2]-Dipolar Cycloadditions in Bioconjugation / Jason E Hein -- Diels-Alder and Inverse Diels-Alder Reactions / Roberto J Brea, Neal K Devaraj -- The Staudinger Ligation / Olaia Nieto-García, Marcie B Jaffee, Michaela Mühlberg, Christian P R Hackenberger -- Thiol-Ene Chemistry / Neil B Cramer, Christopher N Bowman -- Ligand-Directed Tosyl and Acyl Imidazole Chemistry / Kazuya Matsuo, Itaru Hamachi -- Bioorthogonal Labeling of Cellular Proteins by Enzymatic and Related Mechanisms / Scott A Walper, Kendrick B Turner, Igor L Medintz -- Metal-Mediated Bioconjugation / Justin M Chalker -- Front Matter -- Applications. Protein and Antibody Labeling / Angela M Mariani, Kim E Sapsford -- Activity-Based Protein Profiling / Eliane V Wolf, Steven H L Verhelst -- Nucleic Acid Labeling, Ligation, and Modification / Afaf H El-Sagheer, Tom Brown -- Chemoselective Reactions for Glycan Labeling / Janet E McCombs, Jennifer J Kohler -- Chemoselective Attachment of Lipids to Proteins / Christian F W Becker -- In Vivo Applications of Bioorthogonal Chemistries / Chelsea G Gordon, Carolyn R Bertozzi -- Immobilization of Biomolecular Probes for Arrays and Assay: Critical Aspects of Biointerfaces / Stella H North, Chris Rowe Taitt -- Chemical Ligations in the Design of Hydrogel Materials / Scott H Medina, Joel P Schneider -- Nanoparticle Bioconjugates: Materials that Benefit from Chemoselective and Bioorthogonal Ligation Chemistries / Melissa Massey, W Russ Algar -- Application of Engineered Viral Nanoparticles in Materials and Medicine / Michael D Glidden, John F Edelbrock, Amy M Wen, Sourabh Shukla, Yingfang Ma, Roger H French, Jonathan K Pokorski, Nicole F Steinmetz.
Record Nr. UNINA-9910830978403321
Weinheim, Germany : , : Wiley-VCH, , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Cross conjugation : modern dendralene, radialene and fulvene chemistry / / edited by Henning Hopf and Michael S. Sherburn
Cross conjugation : modern dendralene, radialene and fulvene chemistry / / edited by Henning Hopf and Michael S. Sherburn
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , 2016
Descrizione fisica 1 online resource (601 p.)
Disciplina 612.1111
Soggetto topico Bioconjugates
Soggetto genere / forma Electronic books.
ISBN 3-527-67118-8
3-527-67121-8
3-527-67120-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Title Page; Copyright; Table of Contents; List of Contributors; Preface; Chapter 1: Synthesis of Dendralenes; 1.1 Introduction; 1.2 Multibond Forming Processes; 1.3 Solo-Bond-Forming Reactions; 1.4 Dendralenes from Dendralenes; 1.5 Functional Group Interconversion Reactions; 1.6 Concluding Remarks; References; Chapter 2: The Diene-Transmissive Hetero-Diels-Alder Reaction; 2.1 Introduction; 2.2 DTHDA Reaction of Heterotrienes; 2.3 DTHDA Reaction with Heterodienophiles; References; Chapter 3: The Nazarov Cyclization of Cross-Conjugated Ketones; 3.1 Introduction; 3.2 Mechanism
3.3 Substituent Effects3.4 Interrupted Nazarov Reactions; References; Chapter 4: [n]Radialenes; 4.1 Introduction; 4.2 Syntheses and Reactivity; 4.3 Structural and Bonding Properties; References; Chapter 5: Oxocarbons, Pseudo-oxocarbons, and Squaraines; 5.1 Introduction; 5.2 Oxocarbons and Coordination Chemistry; 5.3 Pseudo-oxocarbons; 5.4 Conclusion and Outlook; References; Chapter 6: Recent Developments in Fulvene and Heterofulvene Chemistry; 6.1 Introduction; 6.2 Triafulvenes; 6.3 Pentafulvenes and Related Compounds; 6.4 Heptafulvenes; 6.5 Other Fulvenes; References
Chapter 7: Constructing Molecular Complexity and Diversity by Cycloaddition Reactions of Fulvenes7.1 Introduction; 7.2 Reactions of Pentafulvenes; 7.3 Reactions of Heptafulvenes; 7.4 Reactions of Triafulvenes; 7.5 Conclusions; Acknowledgments; References; Chapter 8: Cross-Conjugation and Electronic Structure in TTF Analogs; 8.1 Introduction; 8.2 Dendralene-Type TTF Analogs and Related Compounds; 8.3 Radialene-Type TTF Analogs (DT-Substituted Radialenes); 8.4 Cross-Conjugated TTFs and Related Compounds Linked by π-Systems; References; Chapter 9: Cross-Conjugation in Expanded Systems
9.1 Introduction9.2 Tetrathiafulvalene and Dithiafulvene; 9.3 Communication between Two Identical Redox Centers; 9.4 Cross-Conjugation and Optical Properties; 9.5 Conjugation and Molecular Electronics; 9.6 Conclusions; References; Chapter 10: Transition Metal Complexes of Cross-Conjugated π Systems; 10.1 Introduction; 10.2 Trimethylenemethane Complexes; 10.3 Fulvene Complexes; 10.4 Fulvalene Complexes; 10.5 Azulene Complexes; 10.6 Pentalene and Acepentalene Complexes; 10.7 Various Complexes; References; Chapter 11: Cross-Conjugation and Quantum Interference; 11.1 Introduction
11.2 Molecular Electron Transport11.3 The Transport Properties of Cross-Conjugated Molecules; 11.4 Understanding and Predicting Interference; 11.5 More than Topology; 11.6 Conclusions; References; Chapter 12: Cross-Conjugation in Synthesis; 12.1 The Rapid Generation of Structural Complexity; 12.2 Diene-Transmissive Diels-Alder Reactions; 12.3 [3]Dendralenes; 12.4 Higher Dendralenes; 12.5 Applications; 12.6 The Radialenes; 12.7 Concluding Remarks; References; Author Index; Subject Index; End User License Agreement
Record Nr. UNINA-9910136778503321
Weinheim, Germany : , : Wiley-VCH, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Cross conjugation : modern dendralene, radialene and fulvene chemistry / / edited by Henning Hopf and Michael S. Sherburn
Cross conjugation : modern dendralene, radialene and fulvene chemistry / / edited by Henning Hopf and Michael S. Sherburn
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , 2016
Descrizione fisica 1 online resource (601 p.)
Disciplina 612.1111
Soggetto topico Bioconjugates
ISBN 3-527-67118-8
3-527-67121-8
3-527-67120-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Title Page; Copyright; Table of Contents; List of Contributors; Preface; Chapter 1: Synthesis of Dendralenes; 1.1 Introduction; 1.2 Multibond Forming Processes; 1.3 Solo-Bond-Forming Reactions; 1.4 Dendralenes from Dendralenes; 1.5 Functional Group Interconversion Reactions; 1.6 Concluding Remarks; References; Chapter 2: The Diene-Transmissive Hetero-Diels-Alder Reaction; 2.1 Introduction; 2.2 DTHDA Reaction of Heterotrienes; 2.3 DTHDA Reaction with Heterodienophiles; References; Chapter 3: The Nazarov Cyclization of Cross-Conjugated Ketones; 3.1 Introduction; 3.2 Mechanism
3.3 Substituent Effects3.4 Interrupted Nazarov Reactions; References; Chapter 4: [n]Radialenes; 4.1 Introduction; 4.2 Syntheses and Reactivity; 4.3 Structural and Bonding Properties; References; Chapter 5: Oxocarbons, Pseudo-oxocarbons, and Squaraines; 5.1 Introduction; 5.2 Oxocarbons and Coordination Chemistry; 5.3 Pseudo-oxocarbons; 5.4 Conclusion and Outlook; References; Chapter 6: Recent Developments in Fulvene and Heterofulvene Chemistry; 6.1 Introduction; 6.2 Triafulvenes; 6.3 Pentafulvenes and Related Compounds; 6.4 Heptafulvenes; 6.5 Other Fulvenes; References
Chapter 7: Constructing Molecular Complexity and Diversity by Cycloaddition Reactions of Fulvenes7.1 Introduction; 7.2 Reactions of Pentafulvenes; 7.3 Reactions of Heptafulvenes; 7.4 Reactions of Triafulvenes; 7.5 Conclusions; Acknowledgments; References; Chapter 8: Cross-Conjugation and Electronic Structure in TTF Analogs; 8.1 Introduction; 8.2 Dendralene-Type TTF Analogs and Related Compounds; 8.3 Radialene-Type TTF Analogs (DT-Substituted Radialenes); 8.4 Cross-Conjugated TTFs and Related Compounds Linked by π-Systems; References; Chapter 9: Cross-Conjugation in Expanded Systems
9.1 Introduction9.2 Tetrathiafulvalene and Dithiafulvene; 9.3 Communication between Two Identical Redox Centers; 9.4 Cross-Conjugation and Optical Properties; 9.5 Conjugation and Molecular Electronics; 9.6 Conclusions; References; Chapter 10: Transition Metal Complexes of Cross-Conjugated π Systems; 10.1 Introduction; 10.2 Trimethylenemethane Complexes; 10.3 Fulvene Complexes; 10.4 Fulvalene Complexes; 10.5 Azulene Complexes; 10.6 Pentalene and Acepentalene Complexes; 10.7 Various Complexes; References; Chapter 11: Cross-Conjugation and Quantum Interference; 11.1 Introduction
11.2 Molecular Electron Transport11.3 The Transport Properties of Cross-Conjugated Molecules; 11.4 Understanding and Predicting Interference; 11.5 More than Topology; 11.6 Conclusions; References; Chapter 12: Cross-Conjugation in Synthesis; 12.1 The Rapid Generation of Structural Complexity; 12.2 Diene-Transmissive Diels-Alder Reactions; 12.3 [3]Dendralenes; 12.4 Higher Dendralenes; 12.5 Applications; 12.6 The Radialenes; 12.7 Concluding Remarks; References; Author Index; Subject Index; End User License Agreement
Record Nr. UNINA-9910830976503321
Weinheim, Germany : , : Wiley-VCH, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui