Bioconjugate techniques / Greg T. Hermanson |
Autore | Hermanson, Greg T. |
Edizione | [3rd ed] |
Descrizione fisica | xvii, 1146 pages : illustrations ; 28 cm |
Disciplina | 612.1111 |
Soggetto topico |
Bioconjugates - Synthesis
Biomolecules - Researches - Diagnostics - Therapeutics |
ISBN | 9780123822390 (hbk) |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNISALENTO-991003689769707536 |
Hermanson, Greg T.
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Lo trovi qui: Univ. del Salento | ||
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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 | ||
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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 |
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 | ||
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Lo trovi qui: Univ. Federico II | ||
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A Novel Heme-Thiolate Peroxygenase AaeAPO and Its Implications for C-H Activation Chemistry / / by Xiaoshi Wang |
Autore | Wang Xiaoshi |
Edizione | [1st ed. 2016.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016 |
Descrizione fisica | 1 online resource (153 p.) |
Disciplina | 612.1111 |
Collana | Springer Theses, Recognizing Outstanding Ph.D. Research |
Soggetto topico |
Organic chemistry
Enzymology Catalysis Organic Chemistry |
ISBN | 3-319-03236-4 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | From the Contents: Hydrocarbon Oxygenation by Heme-Thiolate Enzymes -- Efficient and Selective Alkane Hydroxylation Reactions Catalyzed by the Fungal Peroxygenase AaeAPO -- Hydrocarbon Hydroxylations Catalyzed by AaeAPO: Evidence of Radical Intermediates and Kinetic Isotope Effects. |
Record Nr. | UNINA-9910254057303321 |
Wang Xiaoshi
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Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016 | ||
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Lo trovi qui: Univ. Federico II | ||
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