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Catalytic arylation methods : from the academic lab to industrial processes / / Anthony J. Burke and Carolina Silva Marques
| Catalytic arylation methods : from the academic lab to industrial processes / / Anthony J. Burke and Carolina Silva Marques |
| Autore | Burke Anthony J. |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmbH & KGaA, , [2015] |
| Descrizione fisica | 1 online resource (1058 p.) |
| Disciplina | 541.395 |
| Soggetto topico | Arylation |
| ISBN |
3-527-67274-5
3-527-67270-2 3-527-67285-0 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Related Titles; Title Page; Copyright; Dedication; Preface; List of Abbreviations; Chapter 1: Cross-Coupling Arylations: Precedents and Rapid HistoricalReview of the Field; 1.1 Metal-Catalyzed Cross-Couplings: From Its Origins to the Nobel Prize and Beyond; 1.2 Arylation: What Is So Special?; 1.3 Recent New Developments; 1.4 Selected Experiments from the Literature; References; Chapter 2: Amine, Phenol, Alcohol, and Thiol Arylation; 2.1 Introduction; 2.2 Pd-Catalyzed Processes; 2.3 Cu-Catalyzed and Promoted Arylations: (CAr-N Bond Formation); 2.4 Fe-Catalyzed Arylations
2.5 Ni-Catalyzed Reactions2.6 Co-Catalyzed Arylations; 2.7 Mn-Catalyzed Arylations; 2.8 Cd-Catalyzed Arylations; 2.9 Bi(III) and Indium Oxide-Catalyzed Thiol Arylations; 2.10 Conclusions and Final Comment; 2.11 Selected Experiments from the Literature; References; Chapter 3: Decarboxylative Coupling Techniques; 3.1 Introduction; 3.2 Pd-Catalyzed Versions; 3.3 Other Metal-Catalyzed Versions; 3.4 Conclusions; 3.5 Selected Experiments; References; Chapter 4: C-H Bond Activation for Arylations; 4.1 Introduction; 4.2 C(sp2)-H Activations; 4.3 Conclusions 4.4 Selected Experiments from the LiteratureReferences; Chapter 5: Conjugate Additions; 5.1 Conjugate Additions: A Powerful Tool for Appending Organic Residues to Cyclic and Acyclic Substrates; 5.2 Applications of Rh Catalysts; 5.3 Applications of Pd Catalysts; 5.4 Applications of Ru and Other Catalysts; 5.5 Conclusions; 5.6 Selected Experiments; References; Chapter 6: Imine Arylations - Synthesis of Arylamines; 6.1 Arylation of C=N Bonds: Simple Access to Chiral Amine Units; 6.2 Application of Rh Catalysts; 6.3 Application of Pd Catalysts; 6.4 Application of Ru and Other Catalysts 6.5 The Petasis-Akritopoulou Reaction6.6 Conclusions; 6.7 Selected Experiments; References; Chapter 7: Carbonyl Group Arylation; 7.1 Introduction; 7.2 Application of Rh Catalysts; 7.3 Application of Pd Catalysts; 7.4 Application of Ru and Other Catalysts; 7.5 Conclusions; 7.6 Selected Experiments; References; Chapter 8: α-Arylation Processes; 8.1 Introduction; 8.2 Arylation of Enolates and Equivalents; 8.3 Other Metal-Catalyzed α-Arylations; 8.4 Conclusions; 8.5 Selected Experiments; References; Chapter 9: Catalytic Cycloaddition Aromatization Processes; 9.1 Introduction 9.2 Cycloaddition Events9.3 Radical-Based Cycloaromatization Processes; 9.4 Conclusions; 9.5 Selected Experiments from the Literature; References; Index; End User License Agreement |
| Record Nr. | UNINA-9910132344403321 |
Burke Anthony J.
|
||
| Weinheim, Germany : , : Wiley-VCH Verlag GmbH & KGaA, , [2015] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Catalytic arylation methods : from the academic lab to industrial processes / / Anthony J. Burke and Carolina Silva Marques
| Catalytic arylation methods : from the academic lab to industrial processes / / Anthony J. Burke and Carolina Silva Marques |
| Autore | Burke Anthony J. |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmbH & KGaA, , [2015] |
| Descrizione fisica | 1 online resource (1058 p.) |
| Disciplina | 541.395 |
| Soggetto topico | Arylation |
| ISBN |
3-527-67274-5
3-527-67270-2 3-527-67285-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Related Titles; Title Page; Copyright; Dedication; Preface; List of Abbreviations; Chapter 1: Cross-Coupling Arylations: Precedents and Rapid HistoricalReview of the Field; 1.1 Metal-Catalyzed Cross-Couplings: From Its Origins to the Nobel Prize and Beyond; 1.2 Arylation: What Is So Special?; 1.3 Recent New Developments; 1.4 Selected Experiments from the Literature; References; Chapter 2: Amine, Phenol, Alcohol, and Thiol Arylation; 2.1 Introduction; 2.2 Pd-Catalyzed Processes; 2.3 Cu-Catalyzed and Promoted Arylations: (CAr-N Bond Formation); 2.4 Fe-Catalyzed Arylations
2.5 Ni-Catalyzed Reactions2.6 Co-Catalyzed Arylations; 2.7 Mn-Catalyzed Arylations; 2.8 Cd-Catalyzed Arylations; 2.9 Bi(III) and Indium Oxide-Catalyzed Thiol Arylations; 2.10 Conclusions and Final Comment; 2.11 Selected Experiments from the Literature; References; Chapter 3: Decarboxylative Coupling Techniques; 3.1 Introduction; 3.2 Pd-Catalyzed Versions; 3.3 Other Metal-Catalyzed Versions; 3.4 Conclusions; 3.5 Selected Experiments; References; Chapter 4: C-H Bond Activation for Arylations; 4.1 Introduction; 4.2 C(sp2)-H Activations; 4.3 Conclusions 4.4 Selected Experiments from the LiteratureReferences; Chapter 5: Conjugate Additions; 5.1 Conjugate Additions: A Powerful Tool for Appending Organic Residues to Cyclic and Acyclic Substrates; 5.2 Applications of Rh Catalysts; 5.3 Applications of Pd Catalysts; 5.4 Applications of Ru and Other Catalysts; 5.5 Conclusions; 5.6 Selected Experiments; References; Chapter 6: Imine Arylations - Synthesis of Arylamines; 6.1 Arylation of C=N Bonds: Simple Access to Chiral Amine Units; 6.2 Application of Rh Catalysts; 6.3 Application of Pd Catalysts; 6.4 Application of Ru and Other Catalysts 6.5 The Petasis-Akritopoulou Reaction6.6 Conclusions; 6.7 Selected Experiments; References; Chapter 7: Carbonyl Group Arylation; 7.1 Introduction; 7.2 Application of Rh Catalysts; 7.3 Application of Pd Catalysts; 7.4 Application of Ru and Other Catalysts; 7.5 Conclusions; 7.6 Selected Experiments; References; Chapter 8: α-Arylation Processes; 8.1 Introduction; 8.2 Arylation of Enolates and Equivalents; 8.3 Other Metal-Catalyzed α-Arylations; 8.4 Conclusions; 8.5 Selected Experiments; References; Chapter 9: Catalytic Cycloaddition Aromatization Processes; 9.1 Introduction 9.2 Cycloaddition Events9.3 Radical-Based Cycloaromatization Processes; 9.4 Conclusions; 9.5 Selected Experiments from the Literature; References; Index; End User License Agreement |
| Record Nr. | UNINA-9910824523003321 |
|
Burke Anthony J.
|
||
| Weinheim, Germany : , : Wiley-VCH Verlag GmbH & KGaA, , [2015] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
