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Domino Reactions : Concepts for Efficient Organic Synthesis.

The follow-up to the successful ""Domino Reaction in Organic Synthesis"", this ready reference brings up to date on the original concept. The chapters have been arranged according to the name of well-known transformations of the first step and in combination with the formed produ...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Tietze, Lutz F.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Hoboken : Wiley, 2013.
Temas:
Acceso en línea:Texto completo
Tabla de Contenidos:
  • Domino Reactions; Contents; Preface; List of Contributors; List of Abbreviations; Chapter Introduction; References; Chapter 1 Transition-Metal-Catalyzed Carbonylative Domino Reactions; 1.1 Introduction; 1.2 Transition-Metal-Catalyzed Carbonylative Domino Reactions; 1.2.1 Ruthenium-Catalyzed Carbonylative Domino Reactions; 1.2.2 Rhodium-Catalyzed Carbonylative Domino Reactions; 1.2.3 Palladium-Catalyzed Carbonylative Domino Reactions; 1.2.4 Iron-, Copper-, Nickel-, and Cobalt-Catalyzed Carbonylative Domino Reactions; 1.3 Outlook; References; Chapter 2 Metathesis Reactions in Domino Processes.
  • 2.1 Domino Processes Featuring Solely Metathesis Events2.1.1 Reactions Involving Only Alkenes; 2.1.2 Reactions Involving Alkenes and Alkynes; 2.2 Domino Processes Featuring Metathesis and Non-metathesis Events; 2.2.1 Metathesis/Redox Transformation; 2.2.2 Metathesis/Isomerization; 2.2.3 Metathesis/Cycloaddition; 2.2.4 Metathesis/Substitution; 2.2.5 Metathesis/Conjugate Addition; 2.2.6 Metathesis/Carbonyl Olefination; 2.3 Conclusion and Outlook; Acknowledgments; References; Chapter 3 C-H Activation Reactions in Domino Processes; 3.1 Heck Reactions/C-H Activations.
  • 3.2 Carbopalladations and Aminopalladations of Alkynes/C-H Activations3.3 Palladium-Catalyzed/Norbornene-Mediated ortho C-H Activations; 3.4 Domino Reactions Involving Heteroatom-Directed C-H Activations; 3.5 Conclusions; References; Chapter 4 Domino Reactions Initiated by Nucleophilic Substitution; 4.1 Domino SN/Michael Addition and Related Reactions; 4.2 Domino Reactions Initiated by Nucleophilic Ring Opening of Aziridines, Epoxides, and Activated Cyclopropanes; 4.3 Domino SN/Brook Rearrangements; References; Chapter 5 Radical Reactions in Domino Processes; 5.1 Introduction.
  • 5.2 Radical/Cation Domino Processes5.3 Radical/Anionic Domino Processes; 5.4 Domino Radical/Radical Process; 5.5 Radical/Pericyclic Domino Processes; 5.6 Asymmetric Radical Domino Processes; 5.6.1 Chiral Auxiliary-Directed Asymmetric Radical Domino Processes; 5.6.2 Chiral Catalyst-Driven Asymmetric Radical Domino Processes; 5.7 Conclusion and Outlook; Acknowledgments; References; Chapter 6 Pericyclic Reactions in Domino Processes; 6.1 Introduction; 6.2 Cycloadditions; 6.2.1 Cycloaddition/Cycloaddition; 6.2.2 Cycloaddition/Cycloreversion; 6.2.3 Cycloaddition/Sigmatropic Rearrangement.
  • 6.2.4 Cycloaddition/Electrocyclization6.2.5 Cycloaddition/Mixed Transformations; 6.3 Sigmatropic Rearrangements; 6.3.1 Sigmatropic Rearrangement/Sigmatropic Rearrangement; 6.3.2 Sigmatropic Rearrangement/Cycloaddition; 6.3.3 Sigmatropic Rearrangement/Electrocyclization; 6.3.4 Sigmatropic Rearrangement/Mixed Transformations; 6.4 Electrocyclizations; 6.4.1 Electrocyclization/Electrocyclization; 6.4.2 Electrocyclization/Cycloaddition; 6.4.3 Electrocyclization/Sigmatropic Rearrangement; 6.4.4 Electrocyclization/Mixed Transformations; 6.5 Mixed Transformations.