Domino reactions in organic synthesis [[electronic resource] /] / Lutz F. Tietze, Gordon Brasche, and Kersten M. Gericke

• Record Nr.: UNINA9910144299003321
• Autore: Tietze Lutz-Friedjan
• Pubbl/distr/stampa: Weinheim, : Wiley-VCH, c2006
• ISBN: 1-280-72267-3; 9786610722679; 3-527-60992-X; 3-527-60868-0
• Descrizione fisica: 1 online resource (633 p.)
• Altri autori (Persone): BrascheGordon <1976->; GerickeKersten M. <1976->
• Disciplina: 547.1393
• Soggetti: Organic compounds - Synthesis; Chemical reactions; Electronic books.
• Lingua di pubblicazione: Inglese
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Note generali: Description based upon print version of record.
• Nota di bibliografia: Includes bibliographical references and index.
• Nota di contenuto: Domino Reactions in Organic Synthesis; Table of Contents; Preface; Abbreviations; Introduction; Classification; 1 Cationic Domino Reactions; 1.1 Cationic/Cationic Processes; 1.1.1 Cationic/Cationic/Cationic Processes; 1.2 Cationic/Pericyclic Processes; 1.3 Cationic/Reductive Processes; 2 Anionic Domino Reactions; 2.1 Anionic/Anionic Processes; 2.1.1 Anionic/Anionic/Anionic Processes; 2.1.2 Fourfold and Higher Anionic Processes; 2.1.3 Two- and Threefold Anionic Processes Followed by a Nonanionic Process; 2.2 Anionic/Radical Processes; 2.3 Anionic/Pericyclic Processes; 2.3.1 Anionic/Pericyclic Processes Followed by Further Transformations2.4 Anionic/Transition Metal-Catalyzed Processes; 2.5 Anionic/Oxidative or Reductive Processes; 3 Radical Domino Reactions; 3.1 Radical/Cationic Domino Processes; 3.2 Radical/Anionic Domino Processes; 3.3 Radical/Radical Domino Processes; 3.3.1 Radical/Radical/Anionic Domino Processes; 3.3.2 Radical/Radical/Radical Domino Processes; 3.3.3 Radical/Radical/Pericyclic Domino Processes; 3.3.4 ; Radical/Radical/Oxidation Domino Processes; 3.4 Radical/Pericyclic Domino Processes; 4 Pericyclic Domino Reactions; 4.1 Diels-Alder Reactions4.1.1 Diels-Alder/Diels-Alder Reactions; 4.1.2 Diels-Alder Reactions/Sigmatropic Rearrangements; 4.1.3 Diels-Alder/Retro-Diels-Alder Reactions; 4.1.4 Diels-Alder Reactions/Mixed Transformations; 4.1.5 Hetero-Diels-Alder Reactions; 4.2 1,3-Dipolar Cycloadditions; 4.3 [2+2] and Higher Cycloadditions; 4.4 Sigmatropic Rearrangements; 4.5 Electrocyclic Reactions; 4.6 Ene Reactions; 4.7 Retro-Pericyclic Reactions; 5 Photochemically Induced Domino Processes; 5.1 Photochemical/Cationic Domino Processes; 5.2 Photochemical/Anionic Domino Processes; 5.3 Photochemical/Radical Domino Processes5.4 Photochemical/Pericyclic Domino Processes; 5.5 Photochemical/Photochemical Domino Processes; 5.6 Photochemical/Transition Metal-Catalyzed Domino Processes; 6 Transition Metal-Catalyzed Domino Reactions; 6.1 Palladium-Catalyzed Transformations; 6.1.1 The Heck Reaction; 6.1.1.1 Domino Heck Reactions; 6.1.1.2 Heck/Cross-Coupling Reactions; 6.1.1.3 Heck/Tsuji-Trost Reactions; 6.1.1.4 Heck Reactions/CO-Insertions; 6.1.1.5 Heck Reactions/C-H-Activations; 6.1.1.6 Heck Reactions: Pericyclic Transformations; 6.1.1.7 Heck Reactions/Mixed Transformations; 6.1.2 Cross-Coupling Reactions6.1.2.1 Suzuki Reactions; 6.1.2.2 Stille Reactions; 6.1.2.3 Sonogashira Reactions; 6.1.2.4 Other Cross-Coupling Reactions; 6.1.3 Nucleophilic Substitution (Tsuji-Trost Reaction); 6.1.4 Reactions of Alkynes and Allenes; 6.1.5 Other Pd(0)-Catalyzed Transformations; 6.1.6 Pd(II)-Catalyzed Transformations; 6.2 Rhodium-Catalyzed Transformations; 6.2.1 Formation of Carbenes; 6.2.2 Hydroformylations; 6.2.3 Other Rhodium-Catalyzed Transformations; 6.3 Ruthenium-Catalyzed Transformations; 6.3.1 Metathesis Reactions; 6.3.1.1 Metathesis-Metathesis Processes; 6.3.1.2 Metathesis/Heck Reaction/Pericyclic Reaction/Hydrogenation
• Sommario/riassunto: Domino reactions enable you to build complex structures in one-pot reactions without the need to isolate intermediates- a dream comes true. In this book, the well-respected expert, Professor Lutz Tietze, summarizes the possibilities of this reaction type - an approach for an efficiant, economically benificial and ecologicalbenign synthesis.A definite must for every organic chemist.