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Catalytic cascade reactions /
"The development of catalytic versions of cascade reactions has become one of the most active and burgeoning reaction areas in organic synthesis. Covering both organocatalysis and transition-metal catalysis for these reactions, Catalytic Cascade Reactions illustrates the versatility and applica...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Hoboken, New Jersey :
Wiley,
[2013]
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| Temas: | |
| Acceso en línea: | Texto completo |
MARC
| LEADER | 00000cam a2200000 i 4500 | ||
|---|---|---|---|
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| 245 | 0 | 0 | |a Catalytic cascade reactions / |c edited by Dr. Peng-Fei Xu and Dr. Wei Wang. |
| 264 | 1 | |a Hoboken, New Jersey : |b Wiley, |c [2013] | |
| 300 | |a 1 online resource | ||
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| 520 | |a "The development of catalytic versions of cascade reactions has become one of the most active and burgeoning reaction areas in organic synthesis. Covering both organocatalysis and transition-metal catalysis for these reactions, Catalytic Cascade Reactions illustrates the versatility and application of cascade reactions for synthesizing valuable compounds, such as drugs and natural products. Highlighting catalytic versus non-catalytic reactions, an important shift in academic and industry practice, the text brings chemists and the organic synthesis community up to speed on the many recent advances in the field"-- |c Provided by publisher. | ||
| 520 | |a "This book covers recent and important discoveries and activities in catalytic cascade reactions, an emerging and dynamic direction for organic synthesis"-- |c Provided by publisher. | ||
| 504 | |a Includes bibliographical references and index. | ||
| 588 | 0 | |a Print version record and CIP data provided by publisher. | |
| 505 | 0 | |a Catalytic Cascade Reactions -- Copyright -- Contents -- Contributors -- Preface -- 1 Amine-Catalyzed Cascade Reactions -- 1.1 Introduction -- 1.2 Enamine-Activated Cascade Reactions -- 1.2.1 Enamine-Enamine Cascades -- 1.2.1.1 Design of Enamine-Enamine Cascades -- 1.2.1.2 Examples of Enamine-Enamine and Enamine-Enamine Cyclization Cascades -- 1.2.1.3 Enamine-Enamine in Three-Component Cascades -- 1.2.1.4 Enamine-Activated Double a-Functionalization -- 1.2.1.5 Robinson Annulations -- 1.2.2 Enamine-Iminium Cascades -- 1.2.2.1 Design of Enamine-Iminium Cascades -- 1.2.2.2 Examples of [4 + 2] Reactions with Enamine-Activated Dienes -- 1.2.2.3 Inverse-Electron-Demand [4 + 2] Reactions with Enamine-Activated Dienophiles -- 1.2.2.4 Enamine-Iminium-Enamine Cascades -- 1.2.3 Enamine Catalysis Cyclization -- 1.2.3.1 Design of Enamine-Cyclization Cascade Reactions -- 1.2.3.2 Enamine-Intermolecular Addition Cascades -- 1.2.3.3 Enamine-Intramolecular Addition Cascades -- 1.2.3.4 Enamine-Intramolecular Aldol Cascades -- 1.3 Iminium-Initiated Cascade Reactions -- 1.3.1 Design of Iminium-Enamine Cascade Reactions -- 1.3.2 Iminium-Activated Diels-Alder Reactions -- 1.3.3 Iminium-Activated Sequential [4+2] Reactions -- 1.3.4 Iminium-Activated [3+2] Reactions -- 1.3.5 Iminium-Activated Sequential [3+2] Reactions -- 1.3.6 Iminium-Activated [2+1] Reactions -- 1.3.6.1 Iminium-Activated Cyclopropanations -- 1.3.6.2 Iminium-Activated Epoxidations -- 1.3.6.3 Iminium-Activated Aziridinations -- 1.3.7 Iminium-Activated Multicomponent Reactions -- 1.3.8 Iminium-Activated [3+3] Reactions -- 1.3.8.1 Iminium-Activated All-Carbon-Centered [3+3] Reactions -- 1.3.8.2 Imin ium-Activated Hetero-[3+3] Reactions -- 1.3.9 Other Iminium-Activated Cascade Reactions -- 1.4 Cycle-Specific Catalysis Cascades -- 1.5 Other Strategies -- 1.6 Summary and Outlook -- References. | |
| 505 | 8 | |a 2 Brønsted Acid-Catalyzed Cascade Reactions -- 2.1 Introduction -- 2.2 Protonic Acid-Catalyzed Cascade Reactions -- 2.2.1 Mannich Reaction -- 2.2.2 Pictect-Spengler Reaction -- 2.2.3 Biginelli Reaction -- 2.2.4 Povarov Reaction -- 2.2.5 Reduction Reaction -- 2.2.6 1,3-Dipolar Cycloaddition -- 2.2.7 Darzen Reaction -- 2.2.8 Acyclic Aminal and Hemiaminal Synthesis -- 2.2.9 Rearrangement Reaction -- 2.2.10 a, b -Unsaturated Imine-Involved Cyclization Reaction -- 2.2.11 Alkylation Reaction -- 2.2.12 Desymmetrization Reaction -- 2.2.13 Halocyclization -- 2.2.14 Redox Reaction -- 2.2.15 Isocyanide-Involved Multicomponent Reaction -- 2.2.16 Other Protonic Acid-Catalyzed Cascade Reactions -- 2.3 Chiral Thiourea (Urea)-Catalyzed Cascade Reactions -- 2.3.1 Neutral Activation -- 2.3.1.1 Halolactonization -- 2.3.1.2 Mannich Reaction -- 2.3.1.3 Michael-Aldol Reaction -- 2.3.1.4 Michael-Alkylation Reaction -- 2.3.1.5 Cyano-Involved Michael-Cyclization Reaction -- 2.3.1.6 Michael-Hemiketalization (Hemiacetalization) Reaction -- 2.3.1.7 Michael-Henry Reaction -- 2.3.1.8 Michael-Michael Reaction -- 2.3.1.9 Petasis Reaction -- 2.3.1.10 Sulfur Ylide-Involved Michael-Cyclization Reaction -- 2.3.1.11 a-Isothiocyanato Imide-Involved Cascade Reaction -- 2.3.1.12 a-Isocyanide-Involved Cascade Reaction -- 2.3.2 Anion-Binding Catalysis -- 2.3.2.1 Pictet-Spengler Reaction -- 2.3.2.2 Other Iminium Ion-Involved Cascade Reaction -- 2.3.2.3 Oxocarbenium Ion-Involved Cascade Reaction -- 2.4 Brønsted Acid and Transition Metal Cooperatively Catalyzed Cascade Reactions -- 2.4.1 Dual Catalysis -- 2.4.2 Cascade Catalysis -- 2.4.2.1 Pd(0)/Brønsted Acid System -- 2.4.2.2 Ruthenium/Brønsted Acid System -- 2.4.2.3 Au(I)/Brønsted Acid System -- 2.4.2.4 Other Binary Catalytic Systems -- 2.5 Conclusions -- References. | |
| 505 | 8 | |a 3 Application of Organocatalytic Cascade Reactions in Natural Product Synthesis and Drug Discovery -- 3.1 Introduction -- 3.2 Amine-Catalyzed Cascade Reactions in Natural Product Synthesis -- 3.2.1 Iminium-Ion-Catalyzed Cascade Reactions in Natural Product Synthesis -- 3.2.2 Cycle-Specific Cascade Catalysis in Natural Product Synthesis -- 3.2.2.1 Iminium-Enamine Cycle-Specific Cascade Catalysis -- 3.2.2.2 Enamine (/Dienamine)-Iminium Cycle-Specific Cascade Catalysis -- 3.2.2.3 More Complex Cycle-Specific Cascade Catalysis -- 3.3 Brønsted Acid-Catalyzed Cascade Reactions in Natural Product Synthesis -- 3.4 Bifunctional Base/Brønsted Acid-Catalyzed Cascade Reactions in Natural Product Synthesis -- 3.5 Summary and Outlook -- References -- 4 Gold-Catalyzed Cascade Reactions -- 4.1 Introduction -- 4.2 Cascade Reactions of Alkynes -- 4.2.1 Cascade Reactions of Enynes -- 4.2.1.1 Cascade Reactions of 1,6-Enynes -- 4.2.1.2 Cascade Reactions of 1,5-Enynes -- 4.2.1.3 Cascade Reactions of 1,4-Enynes -- 4.2.1.4 Cascade Reactions of 1,3-Enynes -- 4.2.1.5 Cascade Reactions of 1,n-Enynes (n> 6) -- 4.2.2 Cascade Reactions of Propargyl Carboxylates -- 4.2.3 Cascade Reactions of ortho-Substituted Arylalkynes -- 4.2.4 Cascade Reactions of Other Alkynes -- 4.3 Cascade Reactions of Allenes -- 4.4 Cascade Reactions of Alkenes and Cyclopropenes -- 4.5 Closing Remarks -- References -- 5 Cascade Reactions Catalyzed by Ruthenium, Iron, Iridium, Rhodium, and Copper -- 5.1 Introduction -- 5.2 Ruthenium-Catalyzed Transformations -- 5.3 Iron-Catalyzed Transformations -- 5.4 Iridium-Catalyzed Transformations -- 5.5 Rhodium-Catalyzed Transformations -- 5.6 Copper-Catalyzed Transformations -- 5.7 Miscellaneous Catalytic Reactions -- 5.8 Summary -- References -- 6 Palladium-Catalyzed Cascade Reactions of Alkenes, Alkynes, and Allenes -- 6.1 Introduction. | |
| 505 | 8 | |a 6.2 Cascade Reactions Involving Alkenes -- 6.2.1 Double Mizoroki-Heck Reaction Cascade -- 6.2.2 Cascade Heck Reaction/C-H Activation -- 6.2.3 Cascade Heck Reaction/Reduction/ Cyclization -- 6.2.4 Cascade Heck Reaction/Carbonylation -- 6.2.5 Cascade Heck Reaction/ Suzuki Coupling -- 6.2.6 Cascade Amino-/Oxopalladation/Carbopalladation Reaction -- 6.3 Cascade Reactions Involving Alkynes -- 6.3.1 Cascade Heck Reactions -- 6.3.2 Cascade Heck/Suzuki Coupling -- 6.3.3 Cationic Palladium(II)-Catalyzed Cascade Reactions -- 6.3.4 Cascade Heck Reaction/Stille Coupling -- 6.3.5 Cascade Heck/Sonogashira Coupling -- 6.3.6 Cascade Sonogashira Coupling-Cyclization -- 6.3.7 Cascade Heck and C-H Bond Functionalization -- 6.3.8 Cascade Reactions Initiated by Oxopalladation -- 6.3.9 Cascade Reactions Initiated by Aminopalladation -- 6.3.10 Cascade Reactions Initiated by Halopalladation or Acetoxypalladation -- 6.3.11 Cascade Reactions of 2-(1-Alkynyl)-alk-2-en-1-ones -- 6.3.12 Cascade Reactions of Propargylic Derivatives -- 6.4 Cascade Reactions Involving Allenes -- 6.4.1 Cascade Reactions of Monoallenes -- 6.4.2 Cross-Coupling Cyclization of Two Different Allenes -- 6.5 Summary and Outlook -- Acknowledgments -- References -- 7 Use of Transition Metal-Catalyzed Cascade Reactions in Natural Product Synthesis and Drug Discovery -- 7.1 Introduction -- 7.2 Palladium-Catalyzed Cascade Reactions in Total Synthesis -- 7.2.1 Cross-Coupling Reactions -- 7.2.1.1 Heck Reaction -- 7.2.1.2 Stille Reaction -- 7.2.1.3 Suzuki Coupling Reaction -- 7.2.2 Tsuji-Trost Reaction -- 7.2.3 Other Palladium-Catalyzed Cascade Reactions in Total Synthesis -- 7.3 Ruthenium-Catalyzed Cascade Reactions in Total Synthesis -- 7.4 Gold- and Platinum-Catalyzed Cascade Reactions in Organic Reactions -- 7.5 Copper- and Rhodium-Catalyzed Cascade Reactions in O rganic Synthesis -- 7.6 Summary -- References. | |
| 505 | 8 | |a 8 Engineering Mono- and Multifunctional Nanocatalysts for Cascade Reactions -- 8.1 Introduction -- 8.2 Heterogeneous Monofunctional Nanocatalysts -- 8.2.1 Metal-Based Monofunctional Nanocatalysts -- 8.2.2 Metal Oxide-Based Monofunctional Nanocatalysts -- 8.2.3 Orgamometallic-Based Monofunctional Nanocatalysts -- 8.2.4 Graphene Oxide-Based Monofunctional Nanocatalysts -- 8.3 Heterogeneous Multifunctional Nanocatalysts -- 8.3.1 Acid-Base Combined Multifunctional Nanocatalysts -- 8.3.2 Metal-Base Combined Multifunctional Nanocatalysts -- 8.3.3 Organometallic-Base Combined Multifunctional Nanocatalysts -- 8.3.4 Binary Organometallic-Based Multifunctional Nanocatalysts -- 8.3.5 Binary Metal-Based Multifunctional Nanocatalysts -- 8.3.6 Metal-Metal Oxide Combined Multifunctional Nanocatalysts -- 8.3.7 Organocatalyst-Acid Combined Multifunctional Nanocatalysts -- 8.3.8 Acid-Base-Metal Combined Multifunctional Nanocatalysts -- 8.3.9 Triple Enzyme-Based Multifunctional Nanocatalysts -- 8.4 Conclusions and Perspectives -- References -- 9 Multiple-Catalyst-Promoted Cascade Reactions -- 9.1 Introduction -- 9.2 Multiple Metal Catalyst-Promoted Cascade Reactions -- 9.2.1 Catalytic Systems Involving Palladium -- 9.2.2 Catalytic Systems Involving Other Metals -- 9.3 Multiple Organocatalyst-Promoted Cascade Reactions -- 9.3.1 Catalytic Systems Combining Multiple Amine Catalysts -- 9.3.2 Catalytic Systems Combining Amine Catalysts and Nucleophilic Carbenes -- 9.3.3 Catalytic Systems Combining Amine and Hydrogen-Bonding Donor Catalysts -- 9.3.4 Catalytic Systems Involving Other Organocatalysts -- 9.4 Metal/Organic Binary Catalytic System-Promoted Cascade Reactions -- 9.4.1 Catalytic Systems Combining Secondary Amine and Metal Catalysts -- 9.4.2 Catalytic Systems Combining Brønsted Acid and Metal Catalysts. | |
| 590 | |a ProQuest Ebook Central |b Ebook Central Academic Complete | ||
| 650 | 0 | |a Organic reaction mechanisms. | |
| 650 | 0 | |a Catalysis. | |
| 650 | 0 | |a Chemical reactions. | |
| 650 | 0 | |a Organic compounds |x Synthesis. | |
| 650 | 2 | |a Catalysis | |
| 650 | 6 | |a Réactions organiques (Chimie) |x Mécanismes. | |
| 650 | 6 | |a Catalyse. | |
| 650 | 6 | |a Composés organiques |x Synthèse. | |
| 650 | 7 | |a SCIENCE |x Chemistry |x Organic. |2 bisacsh | |
| 650 | 7 | |a Catalysis |2 fast | |
| 650 | 7 | |a Chemical reactions |2 fast | |
| 650 | 7 | |a Organic compounds |x Synthesis |2 fast | |
| 650 | 7 | |a Organic reaction mechanisms |2 fast | |
| 700 | 1 | |a Xu, Peng-Fei, |d 1964- |e editor. | |
| 700 | 1 | |a Wang, Wei |c (Associate professor of chemistry), |e editor. | |
| 758 | |i has work: |a Catalytic cascade reactions (Text) |1 https://id.oclc.org/worldcat/entity/E39PCFx9cMrC9YPdcGVwpQqQmd |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
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