Alkynes in Cycloadditions
John Wiley & Sons Inc (Hersteller)
9781118709313 (ISBN)
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* New achievements in classical cycloaddition reactions such as the Diels-Alder condensation with acetylenic dienophiles and [2+2] cycloadditions with acetylene components Alkynes in Cycloadditions presents a comprehensive summary of the literature on methods for the synthesis of ring systems from acetylenes for academic researchers working in the fields of organic synthesis, physical organic chemistry, organometallic chemistry, catalysis, materials science, nanomaterials and biochemistry.
Professor Irina A. Maretina, St Petersburg State Institute of Technology, St. Petersburg, Russia. Irina Maretrina is a well-known name in the field of acetylene chemistry. Her research focuses on the chemistry of alkynes, in particular diacetylenes and the synthesis and reactivity of unsaturated heteroatomic compounds, including nitrogen-containing heterocyclic compounds. Professor Boris I. Ionin (Translator), St Petersburg State Institute of Technology, Department of Organic Chemistry, St Petersburg, Russia. Boris Ionin is a renowned organic chemist specializing in acetylene and phosphorus chemistry, and nuclear magnetic resonance. He is an Editorial Board member for the Russian Journal of General Chemistry and Editor for the English translation of this journal. John C. Tebby (Consulting Editor), Emeritus Professor FRSC DSc, former Head of Chemistry, Staffordshire University.
Preface xi Acknowledgment xiii Biography xv 1 Introduction 1 2 Regioselective Syntheses of Polysubstituted Benzenes Catalyzed by Transition Metal Complexes 5 2.1 Reactions of [2+2+2] Cycloaddition of Acetylene Units 5 2.2 Stereochemical Aspect of The Problem of Intermolecular Reactions of Diynes with Monoalkynes 18 2.3 Heteroatom Bound to the Triple Bond 28 2.4 Heterohelicens. Asymmetric Syntheses 34 2.5 Aromatic Rings with Boron and Silicon Substituents 38 2.6 [2+2+2] Cycloaddition Reactions of 1-Alkynylphosphines and Their Derivatives 40 2.7 Intramolecular [2+2+2] Cycloaddition of Diynes to Alkenes 45 2.8 Polysubstituted Benzenes. Reactions of [4+2] Cycloaddition and Other Approaches 53 2.9 Combined Reactions 63 2.10 Construction of Polycyclic Systems 71 3 Radical Cycloaromatization of Systems Containing (Z)-3-hexene-1,5-diynes and (Z)-1,2,4-heptatrien-6-ynes and Related Heteroatomic Blocks 107 3.1 The Historical Aspect of the Chemistry of Enediynes, Enyne-Allenes and Enyne-Cumulenes 107 3.2 Routes to the Cycloaromatization of Enediyne and Enyne-Allene Systems. Bergman and Myers Saito Cyclization 113 3.3 Cycloaromatization by C1 C5, C2 C7 and C2 C6 (Myers Saito and Schmittel) Routes to Indeno-Fused Structures 135 3.4 External Initiation of the Enediyne Cycloaromatization 157 3.5 Features of Cycloaromatization of Heteroatomic Enediynes 179 3.6 Cycloaromatization of Hetero-Systems 223 4 Selected Cycloaddition and Heterocyclization Reactions with Unusual Acetylenic and Allenic Starting Compounds 233 4.1 Cycloaddition and Heterocyclization Reactions of Acetylenic Compounds with Electron-Withdrawing Substituents 233 4.2 Diels Alder [4+2] Cycloaddition: Acetylenes as Dienophiles 235 4.3 Formation of Cyclobutene Derivatives by [2+2]-Cycloaddition 237 4.4 [2+2] Cyclization of Some 1,3-Butadienes Produced from Acetylenic Alcohols of Propargyl Type 243 4.5 Heterocyclization of Electron-Deficient Acetylenes with Nucleophilic Reagents 245 5 Concluding Remarks 249 Index
| Mitarbeit |
Berater: John C. Tebby |
|---|---|
| Übersetzer | Boris I. Ionin |
| Verlagsort | New York |
| Sprache | englisch |
| Maße | 152 x 229 mm |
| Gewicht | 666 g |
| Themenwelt | Naturwissenschaften ► Chemie ► Organische Chemie |
| Naturwissenschaften ► Chemie ► Technische Chemie | |
| Technik ► Maschinenbau | |
| ISBN-13 | 9781118709313 / 9781118709313 |
| Zustand | Neuware |
| Informationen gemäß Produktsicherheitsverordnung (GPSR) | |
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