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Chiral Lewis Acids / / edited by Koichi Mikami
| Chiral Lewis Acids / / edited by Koichi Mikami |
| Edizione | [1st ed. 2018.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2018 |
| Descrizione fisica | 1 online resource (VII, 220 p. 43 illus.) |
| Disciplina | 547.2 |
| Collana | Topics in Organometallic Chemistry |
| Soggetto topico |
Organometallic chemistry
Catalysis Chemistry, Inorganic Organometallic Chemistry Inorganic Chemistry |
| ISBN | 3-319-70806-6 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Chiral Fluorous Lewis Acid Complexes -- Chiral Lewis & Broensted Acids -- Organocatalysts combined with Chiral Lewis Acid Complexes -- Hybrid Ligands for Chiral Lewis Acids -- Chirality in Lewis Acid Complexes -- Chiral Bimetallic Lewis Acids -- Chiral Alkali Earth Complexes -- Broensted Acid/Lewis Base Hybrid Complexes -- Chiral Lewis Acids for Alder Ene & Diels-Alder reactions -- Chiral Lewis Acids in Surface -- The Future of Chiral Lewis Acids -- Carbophilic Gold Lewis Acid Complexes. |
| Record Nr. | UNINA-9910298604703321 |
| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2018 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Green reaction media in organic synthesis [[electronic resource] /] / edited by Koichi Mikami
| Green reaction media in organic synthesis [[electronic resource] /] / edited by Koichi Mikami |
| Pubbl/distr/stampa | Ames, Iowa, : Blackwell Pub., 2005 |
| Descrizione fisica | 1 online resource (202 p.) |
| Disciplina |
547.2
660.2844 660/.2844 |
| Altri autori (Persone) | MikamiKoichi |
| Soggetto topico |
Solvents - Environmental aspects
Organic compounds - Synthesis - Environmental aspects Green products |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-74856-7
9786610748563 0-470-98877-0 1-4051-7245-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Green Reaction Media in Organic Synthesis; Contents; Contributors; Preface; 1 Introduction; 1.1 Green reaction media; 1.2 Ionic liquids; 1.3 Fluorous media; 1.4 Supercritical carbon dioxide; References; 2 Ionic liquids; 2.1 Historical background and synthesis; 2.1.1 Historical background; 2.1.2 Synthesis; 2.1.2.1 Preparation of imidazolium halides; 2.1.2.2 Anion metathesis; 2.1.2.3 Functionalized imidazolium ionic liquids; 2.1.2.4 Other types of ionic liquid; 2.1.2.5 Purification; 2.2 Physical properties; 2.2.1 Melting point; 2.2.2 Thermal stability; 2.2.3 Polarity; 2.2.4 Solubility
2.2.5 Viscosity2.2.6 Acidity; 2.2.7 Chirality; 2.2.8 Toxicity and environmental issues; 2.3 Applications as reaction media; 2.3.1 Hydroformylation; 2.3.2 Hydrogenation; 2.3.3 The Friedel-Crafts reaction; 2.3.4 Epoxidation; 2.3.5 Palladium-catalyzed C-C bond formation; 2.3.5.1 The Mizoroki-Heck reaction; 2.3.5.2 The Suzuki-Miyaura cross-coupling reaction; 2.3.5.3 Other palladium-catalyzed cross-coupling reactions; 2.3.6 The Diels-Alder reaction; 2.3.7 Biocatalysis in ionic liquids; 2.4 The future of ionic liquids; 2.5 Experimental part; 2.5.1 Preparation of [bmim][Cl] 2.5.2 Preparation of [bmim][PF6]2.5.3 Preparation of a chiral imidazolium ionic liquid; 2.5.4 Enantioselective hydrogenation of methyl acetoacetate; 2.5.5 Epoxidation of 2,2-dimethylchromene; 2.5.6 Mizoroki-Heck reaction between butyl acrylate and iodobenzene under microwave irradiation; 2.5.7 Diphenylacetylene by the Sonogashira coupling reaction; References; 3 Fluorous solvents; 3.1 Historical background; 3.2 Physical properties; 3.2.1 Key design elements in fluorous/organic liquid biphasic reactions; 3.2.2 Commercial availability; 3.2.3 Polarity; 3.2.4 Solute solubilities 3.2.5 Fluorous solvent miscibilities3.2.6 Partition coefficients and fluorophilicities; 3.2.7 Toxicity and environmental issues; 3.3 Applications as reaction media; 3.3.1 Fluorous catalysts for fluorous biphasic systems; 3.3.1.1 Hydroformylation; 3.3.1.2 Hydrogenation; 3.3.1.3 Catalytic hydroboration and hydrosilylation; 3.3.1.4 Catalytic oxidation reactions; 3.3.1.5 Coupling reactions; 3.3.1.6 Fluorous acid and base catalysts; 3.3.2 Enantioselective catalysts for fluorous biphasic systems; 3.3.2.1 Reduction; 3.3.2.2 Epoxidation; 3.3.2.3 Protonation 3.3.2.4 Et2Zn or Et3Al addition to aldehydes3.3.3 Heavy fluorous reagents; 3.3.3.1 Fluorous tin hydrides; 3.3.3.2 The Stille coupling reaction; 3.3.3.3 Radical carbonylation reaction; 3.3.3.4 Fluorous tin azide; 3.3.3.5 Fluorous sulfide and sulfoxide; 3.3.3.6 Other fluorous reagents; 3.3.4 Heavy fluorous protecting groups; 3.3.4.1 Trifluoroalkylsilyl protecting group; 3.3.4.2 Fluorous alcohol protective group; 3.3.4.3 Fluorous carboxylic acid protecting group; 3.4 Light fluorous compounds and fluorous silica gel; 3.4.1 Heavy and light fluorous molecules and separation strategy 3.4.2 Solid-phase extractions with fluorous silica gel |
| Record Nr. | UNINA-9910143316403321 |
| Ames, Iowa, : Blackwell Pub., 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Green reaction media in organic synthesis [[electronic resource] /] / edited by Koichi Mikami
| Green reaction media in organic synthesis [[electronic resource] /] / edited by Koichi Mikami |
| Pubbl/distr/stampa | Ames, Iowa, : Blackwell Pub., 2005 |
| Descrizione fisica | 1 online resource (202 p.) |
| Disciplina |
547.2
660.2844 660/.2844 |
| Altri autori (Persone) | MikamiKoichi |
| Soggetto topico |
Solvents - Environmental aspects
Organic compounds - Synthesis - Environmental aspects Green products |
| ISBN |
1-280-74856-7
9786610748563 0-470-98877-0 1-4051-7245-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Green Reaction Media in Organic Synthesis; Contents; Contributors; Preface; 1 Introduction; 1.1 Green reaction media; 1.2 Ionic liquids; 1.3 Fluorous media; 1.4 Supercritical carbon dioxide; References; 2 Ionic liquids; 2.1 Historical background and synthesis; 2.1.1 Historical background; 2.1.2 Synthesis; 2.1.2.1 Preparation of imidazolium halides; 2.1.2.2 Anion metathesis; 2.1.2.3 Functionalized imidazolium ionic liquids; 2.1.2.4 Other types of ionic liquid; 2.1.2.5 Purification; 2.2 Physical properties; 2.2.1 Melting point; 2.2.2 Thermal stability; 2.2.3 Polarity; 2.2.4 Solubility
2.2.5 Viscosity2.2.6 Acidity; 2.2.7 Chirality; 2.2.8 Toxicity and environmental issues; 2.3 Applications as reaction media; 2.3.1 Hydroformylation; 2.3.2 Hydrogenation; 2.3.3 The Friedel-Crafts reaction; 2.3.4 Epoxidation; 2.3.5 Palladium-catalyzed C-C bond formation; 2.3.5.1 The Mizoroki-Heck reaction; 2.3.5.2 The Suzuki-Miyaura cross-coupling reaction; 2.3.5.3 Other palladium-catalyzed cross-coupling reactions; 2.3.6 The Diels-Alder reaction; 2.3.7 Biocatalysis in ionic liquids; 2.4 The future of ionic liquids; 2.5 Experimental part; 2.5.1 Preparation of [bmim][Cl] 2.5.2 Preparation of [bmim][PF6]2.5.3 Preparation of a chiral imidazolium ionic liquid; 2.5.4 Enantioselective hydrogenation of methyl acetoacetate; 2.5.5 Epoxidation of 2,2-dimethylchromene; 2.5.6 Mizoroki-Heck reaction between butyl acrylate and iodobenzene under microwave irradiation; 2.5.7 Diphenylacetylene by the Sonogashira coupling reaction; References; 3 Fluorous solvents; 3.1 Historical background; 3.2 Physical properties; 3.2.1 Key design elements in fluorous/organic liquid biphasic reactions; 3.2.2 Commercial availability; 3.2.3 Polarity; 3.2.4 Solute solubilities 3.2.5 Fluorous solvent miscibilities3.2.6 Partition coefficients and fluorophilicities; 3.2.7 Toxicity and environmental issues; 3.3 Applications as reaction media; 3.3.1 Fluorous catalysts for fluorous biphasic systems; 3.3.1.1 Hydroformylation; 3.3.1.2 Hydrogenation; 3.3.1.3 Catalytic hydroboration and hydrosilylation; 3.3.1.4 Catalytic oxidation reactions; 3.3.1.5 Coupling reactions; 3.3.1.6 Fluorous acid and base catalysts; 3.3.2 Enantioselective catalysts for fluorous biphasic systems; 3.3.2.1 Reduction; 3.3.2.2 Epoxidation; 3.3.2.3 Protonation 3.3.2.4 Et2Zn or Et3Al addition to aldehydes3.3.3 Heavy fluorous reagents; 3.3.3.1 Fluorous tin hydrides; 3.3.3.2 The Stille coupling reaction; 3.3.3.3 Radical carbonylation reaction; 3.3.3.4 Fluorous tin azide; 3.3.3.5 Fluorous sulfide and sulfoxide; 3.3.3.6 Other fluorous reagents; 3.3.4 Heavy fluorous protecting groups; 3.3.4.1 Trifluoroalkylsilyl protecting group; 3.3.4.2 Fluorous alcohol protective group; 3.3.4.3 Fluorous carboxylic acid protecting group; 3.4 Light fluorous compounds and fluorous silica gel; 3.4.1 Heavy and light fluorous molecules and separation strategy 3.4.2 Solid-phase extractions with fluorous silica gel |
| Record Nr. | UNISA-996213064903316 |
| Ames, Iowa, : Blackwell Pub., 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Green reaction media in organic synthesis [[electronic resource] /] / edited by Koichi Mikami
| Green reaction media in organic synthesis [[electronic resource] /] / edited by Koichi Mikami |
| Pubbl/distr/stampa | Ames, Iowa, : Blackwell Pub., 2005 |
| Descrizione fisica | 1 online resource (202 p.) |
| Disciplina |
547.2
660.2844 660/.2844 |
| Altri autori (Persone) | MikamiKoichi |
| Soggetto topico |
Solvents - Environmental aspects
Organic compounds - Synthesis - Environmental aspects Green products |
| ISBN |
1-280-74856-7
9786610748563 0-470-98877-0 1-4051-7245-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Green Reaction Media in Organic Synthesis; Contents; Contributors; Preface; 1 Introduction; 1.1 Green reaction media; 1.2 Ionic liquids; 1.3 Fluorous media; 1.4 Supercritical carbon dioxide; References; 2 Ionic liquids; 2.1 Historical background and synthesis; 2.1.1 Historical background; 2.1.2 Synthesis; 2.1.2.1 Preparation of imidazolium halides; 2.1.2.2 Anion metathesis; 2.1.2.3 Functionalized imidazolium ionic liquids; 2.1.2.4 Other types of ionic liquid; 2.1.2.5 Purification; 2.2 Physical properties; 2.2.1 Melting point; 2.2.2 Thermal stability; 2.2.3 Polarity; 2.2.4 Solubility
2.2.5 Viscosity2.2.6 Acidity; 2.2.7 Chirality; 2.2.8 Toxicity and environmental issues; 2.3 Applications as reaction media; 2.3.1 Hydroformylation; 2.3.2 Hydrogenation; 2.3.3 The Friedel-Crafts reaction; 2.3.4 Epoxidation; 2.3.5 Palladium-catalyzed C-C bond formation; 2.3.5.1 The Mizoroki-Heck reaction; 2.3.5.2 The Suzuki-Miyaura cross-coupling reaction; 2.3.5.3 Other palladium-catalyzed cross-coupling reactions; 2.3.6 The Diels-Alder reaction; 2.3.7 Biocatalysis in ionic liquids; 2.4 The future of ionic liquids; 2.5 Experimental part; 2.5.1 Preparation of [bmim][Cl] 2.5.2 Preparation of [bmim][PF6]2.5.3 Preparation of a chiral imidazolium ionic liquid; 2.5.4 Enantioselective hydrogenation of methyl acetoacetate; 2.5.5 Epoxidation of 2,2-dimethylchromene; 2.5.6 Mizoroki-Heck reaction between butyl acrylate and iodobenzene under microwave irradiation; 2.5.7 Diphenylacetylene by the Sonogashira coupling reaction; References; 3 Fluorous solvents; 3.1 Historical background; 3.2 Physical properties; 3.2.1 Key design elements in fluorous/organic liquid biphasic reactions; 3.2.2 Commercial availability; 3.2.3 Polarity; 3.2.4 Solute solubilities 3.2.5 Fluorous solvent miscibilities3.2.6 Partition coefficients and fluorophilicities; 3.2.7 Toxicity and environmental issues; 3.3 Applications as reaction media; 3.3.1 Fluorous catalysts for fluorous biphasic systems; 3.3.1.1 Hydroformylation; 3.3.1.2 Hydrogenation; 3.3.1.3 Catalytic hydroboration and hydrosilylation; 3.3.1.4 Catalytic oxidation reactions; 3.3.1.5 Coupling reactions; 3.3.1.6 Fluorous acid and base catalysts; 3.3.2 Enantioselective catalysts for fluorous biphasic systems; 3.3.2.1 Reduction; 3.3.2.2 Epoxidation; 3.3.2.3 Protonation 3.3.2.4 Et2Zn or Et3Al addition to aldehydes3.3.3 Heavy fluorous reagents; 3.3.3.1 Fluorous tin hydrides; 3.3.3.2 The Stille coupling reaction; 3.3.3.3 Radical carbonylation reaction; 3.3.3.4 Fluorous tin azide; 3.3.3.5 Fluorous sulfide and sulfoxide; 3.3.3.6 Other fluorous reagents; 3.3.4 Heavy fluorous protecting groups; 3.3.4.1 Trifluoroalkylsilyl protecting group; 3.3.4.2 Fluorous alcohol protective group; 3.3.4.3 Fluorous carboxylic acid protecting group; 3.4 Light fluorous compounds and fluorous silica gel; 3.4.1 Heavy and light fluorous molecules and separation strategy 3.4.2 Solid-phase extractions with fluorous silica gel |
| Record Nr. | UNINA-9910830948203321 |
| Ames, Iowa, : Blackwell Pub., 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Green reaction media in organic synthesis / / edited by Koichi Mikami
| Green reaction media in organic synthesis / / edited by Koichi Mikami |
| Pubbl/distr/stampa | Ames, Iowa, : Blackwell Pub., 2005 |
| Descrizione fisica | 1 online resource (202 p.) |
| Disciplina | 660/.2844 |
| Altri autori (Persone) | MikamiKoichi |
| Soggetto topico |
Solvents - Environmental aspects
Organic compounds - Synthesis - Environmental aspects Green products |
| ISBN |
1-280-74856-7
9786610748563 0-470-98877-0 1-4051-7245-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Green Reaction Media in Organic Synthesis; Contents; Contributors; Preface; 1 Introduction; 1.1 Green reaction media; 1.2 Ionic liquids; 1.3 Fluorous media; 1.4 Supercritical carbon dioxide; References; 2 Ionic liquids; 2.1 Historical background and synthesis; 2.1.1 Historical background; 2.1.2 Synthesis; 2.1.2.1 Preparation of imidazolium halides; 2.1.2.2 Anion metathesis; 2.1.2.3 Functionalized imidazolium ionic liquids; 2.1.2.4 Other types of ionic liquid; 2.1.2.5 Purification; 2.2 Physical properties; 2.2.1 Melting point; 2.2.2 Thermal stability; 2.2.3 Polarity; 2.2.4 Solubility
2.2.5 Viscosity2.2.6 Acidity; 2.2.7 Chirality; 2.2.8 Toxicity and environmental issues; 2.3 Applications as reaction media; 2.3.1 Hydroformylation; 2.3.2 Hydrogenation; 2.3.3 The Friedel-Crafts reaction; 2.3.4 Epoxidation; 2.3.5 Palladium-catalyzed C-C bond formation; 2.3.5.1 The Mizoroki-Heck reaction; 2.3.5.2 The Suzuki-Miyaura cross-coupling reaction; 2.3.5.3 Other palladium-catalyzed cross-coupling reactions; 2.3.6 The Diels-Alder reaction; 2.3.7 Biocatalysis in ionic liquids; 2.4 The future of ionic liquids; 2.5 Experimental part; 2.5.1 Preparation of [bmim][Cl] 2.5.2 Preparation of [bmim][PF6]2.5.3 Preparation of a chiral imidazolium ionic liquid; 2.5.4 Enantioselective hydrogenation of methyl acetoacetate; 2.5.5 Epoxidation of 2,2-dimethylchromene; 2.5.6 Mizoroki-Heck reaction between butyl acrylate and iodobenzene under microwave irradiation; 2.5.7 Diphenylacetylene by the Sonogashira coupling reaction; References; 3 Fluorous solvents; 3.1 Historical background; 3.2 Physical properties; 3.2.1 Key design elements in fluorous/organic liquid biphasic reactions; 3.2.2 Commercial availability; 3.2.3 Polarity; 3.2.4 Solute solubilities 3.2.5 Fluorous solvent miscibilities3.2.6 Partition coefficients and fluorophilicities; 3.2.7 Toxicity and environmental issues; 3.3 Applications as reaction media; 3.3.1 Fluorous catalysts for fluorous biphasic systems; 3.3.1.1 Hydroformylation; 3.3.1.2 Hydrogenation; 3.3.1.3 Catalytic hydroboration and hydrosilylation; 3.3.1.4 Catalytic oxidation reactions; 3.3.1.5 Coupling reactions; 3.3.1.6 Fluorous acid and base catalysts; 3.3.2 Enantioselective catalysts for fluorous biphasic systems; 3.3.2.1 Reduction; 3.3.2.2 Epoxidation; 3.3.2.3 Protonation 3.3.2.4 Et2Zn or Et3Al addition to aldehydes3.3.3 Heavy fluorous reagents; 3.3.3.1 Fluorous tin hydrides; 3.3.3.2 The Stille coupling reaction; 3.3.3.3 Radical carbonylation reaction; 3.3.3.4 Fluorous tin azide; 3.3.3.5 Fluorous sulfide and sulfoxide; 3.3.3.6 Other fluorous reagents; 3.3.4 Heavy fluorous protecting groups; 3.3.4.1 Trifluoroalkylsilyl protecting group; 3.3.4.2 Fluorous alcohol protective group; 3.3.4.3 Fluorous carboxylic acid protecting group; 3.4 Light fluorous compounds and fluorous silica gel; 3.4.1 Heavy and light fluorous molecules and separation strategy 3.4.2 Solid-phase extractions with fluorous silica gel |
| Record Nr. | UNINA-9910877880603321 |
| Ames, Iowa, : Blackwell Pub., 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
New frontiers in asymmetric catalysis / / edited by Koichi Mikami, Mark Lautens
| New frontiers in asymmetric catalysis / / edited by Koichi Mikami, Mark Lautens |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley-Interscience, c2007 |
| Descrizione fisica | 1 online resource (436 p.) |
| Disciplina | 541/.395 |
| Altri autori (Persone) |
MikamiKoichi
LautensM (Mark) |
| Soggetto topico |
Catalysis - Research
Asymmetry (Chemistry) - Research |
| ISBN |
1-280-90102-0
9786610901029 0-470-09799-X 0-470-09800-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
NEW FRONTIERS IN ASYMMETRIC CATALYSIS; CONTENTS; PREFACE; CONTRIBUTORS; 1 Ligand Design for Catalytic Asymmetric Reduction; 1.1 Introduction; 1.2 Hydrogenation of Olefins; 1.2.1 Enamide Hydrogenation with Rhodium Catalysts; 1.2.2 Hydrogenation of Functionalized Olefins with Ruthenium Catalysts; 1.2.3 Hydrogenation of Simple Olefins with Iridium Catalysts; 1.3 Reduction of Ketones; 1.3.1 Hydrogenation of Functionalized Ketones; 1.3.2 Hydrogenation of Simple Ketones; 1.3.3 Transfer Hydrogenation of Ketones; 1.3.4 Hydroboration of Ketones; 1.4 Reduction of Imines; References
2 Ligand Design for Oxidation2.1 Introduction; 2.2 Catalytic Enantioselective Epoxidation of Unfunctionalized Olefins; 2.3 Enantioselective Metal-Catalyzed Baeyer-Villiger Oxidation; 2.4 Optical Resolution during Oxidation of Alcohols; 2.5 Catalytic Enantioselective Oxidative Coupling of 2-Naphthols; 2.6 Concluding Remarks; References; 3 Ligand Design for C-C Bond Formation; 3.1 Introduction; 3.2 1,4-Addition and Related Reactions; 3.2.1 Copper Catalysis; 3.2.2 Rhodium Catalysis; 3.3 Cross-Coupling Reactions; 3.3.1 Kumada-Type Cross-Couplings; 3.3.2 Suzuki-Type Cross-Couplings; References 4 Activation of Small Molecules (C=O, HCN, RN=C, and CO(2))4.1 Introduction; 4.2 Asymmetric Hydroformylation of Olefins; 4.2.1 The Mechanism of Hydroformylation; 4.2.2 Scope and Limitation of Asymmetric Hydroformylation; 4.2.3 ''Greener'' Catalysts in Asymmetric Hydroformylation; 4.3 Asymmetric Hydrocarbohydroxylation and Related Reactions; 4.3.1 Asymmetric Hydrocarbalkoxylation of Alkenes; 4.3.2 Asymmetric Oxidative Hydrocarbalkoxylation of Alkenes; 4.3.3 Asymmetric Carbonylation of Carbon-Heteroatom Bonds; 4.4 Asymmetric Ketone Formation from Carbon-Carbon Multiple Bonds and CO 4.4.1 Asymmetric Pauson-Khand Reaction4.4.2 Asymmetric Alternating Copolymerization of Olefins with CO; 4.4.3 Asymmetric Polymerization of Isocyanide; 4.5 Asymmetric Hydrocyanation of Olefins; 4.6 Asymmetric Addition of Cyanide and Isocyanide to Aldehydes or Imines; 4.7 Asymmetric Addition of Carbon Dioxide; 4.8 Conclusion and Outlook; References; 5 Asymmetric Synthesis Based on Catalytic Activation of C-H Bonds and C-C Bonds; 5.1 Introduction; 5.2 Asymmetric Synthesis via Activation of C-H Bonds; 5.2.1 Formation of C-C Bonds; 5.2.2 Formation of C-O Bonds; 5.2.3 Formation of C-N Bonds 5.3 Asymmetric Synthesis via Activation of C-C Bonds5.3.1 Enantioselective C-C Bond Cleavage; 5.3.2 Formation of C-C Bonds; 5.3.3 Formation of C-O Bonds; 5.4 Conclusions and Outlook; Acknowledgments; References; 6 Recent Progress in the Metathesis Reaction; 6.1 Introduction; 6.2 Olefin Metathesis; 6.2.1 Ring-Closing Olefin Metathesis; 6.2.2 Cross-Metathesis (CM) of Diene; 6.2.3 Ring-Opening Metathesis (ROM)-Ring-Closing Metathesis (RCM) of Alkene; 6.2.4 Catalytic Asymmetric Olefin Metathesis; 6.3 Enyne Metathesis; 6.3.1 Ring-Closing Enyne Metathesis 6.3.2 Ring-Opening Metathesis (ROM)-Ring-Closing Metathesis (RCM) of Cycloalkene-Yne |
| Record Nr. | UNINA-9910147019003321 |
| Hoboken, N.J., : Wiley-Interscience, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||