Homo- and Heterobimetallic Complexes in Catalysis [[electronic resource] ] : Cooperative Catalysis / / edited by Philippe Kalck |
Edizione | [1st ed. 2016.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016 |
Descrizione fisica | 1 online resource (XIII, 277 p.) |
Disciplina | 541.395 |
Collana | Topics in Organometallic Chemistry |
Soggetto topico |
Organometallic chemistry
Catalysis Chemical engineering Organometallic Chemistry Industrial Chemistry/Chemical Engineering |
ISBN | 3-319-34184-7 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Bimetallic homogeneous hydroformylation -- Binuclear iridium complexes in catalysis -- Reactivity and catalysis at sites trans to the [Ru-Ru] bond -- Alkyne activation using bimetallic catalysts,- “Early-Late” heterobimetallic catalysis and beyond -- The catalytic binuclear elimination reaction: importance of non-linear kinetic effects and increased synthetic efficiency -- Biomimetic complexes for production of dihydrogen and reduction of CO2. |
Record Nr. | UNINA-9910767562303321 |
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Homogeneous Gold Catalysis [[electronic resource] /] / edited by LeGrande M. Slaughter |
Edizione | [1st ed. 2015.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 |
Descrizione fisica | 1 online resource (VII, 288 p. 315 illus., 40 illus. in color.) |
Disciplina | 547.05 |
Collana | Topics in Current Chemistry |
Soggetto topico |
Organometallic chemistry
Catalysis Chemical engineering Organometallic Chemistry Industrial Chemistry/Chemical Engineering |
ISBN | 3-319-13722-0 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Bimetallic Cooperativity in Gold Catalysis -- Gold-Catalyzed Claisen- and Cope-Type Rearrangements -- Gold-Catalyzed Carbene Mediated Reactions -- Gold-Catalyzed Tandem and Domino Reactions -- Gold p-Complexes as Model Intermediates in Gold Catalysis -- Recent Computational Insights into Gold-Catalyzed Reaction Mechanisms -- The Roles of Oxonium Chemistry and Ligand Design in Gold Catalysis -- Gold-Catalyzed Transformations of Unsaturated Alcohols. |
Record Nr. | UNINA-9910298616803321 |
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Hydrofunctionalization [[electronic resource] /] / edited by Valentine P. Ananikov, Masato Tanaka |
Edizione | [1st ed. 2013.] |
Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2013 |
Descrizione fisica | 1 online resource (XII, 368 p.) |
Disciplina | 547.05 |
Collana | Topics in Organometallic Chemistry |
Soggetto topico |
Organometallic chemistry
Catalysis Organic chemistry Organometallic Chemistry Organic Chemistry |
ISBN | 3-642-33735-X |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Valentine P. Ananikov, Irina P. Beletskaya: Alkyne and alkene insertion into metal-heteroatom and metal-hydrogen bonds – the key stages of hydrofunctionalization process -- Akihiko Ishii* and Norio Nakata: The Mechanism for Transition Metal-Catalyzed Hydrochalcogenation of Unsaturated Organic Molecules -- A. L. Reznichenko and Kai C. Hultzsch: Early Transition Metal (Group 3-5, Lanthanides and Actinides) and Main Group Metal (Group 1, 2, and 13) Catalyzed Hydroamination -- Naoko Nishina and Yoshinori Yamamoto: Late transition metal catalyzed hydroamination -- Sumod A. Pullarkat and Pak-Hing Leung: Chiral Metal Complex Promoted Asymmetric Hydrophosphinations -- Masato Tanaka: Recent Progress in Transition Metal-Catalyzed Addition Reactions of H-P(O) Compounds with Unsaturated Carbon Linkages -- Christian Bruneau: Group 8 metals-catalyzed O-H bond addition to unsaturated molecules -- Giorgio Abbiati, Egle M. Beccalli, Elisabetta Rossi: Groups 9 and 10 metals-catalyzed O-H bond addition to unsaturated molecules -- Núria Huguet and Antonio M. Echavarren: Gold-Catalyzed O-H Bond Addition to Unsaturated Organic Molecules -- Akiya Ogawa: Transition-Metal-Catalyzed S-H and Se-H Bonds Addition to Unsaturated Molecules. |
Record Nr. | UNINA-9910437801103321 |
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2013 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Insights into the Chemistry of Organic Structure-Directing Agents in the Synthesis of Zeolitic Materials [[electronic resource] /] / edited by Luis Gómez-Hortigüela |
Edizione | [1st ed. 2018.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2018 |
Descrizione fisica | 1 online resource (VII, 250 p.) |
Disciplina | 549.68 |
Collana | Structure and Bonding |
Soggetto topico |
Physical chemistry
Organometallic chemistry Inorganic chemistry Structural materials Physical Chemistry Organometallic Chemistry Inorganic Chemistry Structural Materials |
ISBN | 3-319-74289-2 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Introduction of structure-directing phenomenon by organic molecules: general aspects -- Location of organic structure-directing agents by diffraction techniques -- Molecular modelling of organic structure-direction phenomena -- Beyond nitrogen organic structure-directing agents -- Role of supramolecular chemistry during templating phenomenon in zeolite synthesis -- Metal Complexes as structure directing agents for zeolites and related microporous materials -- Chiral organic structure-directing agents. |
Record Nr. | UNINA-9910298606703321 |
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2018 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Inventing Reactions [[electronic resource] /] / edited by Lukas J. Gooßen |
Edizione | [1st ed. 2013.] |
Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2013 |
Descrizione fisica | 1 online resource (XIV, 342 p.) |
Disciplina | 547/.05045 |
Collana | Topics in Organometallic Chemistry |
Soggetto topico |
Organometallic chemistry
Catalysis Organic chemistry Organometallic Chemistry Organic Chemistry |
ISBN | 3-642-34286-8 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Barry Trost: Transition metal catalyzed allylic alkylation -- Jeffrey W. Bode: Reinventing Amide Bond Formation -- Naoto Chatani and Mamoru Tobisu: Catalytic Transformations Involving the Cleavage of C-OMe Bonds -- Gregory L. Beutner and Scott E. Denmark: The Interplay of Invention, Observation and Discovery in the Development of Lewis Base Activation of Lewis Acids for Catalytic Enantioselective Synthesis -- David R. Stuart and Keith Fagnou: The Discovery and Development of a Palladium(II)-Catalyzed Oxidative Cross-Coupling of Two Unactivated Arenes -- Lukas Gooßen and Käthe Gooßen: Decarboxylative Cross-Coupling Reactions -- A. Stephen K. Hashmi: Gold-Catalyzed Organic Reactions -- Ben List: Developing Catalytic Asymmetric Acetalizations -- Steven M. Bischof, Brian G. Hashiguchi, Michael M. Konnick, and Roy A. Periana: The De NovoDesign of CH Bond Hydroxylation Catalysts -- Benoit Cardinal-David, Karl A. Scheidt: Carbene Catalysis: Beyond the Benzoin and Stetter Reactions -- Kenso Soai and Tsuneomi Kawasaki: Asymmetric autocatalysis of pyrimidyl alkanol -- Douglas C. Behenna and Brian M. Stoltz: Natural Products as Inspiration for Reaction Development: Catalytic Enantioselective Decarboxylative Reactions of Prochiral Enolate Equivalents. Hisashi Yamamoto: Acid Catalysis in Organic Synthesis. |
Record Nr. | UNINA-9910767581003321 |
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2013 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Ionic Liquids (ILs) in Organometallic Catalysis [[electronic resource] /] / edited by Jairton Dupont, László Kollár |
Edizione | [1st ed. 2015.] |
Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2015 |
Descrizione fisica | 1 online resource (VIII, 353 p. 320 illus., 28 illus. in color.) |
Disciplina | 541.372 |
Collana | Topics in Organometallic Chemistry |
Soggetto topico |
Organometallic chemistry
Catalysis Organometallic Chemistry |
ISBN | 3-662-47857-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910768457703321 |
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2015 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Iron Catalysis II [[electronic resource] /] / edited by Eike Bauer |
Edizione | [1st ed. 2015.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 |
Descrizione fisica | 1 online resource (IX, 361 p. 515 illus., 6 illus. in color.) |
Disciplina | 669.1 |
Collana | Topics in Organometallic Chemistry |
Soggetto topico |
Organometallic chemistry
Catalysis Chemical engineering Organometallic Chemistry Industrial Chemistry/Chemical Engineering |
ISBN | 3-319-19396-1 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Intro -- Preface -- Contents -- Iron Catalysis: Historic Overview and Current Trends -- 1 Introduction -- 2 Abundance and Low Toxicity -- 3 Historic Development -- 4 Overview of Main Reactions That Are Catalyzed Under Homogeneous Conditions by Iron Complexes -- 4.1 C-C Bond-Forming Reactions -- 4.2 C-Heteroatom and Heteroatom-Heteroatom Bond-Forming Reactions -- 4.3 Oxidation Reactions -- 4.4 Reduction Reactions -- 4.5 Polymerization Reactions -- 4.6 Enantioselective Iron Catalysis and Stoichiometric Considerations -- 5 Impurities in Iron Metal as the Actual Catalyst? -- 6 Recent Heterogeneous Applications of Iron -- 7 Outlook -- References -- The Development of Iron Catalysts for Cross-Coupling Reactions -- 1 Introduction -- 1.1 Background -- 1.2 Scope -- 2 Iron Catalysts for the Cross-Coupling of Grignard Reagents -- 2.1 Oxygen, Nitrogen and Sulphur Donor Ligands -- 2.2 Phosphines and Related Ligands -- 2.3 N-Heterocyclic Carbene Ligands -- 3 Iron Catalysts for the Cross-Coupling of Softer Nucleophiles -- 3.1 Zinc-Based Nucleophiles -- 3.2 Boron-Based Nucleophiles -- 3.3 Aluminium-, Gallium-, Indium- and Thallium-Based Nucleophiles -- 4 Summary and Outlook -- References -- Iron-Catalyzed Cross-Dehydrogenative-Coupling Reactions -- 1 Introduction -- 2 Csp3-Csp3 CDC Reaction -- 3 Csp3-Csp2 CDC Reactions -- 4 Csp3-Csp CDC Reaction -- 5 Other C-C CDC Reaction -- 6 E-E CDC Reaction -- 7 Conclusion -- References -- Iron-Catalyzed Carbon-Nitrogen, Carbon-Phosphorus, and Carbon-Sulfur Bond Formation and Cyclization Reactions -- 1 Introduction -- 2 Iron-Catalyzed C-N Bond Formations -- 2.1 Cross-Coupling Reactions -- 2.2 Allylic Substitution Reactions -- 2.3 C-H Functionalization -- 2.3.1 Cross-Dehydrogenative Coupling Reactions -- 2.3.2 N-Arylation via C-H Activation -- 2.3.3 Decomposition of Azide Generation of Nitrenes.
2.4 Synthesis of Nitrogenated Heterocycles -- 2.4.1 Aziridination of Olefins -- 2.4.2 Construction of Five-Membered Cycles Containing Nitrogen Atoms -- Csp2-H or Csp3-H Functionalization Reactions -- [2+2+1]-Cycloaddition -- [3+2]-Cycloaddition Reactions -- [4+1]-Cycloaddition -- Intermolecular Aminohydroxylation of Olefins -- Hydroamination of Alkenes -- Synthesis of Indoles -- 2.4.3 Construction of Six-Membered Cycles -- Synthesis of Pyridines -- Synthesis of Tetrahydroquinolines and Dihydroquinazolines -- Synthesis of Quinolines -- 2.5 Miscellaneous -- 2.5.1 Ring Opening of Epoxides -- 2.5.2 Amide Derivative Synthesis -- 2.5.3 Synthesis of Allenyl Triazoles -- 2.5.4 Azidation of beta-Ketoesters -- 2.5.5 Rearrangement of Allyl and Propargyl Sulfides -- 2.5.6 Synthesis of Oximes -- 3 Iron-Catalyzed C-S Bond Formations -- 3.1 Michael Additions -- 3.2 Cross-Coupling Reactions -- 3.3 Addition on Alkynes -- 3.4 Allylic Substitution -- 3.5 Synthesis of Benzothiazoles -- 3.6 Miscellaneous Reactions -- 4 Iron-Catalyzed C-P Bond Formation -- 5 Conclusion -- References -- High-Valent Iron in Biomimetic Alkane Oxidation Catalysis -- 1 Iron-Based Enzymes -- 2 Metal-Ion Catalysed Autooxidation -- 3 Fenton Chemistry -- 4 Oxidation Catalysis with Synthetic Mononuclear Nonheme Fe(II) Complexes -- 4.1 Tetradentate Ligands -- 4.2 Pentadentate Ligands -- 5 Mechanistic Discussions -- 6 Summary and Conclusions -- References -- Iron-Catalyzed Reduction and Hydroelementation Reactions -- 1 Reduction of Alkynes and Alkenes -- 1.1 Hydrogenation and Transfer Hydrogenation -- 1.2 Hydrosilylation -- 2 Reduction of Aldehydes and Ketones -- 2.1 Hydrogenation Reactions -- 2.2 Transfer Hydrogenation -- 2.3 Hydrosilylation Reactions -- 3 Reduction of Imines and Nitro-derivatives and Reductive Amination of Carbonyl Compounds -- 3.1 Reduction of Imines. 3.2 Reduction of Nitrile and Nitro-compounds En Route to Primary Amines -- 3.3 Direct Reductive Amination (DRA) -- 4 Reduction of Carboxylic Acid Derivatives and Carbon Dioxide -- 4.1 Amides -- 4.2 Nitriles -- 4.3 Carboxylic Esters -- 4.4 Carboxylic Acids -- 4.5 Ureas -- 4.6 Carbon Dioxide and Formic Acid -- 5 Reduction of Sulfoxides -- 6 Hydroboration of Alkenes and Alkynes -- 7 Conclusion -- References -- Iron-Catalyzed Oligomerization and Polymerization Reactions -- 1 Introduction and Scope -- 2 Ethylene Oligomerization and Polymerization -- 2.1 Nitrogen-Based Architectures for Ligand Development -- 2.1.1 Neutral Tridentate Ligands -- 2.1.2 Neutral Bidentate Ligands -- 2.1.3 Anionic Ligands -- 2.1.4 Repeated Unit Ligands -- 2.2 Comprehension and Characterization -- 2.3 Supported Homogeneous Iron Catalysts for Oligomerization and Polymerization of Ethylene -- 2.3.1 Impregnation -- 2.3.2 Iron Catalyst Anchoring -- 2.3.3 Self-Immobilization -- 3 Multiple Single-Site Catalysis -- 3.1 Reactor Blending -- 3.2 Tandem Catalysis -- 4 Diene Polymerization -- 4.1 Iron-Based Catalysts for Polymerization of Conjugated Dienes -- 4.1.1 Bidentate Nitrogen-Based Ligands -- 4.1.2 Tridentate Nitrogen-Based Ligands -- 4.2 Iron-Based Catalysts for Homo- and Copolymerization of Olefins and Nonconjugated Dienes -- 5 Conclusion and Outlook -- References -- Enantioselective Iron Catalysts -- 1 Introduction -- 2 Chiral Iron Porphyrins -- 3 Chiral Iron Bipyridines -- 4 Chiral Schiff Base-Salen-Salan Catalysts -- 4.1 Schiff Base Catalysts -- 4.2 Salen Catalysts -- 4.3 Salan Catalysts -- 5 Bis(oxazoline) Catalysts -- 6 Pyridine bis(Oxazoline) Catalysts -- 7 Diamine-Derived Catalysts -- 8 Diphosphine-Derived Catalysts -- 9 Binaphthyl-Derived Catalysts -- 10 Planar-Chiral Ferrocenyl Catalysts -- 11 Other Catalysts -- 12 Summary and Overview -- References. Molecular Iron-Based Oxidants and Their Stoichiometric Reactions -- 1 Trends in the Use of Iron in Catalysis -- 2 Iron-Based Oxidations and Iron-Oxidant Species -- 3 Iron in Biological Oxidations -- 4 Activation of Dioxygen by Biomimetic Iron Complexes -- 4.1 Reactions of Iron(III)-Substrate Adducts with Dioxygen -- 4.2 Binding of Dioxygen to Iron(II) Complexes -- 5 Nucleophilic Reactions of Iron Peroxide Adducts -- 5.1 Reactions with Aldehydes -- 5.2 Hydroxylation of Alkanes and Aromatic Compounds -- 6 Electrophilic Reactions of Iron-Oxo Intermediates -- 6.1 High-Valent Nonheme Iron(IV)-Oxo Complexes -- 6.2 Iron(V)Oxo and Iron(IV)Oxo-(Oxidized Radical Ligand) Complexes -- 7 Halogenation Reactions of Iron-Halide and Iron-Hypohalide Adducts -- 8 Electrophilic Reactions of Iron-Nitrido and Iron-Imido Intermediates -- 9 Intramolecular Ligand Oxidations -- 10 Conclusions and Outlook -- References -- Index. |
Record Nr. | UNINA-9910768456503321 |
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2015 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Iron-Catalysed Hydrofunctionalisation of Alkenes and Alkynes [[electronic resource] /] / by Mark Greenhalgh |
Autore | Greenhalgh Mark |
Edizione | [1st ed. 2016.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016 |
Descrizione fisica | 1 online resource (319 p.) |
Disciplina | 547.412 |
Collana | Springer Theses, Recognizing Outstanding Ph.D. Research |
Soggetto topico |
Organometallic chemistry
Catalysis Chemical engineering Organometallic Chemistry Industrial Chemistry/Chemical Engineering |
ISBN | 3-319-33663-0 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Introduction -- Iron-Catalysed Hydrosilylation of Alkenes and Alkynes -- Iron-Catalysed Hydroboration of Alkenes and Alkynes -- Iron-Catalysed Hydromagnesiation of Styrene Derivatives -- Experimental -- References. |
Record Nr. | UNINA-9910254028003321 |
Greenhalgh Mark | ||
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Iron-Catalyzed Synthesis of Fused Aromatic Compounds via C–H Bond Activation [[electronic resource] /] / by Arimasa Matsumoto |
Autore | Matsumoto Arimasa |
Edizione | [1st ed. 2014.] |
Pubbl/distr/stampa | Tokyo : , : Springer Japan : , : Imprint : Springer, , 2014 |
Descrizione fisica | 1 online resource (84 p.) |
Disciplina | 541.395 |
Collana | Springer Theses, Recognizing Outstanding Ph.D. Research |
Soggetto topico |
Organometallic chemistry
Metals Organometallic Chemistry Metallic Materials |
ISBN | 4-431-54928-5 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | General Introduction -- Iron-Catalyzed Naphthalene Synthesis from Alkyne and Grignard Reagent -- Iron-Catalyzed Phenanthrene Synthesis from Alkyne and Grignard Reagent -- Iron-Catalyzed Phenanthrene Synthesis from Alkyne and Aryl Bromide Mediated by Metallic Magnesium -- Summary and Perspectives. |
Record Nr. | UNINA-9910298657403321 |
Matsumoto Arimasa | ||
Tokyo : , : Springer Japan : , : Imprint : Springer, , 2014 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Katalytische Metathese von Alkinen [[electronic resource] ] : Entwicklung neuer Katalysatoren / / von Henrike Ehrhorn |
Autore | Ehrhorn Henrike |
Edizione | [1st ed. 2017.] |
Pubbl/distr/stampa | Wiesbaden : , : Springer Fachmedien Wiesbaden : , : Imprint : Springer Spektrum, , 2017 |
Descrizione fisica | 1 online resource (X, 70 S. 12 Abb.) |
Disciplina | 546 |
Collana | BestMasters |
Soggetto topico |
Inorganic chemistry
Organometallic chemistry Catalysis Inorganic Chemistry Organometallic Chemistry |
ISBN | 3-658-17243-6 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | ger |
Nota di contenuto | Grundlagen der Metathese, Entwicklung der Alkinmetathese und Anwendung -- Molybdän(2,4,6-triisopropyl)-, Molybdän(2,4,6-tri-tert-butyl)- und Molybdän(2,4,6-trimethyl)-benzylidin-Komplexe -- Metathesen und Produktcharakterisierung. |
Record Nr. | UNINA-9910163146003321 |
Ehrhorn Henrike | ||
Wiesbaden : , : Springer Fachmedien Wiesbaden : , : Imprint : Springer Spektrum, , 2017 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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