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Chiral ferrocenes in asymmetric catalysis
Chiral ferrocenes in asymmetric catalysis
Autore Dai Li-xin
Pubbl/distr/stampa [Place of publication not identified], : Wiley VCH, 2010
Disciplina 547.05621
Soggetto topico Ferrocene
Chirality
Catalysis
Asymmetry (Chemistry)
Chemistry
Physical Sciences & Mathematics
Organic Chemistry
ISBN 3-527-62884-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910140166403321
Dai Li-xin  
[Place of publication not identified], : Wiley VCH, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chiral ferrocenes in asymmetric catalysis
Chiral ferrocenes in asymmetric catalysis
Autore Dai Li-xin
Pubbl/distr/stampa [Place of publication not identified], : Wiley VCH, 2010
Disciplina 547.05621
Soggetto topico Ferrocene
Chirality
Catalysis
Asymmetry (Chemistry)
Chemistry
Physical Sciences & Mathematics
Organic Chemistry
ISBN 3-527-62884-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910830974903321
Dai Li-xin  
[Place of publication not identified], : Wiley VCH, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chiral ferrocenes in asymmetric catalysis
Chiral ferrocenes in asymmetric catalysis
Autore Dai Li-xin
Pubbl/distr/stampa [Place of publication not identified], : Wiley VCH, 2010
Disciplina 547.05621
Soggetto topico Ferrocene
Chirality
Catalysis
Asymmetry (Chemistry)
Chemistry
Physical Sciences & Mathematics
Organic Chemistry
ISBN 3-527-62884-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9911020237903321
Dai Li-xin  
[Place of publication not identified], : Wiley VCH, 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Ferrocenes [[electronic resource] ] : compounds, properties and applications / / Elisabeth S. Phillips, editor
Ferrocenes [[electronic resource] ] : compounds, properties and applications / / Elisabeth S. Phillips, editor
Pubbl/distr/stampa New York, : Nova Science Publishers, c2011
Descrizione fisica 1 online resource (413 p.)
Disciplina 547/.05621
Altri autori (Persone) PhillipsElisabeth S
Collana Chemical engineering methods and technology
Soggetto topico Ferrocene
Organoiron compounds
Soggetto genere / forma Electronic books.
ISBN 1-61122-224-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto ""FERROCENES: COMPOUNDS, PROPERTIES AND APPLICATIONS ""; ""FERROCENES: COMPOUNDS, PROPERTIES AND APPLICATIONS""; ""CONTENTS""; ""PREFACE""; ""SYNTHESIS OF PRISTINE AND DOPED CARBON NANOTUBES USING FERROCENE""; ""ABSTRACT ""; ""INTRODUCTION ""; ""STRUCTURE AND PROPERTIES OF FERROCENE ""; ""STRUCTURE AND BONDING ""; ""SYNTHESIS OF PRISTINE CARBON NANOTUBES ""; ""SYNTHESIS OF DOPED CARBON NANOTUBES""; ""CONCLUSION ""; ""REFERENCES ""; ""USE OF FERROCENE AND FERROCENE ADMIXED PRECURSORS FOR THE SYNTHESIS OF CARBON NANOTUBES""; ""ABSTRACT ""; ""1. INTRODUCTION""
""2. SYNTHESIS OF CNTS USING FERROCENE """"3. SYNTHESIS OF CNTS BY FERROCENE AND HYDROCARBON MIXTURE ""; ""3.1. Synthesis of CNTs by Ferrocene and Gaseous Hydrocarbon""; ""3.2. Synthesis of CNTs by Ferrocene and Liquid Hydrocarbon ""; ""3.2.1. CVD of Ferrocene - Liquid Hydrocarbon Through Syringe Pump""; ""3. 2.2. Spray Assisted CVD Method ""; ""3.2.3. Aerosol and Nebulized Spray Assisted CVD Method""; ""4. SYNTHESIS OF CNTS USING FERROCENE AND NATURAL PRECURSOR""; ""5. SYNTHESIS OF CNTS USING FERROCENE AND OTHER CARBON SOURCES""; ""6. SUMMARY ""; ""ACKNOWLEDGMENTS ""; ""REFERENCES ""
""TRANSITION-METAL CATALYZED REACTIONS IN THE SYNTHESIS OF FERROCENE DERIVATIVES""""ABSTRACT ""; ""1. INTRODUCTION ""; ""2. HOMOGENEOUS CATALYTIC HYDROGENATION OF FERROCENE DERIVATIVES ""; ""3. SYNTHESIS OF CHIRAL DIOLS BY ASYMMETRIC DIHYDROXYLATION OF FERROCENYL ALKENES ""; ""4. HOMOGENEOUS CATALYTIC HYDROSILYLATION OF FERROCENE DERIVATIVES ""; ""5. CARBON-CARBON BOND-FORMING REACTIONS ""; ""5.1. Heck Reactions of Ferrocenyl Substrates ""; ""5.2. Cross-Coupling Reactions ""; ""5.2.1. Stille Coupling ""; ""5.2.2. Suzuki Coupling ""; ""5.2.3. Negishi Coupling ""
""5.2.4. Cross-Coupling of Organomercurials """"5.2.5. Other Coupling Reactions with Organometallic Reagents""; ""5.2.6. Sonogashira Coupling ""; ""5.3. Metathesis Reactions ""; ""5.3.1. Ring-Closing Metathesis Reactions ""; ""5.3.2. Ring-Opening Metathesis Polymerization ""; ""6. C-HETEROATOM COUPLING REACTIONS OF FERROCENE DERIVATIVES ""; ""7. RING-OPENING POLYMERIZATION REACTIONS ""; ""8. COPPER CATALYZED AZIDE-ALKYNE CYCLOADDITION ""; ""9. CARBONYLATION REACTIONS LEADING TO CARBOXYLIC ACID DERIVATIVES AND CARBONYL COMPOUNDS ""; ""9.1. Palladium-Catalyzed Aminocarbonylation ""
""9.2. Carbonylative Coupling Reactions """"10. MISCELLANEOUS REACTIONS ""; ""CONCLUSION ""; ""REFERENCES ""; ""EXPLOITING FERROCENE TO DEVELOP SYNTHETIC MOLECULAR MACHINES ""; ""ABSTRACT ""; ""1. INTRODUCTION""; ""2. FERROCENE HOST-GUEST CHEMISTRY AND STIMULI RESPONSIVE HOST-GUEST SYSTEMS ""; ""2.1. Ferrocene Host-Guest Chemistry ""; ""2.2 Stimuli Responsive Host-Guest Systems Containing Ferrocene""; ""3. STIMULI RESPONSIVE INTERLOCKED ARCHITECTURES CONTAINING FERROCENE ""; ""3.1. Introduction to Mechanically Interlocked Architectures ""
""3.2 Ferrocene Containing Mechanically Interlocked Architectures""
Record Nr. UNINA-9910461206703321
New York, : Nova Science Publishers, c2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Ferrocenes [[electronic resource] ] : compounds, properties and applications / / Elisabeth S. Phillips, editor
Ferrocenes [[electronic resource] ] : compounds, properties and applications / / Elisabeth S. Phillips, editor
Pubbl/distr/stampa New York, : Nova Science Publishers, c2011
Descrizione fisica 1 online resource (413 p.)
Disciplina 547/.05621
Altri autori (Persone) PhillipsElisabeth S
Collana Chemical engineering methods and technology
Soggetto topico Ferrocene
Organoiron compounds
ISBN 1-61122-224-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto ""FERROCENES: COMPOUNDS, PROPERTIES AND APPLICATIONS ""; ""FERROCENES: COMPOUNDS, PROPERTIES AND APPLICATIONS""; ""CONTENTS""; ""PREFACE""; ""SYNTHESIS OF PRISTINE AND DOPED CARBON NANOTUBES USING FERROCENE""; ""ABSTRACT ""; ""INTRODUCTION ""; ""STRUCTURE AND PROPERTIES OF FERROCENE ""; ""STRUCTURE AND BONDING ""; ""SYNTHESIS OF PRISTINE CARBON NANOTUBES ""; ""SYNTHESIS OF DOPED CARBON NANOTUBES""; ""CONCLUSION ""; ""REFERENCES ""; ""USE OF FERROCENE AND FERROCENE ADMIXED PRECURSORS FOR THE SYNTHESIS OF CARBON NANOTUBES""; ""ABSTRACT ""; ""1. INTRODUCTION""
""2. SYNTHESIS OF CNTS USING FERROCENE """"3. SYNTHESIS OF CNTS BY FERROCENE AND HYDROCARBON MIXTURE ""; ""3.1. Synthesis of CNTs by Ferrocene and Gaseous Hydrocarbon""; ""3.2. Synthesis of CNTs by Ferrocene and Liquid Hydrocarbon ""; ""3.2.1. CVD of Ferrocene - Liquid Hydrocarbon Through Syringe Pump""; ""3. 2.2. Spray Assisted CVD Method ""; ""3.2.3. Aerosol and Nebulized Spray Assisted CVD Method""; ""4. SYNTHESIS OF CNTS USING FERROCENE AND NATURAL PRECURSOR""; ""5. SYNTHESIS OF CNTS USING FERROCENE AND OTHER CARBON SOURCES""; ""6. SUMMARY ""; ""ACKNOWLEDGMENTS ""; ""REFERENCES ""
""TRANSITION-METAL CATALYZED REACTIONS IN THE SYNTHESIS OF FERROCENE DERIVATIVES""""ABSTRACT ""; ""1. INTRODUCTION ""; ""2. HOMOGENEOUS CATALYTIC HYDROGENATION OF FERROCENE DERIVATIVES ""; ""3. SYNTHESIS OF CHIRAL DIOLS BY ASYMMETRIC DIHYDROXYLATION OF FERROCENYL ALKENES ""; ""4. HOMOGENEOUS CATALYTIC HYDROSILYLATION OF FERROCENE DERIVATIVES ""; ""5. CARBON-CARBON BOND-FORMING REACTIONS ""; ""5.1. Heck Reactions of Ferrocenyl Substrates ""; ""5.2. Cross-Coupling Reactions ""; ""5.2.1. Stille Coupling ""; ""5.2.2. Suzuki Coupling ""; ""5.2.3. Negishi Coupling ""
""5.2.4. Cross-Coupling of Organomercurials """"5.2.5. Other Coupling Reactions with Organometallic Reagents""; ""5.2.6. Sonogashira Coupling ""; ""5.3. Metathesis Reactions ""; ""5.3.1. Ring-Closing Metathesis Reactions ""; ""5.3.2. Ring-Opening Metathesis Polymerization ""; ""6. C-HETEROATOM COUPLING REACTIONS OF FERROCENE DERIVATIVES ""; ""7. RING-OPENING POLYMERIZATION REACTIONS ""; ""8. COPPER CATALYZED AZIDE-ALKYNE CYCLOADDITION ""; ""9. CARBONYLATION REACTIONS LEADING TO CARBOXYLIC ACID DERIVATIVES AND CARBONYL COMPOUNDS ""; ""9.1. Palladium-Catalyzed Aminocarbonylation ""
""9.2. Carbonylative Coupling Reactions """"10. MISCELLANEOUS REACTIONS ""; ""CONCLUSION ""; ""REFERENCES ""; ""EXPLOITING FERROCENE TO DEVELOP SYNTHETIC MOLECULAR MACHINES ""; ""ABSTRACT ""; ""1. INTRODUCTION""; ""2. FERROCENE HOST-GUEST CHEMISTRY AND STIMULI RESPONSIVE HOST-GUEST SYSTEMS ""; ""2.1. Ferrocene Host-Guest Chemistry ""; ""2.2 Stimuli Responsive Host-Guest Systems Containing Ferrocene""; ""3. STIMULI RESPONSIVE INTERLOCKED ARCHITECTURES CONTAINING FERROCENE ""; ""3.1. Introduction to Mechanically Interlocked Architectures ""
""3.2 Ferrocene Containing Mechanically Interlocked Architectures""
Record Nr. UNINA-9910790033003321
New York, : Nova Science Publishers, c2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Ferrocenes : compounds, properties and applications / / Elisabeth S. Phillips, editor
Ferrocenes : compounds, properties and applications / / Elisabeth S. Phillips, editor
Edizione [1st ed.]
Pubbl/distr/stampa New York, : Nova Science Publishers, c2011
Descrizione fisica 1 online resource (413 p.)
Disciplina 547/.05621
Altri autori (Persone) PhillipsElisabeth S
Collana Chemical engineering methods and technology
Soggetto topico Ferrocene
Organoiron compounds
ISBN 1-61122-224-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto ""FERROCENES: COMPOUNDS, PROPERTIES AND APPLICATIONS ""; ""FERROCENES: COMPOUNDS, PROPERTIES AND APPLICATIONS""; ""CONTENTS""; ""PREFACE""; ""SYNTHESIS OF PRISTINE AND DOPED CARBON NANOTUBES USING FERROCENE""; ""ABSTRACT ""; ""INTRODUCTION ""; ""STRUCTURE AND PROPERTIES OF FERROCENE ""; ""STRUCTURE AND BONDING ""; ""SYNTHESIS OF PRISTINE CARBON NANOTUBES ""; ""SYNTHESIS OF DOPED CARBON NANOTUBES""; ""CONCLUSION ""; ""REFERENCES ""; ""USE OF FERROCENE AND FERROCENE ADMIXED PRECURSORS FOR THE SYNTHESIS OF CARBON NANOTUBES""; ""ABSTRACT ""; ""1. INTRODUCTION""
""2. SYNTHESIS OF CNTS USING FERROCENE """"3. SYNTHESIS OF CNTS BY FERROCENE AND HYDROCARBON MIXTURE ""; ""3.1. Synthesis of CNTs by Ferrocene and Gaseous Hydrocarbon""; ""3.2. Synthesis of CNTs by Ferrocene and Liquid Hydrocarbon ""; ""3.2.1. CVD of Ferrocene - Liquid Hydrocarbon Through Syringe Pump""; ""3. 2.2. Spray Assisted CVD Method ""; ""3.2.3. Aerosol and Nebulized Spray Assisted CVD Method""; ""4. SYNTHESIS OF CNTS USING FERROCENE AND NATURAL PRECURSOR""; ""5. SYNTHESIS OF CNTS USING FERROCENE AND OTHER CARBON SOURCES""; ""6. SUMMARY ""; ""ACKNOWLEDGMENTS ""; ""REFERENCES ""
""TRANSITION-METAL CATALYZED REACTIONS IN THE SYNTHESIS OF FERROCENE DERIVATIVES""""ABSTRACT ""; ""1. INTRODUCTION ""; ""2. HOMOGENEOUS CATALYTIC HYDROGENATION OF FERROCENE DERIVATIVES ""; ""3. SYNTHESIS OF CHIRAL DIOLS BY ASYMMETRIC DIHYDROXYLATION OF FERROCENYL ALKENES ""; ""4. HOMOGENEOUS CATALYTIC HYDROSILYLATION OF FERROCENE DERIVATIVES ""; ""5. CARBON-CARBON BOND-FORMING REACTIONS ""; ""5.1. Heck Reactions of Ferrocenyl Substrates ""; ""5.2. Cross-Coupling Reactions ""; ""5.2.1. Stille Coupling ""; ""5.2.2. Suzuki Coupling ""; ""5.2.3. Negishi Coupling ""
""5.2.4. Cross-Coupling of Organomercurials """"5.2.5. Other Coupling Reactions with Organometallic Reagents""; ""5.2.6. Sonogashira Coupling ""; ""5.3. Metathesis Reactions ""; ""5.3.1. Ring-Closing Metathesis Reactions ""; ""5.3.2. Ring-Opening Metathesis Polymerization ""; ""6. C-HETEROATOM COUPLING REACTIONS OF FERROCENE DERIVATIVES ""; ""7. RING-OPENING POLYMERIZATION REACTIONS ""; ""8. COPPER CATALYZED AZIDE-ALKYNE CYCLOADDITION ""; ""9. CARBONYLATION REACTIONS LEADING TO CARBOXYLIC ACID DERIVATIVES AND CARBONYL COMPOUNDS ""; ""9.1. Palladium-Catalyzed Aminocarbonylation ""
""9.2. Carbonylative Coupling Reactions """"10. MISCELLANEOUS REACTIONS ""; ""CONCLUSION ""; ""REFERENCES ""; ""EXPLOITING FERROCENE TO DEVELOP SYNTHETIC MOLECULAR MACHINES ""; ""ABSTRACT ""; ""1. INTRODUCTION""; ""2. FERROCENE HOST-GUEST CHEMISTRY AND STIMULI RESPONSIVE HOST-GUEST SYSTEMS ""; ""2.1. Ferrocene Host-Guest Chemistry ""; ""2.2 Stimuli Responsive Host-Guest Systems Containing Ferrocene""; ""3. STIMULI RESPONSIVE INTERLOCKED ARCHITECTURES CONTAINING FERROCENE ""; ""3.1. Introduction to Mechanically Interlocked Architectures ""
""3.2 Ferrocene Containing Mechanically Interlocked Architectures""
Record Nr. UNINA-9910970896503321
New York, : Nova Science Publishers, c2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Ferrocenes [[electronic resource] ] : ligands, materials and biomolecules / / editor, Petr Štěpnička
Ferrocenes [[electronic resource] ] : ligands, materials and biomolecules / / editor, Petr Štěpnička
Pubbl/distr/stampa Chichester, England ; ; Hoboken, NJ, : J.Wiley, c2008
Descrizione fisica 1 online resource (669 p.)
Disciplina 547
547.05621
547/.05621
Altri autori (Persone) ŠtěpničkaPetr
Soggetto topico Ferrocene
Ligands
Biomolecules
ISBN 1-281-31984-8
9786611319847
0-470-98566-6
0-470-98565-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Ferrocenes; Contents; Preface; Contributors; PART I FERROCENE LIGANDS; 1 Monodentate Ferrocene Donor Ligands; 2 The Coordination and Homogeneous Catalytic Chemistry of 1,1 -Bis(diphenylphosphino)ferrocene and its Chalcogenide Derivatives; 3 Synthesis, Coordination Chemistry and Catalytic Use of dppf Analogs; 4 Other Symmetric 1,1 -Bidentate Ferrocene Ligands; 5 1 -Functionalised Ferrocene Phosphines: Synthesis, Coordination Chemistry and Catalytic Applications; 6 Chiral 1,2-Disubstituted Ferrocene Diphosphines for Asymmetric Catalysis
7 Synthesis and Catalytic Use of Planar Chiral and Polydentate Ferrocene DonorsPART II MATERIALS, MOLECULAR DEVICES AND BIOMOLECULES; 8 Ferrocene Sensors; 9 Ferrocene-Based Electro-Optical Materials; 10 Ferrocene-Containing Polymers and Dendrimers; 11 Ferrocene-Containing Thermotropic Liquid Crystals; 12 Crystal Engineering with Ferrocene Compounds; 13 The Bioorganometallic Chemistry of Ferrocene; Index
Record Nr. UNINA-9910145421803321
Chichester, England ; ; Hoboken, NJ, : J.Wiley, c2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Ferrocenes : ligands, materials and biomolecules / / editor, Petr Stepnicka
Ferrocenes : ligands, materials and biomolecules / / editor, Petr Stepnicka
Edizione [1st ed.]
Pubbl/distr/stampa Chichester, England ; ; Hoboken, NJ, : J.Wiley, c2008
Descrizione fisica 1 online resource (669 p.)
Disciplina 547
547.05621
547/.05621
Altri autori (Persone) ŠtěpničkaPetr
Soggetto topico Ferrocene
Ligands
Biomolecules
ISBN 9786611319847
9781281319845
1281319848
9780470985663
0470985666
9780470985656
0470985658
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Ferrocenes; Contents; Preface; Contributors; PART I FERROCENE LIGANDS; 1 Monodentate Ferrocene Donor Ligands; 2 The Coordination and Homogeneous Catalytic Chemistry of 1,1 -Bis(diphenylphosphino)ferrocene and its Chalcogenide Derivatives; 3 Synthesis, Coordination Chemistry and Catalytic Use of dppf Analogs; 4 Other Symmetric 1,1 -Bidentate Ferrocene Ligands; 5 1 -Functionalised Ferrocene Phosphines: Synthesis, Coordination Chemistry and Catalytic Applications; 6 Chiral 1,2-Disubstituted Ferrocene Diphosphines for Asymmetric Catalysis
7 Synthesis and Catalytic Use of Planar Chiral and Polydentate Ferrocene DonorsPART II MATERIALS, MOLECULAR DEVICES AND BIOMOLECULES; 8 Ferrocene Sensors; 9 Ferrocene-Based Electro-Optical Materials; 10 Ferrocene-Containing Polymers and Dendrimers; 11 Ferrocene-Containing Thermotropic Liquid Crystals; 12 Crystal Engineering with Ferrocene Compounds; 13 The Bioorganometallic Chemistry of Ferrocene; Index
Record Nr. UNINA-9910821787503321
Chichester, England ; ; Hoboken, NJ, : J.Wiley, c2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Ferrocenes [[electronic resource] ] : homogeneous catalysis, organic synthesis, materials science / / edited by Antonio Togni and Tamio Hayashi
Ferrocenes [[electronic resource] ] : homogeneous catalysis, organic synthesis, materials science / / edited by Antonio Togni and Tamio Hayashi
Pubbl/distr/stampa Weinheim ; ; New York, : VCH Publishers, c1995
Descrizione fisica 1 online resource (562 p.)
Disciplina 547.05621
Altri autori (Persone) TogniAntonio
HayashiTamio
Soggetto topico Ferrocene
Organoiron compounds
Soggetto genere / forma Electronic books.
ISBN 1-281-75871-X
9786611758714
3-527-61559-8
3-527-61558-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Ferrocenes; Preface; Contents; List of Contributors; List of Abbreviations; Part 1. Homogeneous Catalysis; 1 1,1'-Bis (dipheny1phosphino)ferrocene - Coordination Chemistry, Organic Syntheses, and Catalysis; 1.1 Introduction; 1.2 Preparation and Complexation; 1.3 Structural Properties; 1.3.1 Modes of Coordination; 1.3.2 Geometrical Distortions; 1.4 Spectroscopic Characteristics; 1.4.1 Techniques; 1.4.1.1 31P NMR Spectroscopy; 1.4.1.2 1H NMR Spectroscopy; 1.4.1.3 Mössbauer Spectroscopy; 1.4.2 NMR Fluxionality; 1.5 Catalysis; 1.5.1 Cross Coupling
1.5.1.1 Organic Electrophile and Organometallic Coupling1.5.1.2 Arylation and Vinylation of Alkenes; 1.5.1.3 Carbonylation and Carbonylative Coupling; 1.5.1.4 Nucleophilic Substitution; 1.5.1.5 Polycondensation and Polymerization; 1.5.2 Olefin Functionalization; 1.5.2.1 Hydroformylation; 1.5.2.2 Hydrogenation and Reduction; 1.5.2.3 Hydroboration and Hydrosilylation; 1.5.2.4 Isomerization; 1.6 Cluster Complexes; 1.7 Electrochemistry; 1.8 Biomedical Applications; 1.9 Summary; References; 2 Asymmetric Catalysis with Chiral Ferrocenylphosphine Ligands; 2.1 Introduction
2.2 Preparation of Chiral Ferrocenylphosphines2.3 Structure of Chiral Ferrocenylphosphines and their Transition-Metal Complexes; 2.4 Catalytic Asymmetric Reactions with Chiral Ferrocenylphosphine Ligands; 2.4.1 Cross-Coupling of Organometallics with Halides; 2.4.2 Allylic Substitution Reactions via π-Ally1 Complexes; 2.4.3 Hydrogenation of Olefins and Ketones; 2.4.4 Hydrosilylation of Olefins and Ketones; 2.4.5 Aldol Reaction of α-Isocyanocarboxylates; 2.4.6 Others; References; 3 Enantioselective Addition of Dialkylzinc to Aldehydes Catalyzed by Chiral Ferrocenyl Aminoalcohols
3.1 Introduction3.2 Chiral Ferrocenylzincs Bearing an Aminoethanol Auxiliary [12]; 3.2.1 Synthesis of the Catalysts; 3.2.2 Addition of Diethylzinc to Benzaldehyde; 3.3 N- (1-Ferrocenylalky1)-N-alk ylnorephedrines [13]; 3.3.1 Synthesis of the Catalysts; 3.3.2 Addition of Diethylzinc to Aldehydes; 3.4 Chiral Polymers Bearing N-Ferrocenylmethylephedrine [14]; 3.4.1 Synthesis of the Catalysts; 3.4.2 Addition of Diethylzinc to Benzaldehyde; 3.5 Chiral 1,2-Disubstituted Ferrocenyl Aminoalcohols [15]; 3.5.1 Synthesis of the Catalysts; 3.5.2 Addition of Dialkylzinc to Aldehydes
3.5.3 Addition of Dialkylzincs to o-Phthalaldehyde: A Facile Synthesis of Optically Active 3-Alkylphthalides [16]3.5.4 Enantio- and Diastereoselective Addition of Diethylzinc to Racemic α-Thio- and α-Selenoaldehydes [17]; 3.6 Summary; References; Part 2. Organic Synthesis - Selected Aspects; 4 Chiral Ferrocene Derivatives. An Introduction; 4.1 Central and Planar Chirality in Metallocenes; 4.2 a-Ferrocenylalkyl Carbocations; 4.2.1 Structure and Stability; 4.2.2 Stereochemistry; 4.3 Central Chiral Ferrocene Derivatives; 4.3.1 Syntheses; 4.3.1.1 By Resolution; 4.3.1.2 By Asymmetric Synthesis
4.3.1.3 From the Chiral Pool
Record Nr. UNINA-9910144280003321
Weinheim ; ; New York, : VCH Publishers, c1995
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Ferrocenes [[electronic resource] ] : homogeneous catalysis, organic synthesis, materials science / / edited by Antonio Togni and Tamio Hayashi
Ferrocenes [[electronic resource] ] : homogeneous catalysis, organic synthesis, materials science / / edited by Antonio Togni and Tamio Hayashi
Pubbl/distr/stampa Weinheim ; ; New York, : VCH Publishers, c1995
Descrizione fisica 1 online resource (562 p.)
Disciplina 547.05621
Altri autori (Persone) TogniAntonio
HayashiTamio
Soggetto topico Ferrocene
Organoiron compounds
ISBN 1-281-75871-X
9786611758714
3-527-61559-8
3-527-61558-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Ferrocenes; Preface; Contents; List of Contributors; List of Abbreviations; Part 1. Homogeneous Catalysis; 1 1,1'-Bis (dipheny1phosphino)ferrocene - Coordination Chemistry, Organic Syntheses, and Catalysis; 1.1 Introduction; 1.2 Preparation and Complexation; 1.3 Structural Properties; 1.3.1 Modes of Coordination; 1.3.2 Geometrical Distortions; 1.4 Spectroscopic Characteristics; 1.4.1 Techniques; 1.4.1.1 31P NMR Spectroscopy; 1.4.1.2 1H NMR Spectroscopy; 1.4.1.3 Mössbauer Spectroscopy; 1.4.2 NMR Fluxionality; 1.5 Catalysis; 1.5.1 Cross Coupling
1.5.1.1 Organic Electrophile and Organometallic Coupling1.5.1.2 Arylation and Vinylation of Alkenes; 1.5.1.3 Carbonylation and Carbonylative Coupling; 1.5.1.4 Nucleophilic Substitution; 1.5.1.5 Polycondensation and Polymerization; 1.5.2 Olefin Functionalization; 1.5.2.1 Hydroformylation; 1.5.2.2 Hydrogenation and Reduction; 1.5.2.3 Hydroboration and Hydrosilylation; 1.5.2.4 Isomerization; 1.6 Cluster Complexes; 1.7 Electrochemistry; 1.8 Biomedical Applications; 1.9 Summary; References; 2 Asymmetric Catalysis with Chiral Ferrocenylphosphine Ligands; 2.1 Introduction
2.2 Preparation of Chiral Ferrocenylphosphines2.3 Structure of Chiral Ferrocenylphosphines and their Transition-Metal Complexes; 2.4 Catalytic Asymmetric Reactions with Chiral Ferrocenylphosphine Ligands; 2.4.1 Cross-Coupling of Organometallics with Halides; 2.4.2 Allylic Substitution Reactions via π-Ally1 Complexes; 2.4.3 Hydrogenation of Olefins and Ketones; 2.4.4 Hydrosilylation of Olefins and Ketones; 2.4.5 Aldol Reaction of α-Isocyanocarboxylates; 2.4.6 Others; References; 3 Enantioselective Addition of Dialkylzinc to Aldehydes Catalyzed by Chiral Ferrocenyl Aminoalcohols
3.1 Introduction3.2 Chiral Ferrocenylzincs Bearing an Aminoethanol Auxiliary [12]; 3.2.1 Synthesis of the Catalysts; 3.2.2 Addition of Diethylzinc to Benzaldehyde; 3.3 N- (1-Ferrocenylalky1)-N-alk ylnorephedrines [13]; 3.3.1 Synthesis of the Catalysts; 3.3.2 Addition of Diethylzinc to Aldehydes; 3.4 Chiral Polymers Bearing N-Ferrocenylmethylephedrine [14]; 3.4.1 Synthesis of the Catalysts; 3.4.2 Addition of Diethylzinc to Benzaldehyde; 3.5 Chiral 1,2-Disubstituted Ferrocenyl Aminoalcohols [15]; 3.5.1 Synthesis of the Catalysts; 3.5.2 Addition of Dialkylzinc to Aldehydes
3.5.3 Addition of Dialkylzincs to o-Phthalaldehyde: A Facile Synthesis of Optically Active 3-Alkylphthalides [16]3.5.4 Enantio- and Diastereoselective Addition of Diethylzinc to Racemic α-Thio- and α-Selenoaldehydes [17]; 3.6 Summary; References; Part 2. Organic Synthesis - Selected Aspects; 4 Chiral Ferrocene Derivatives. An Introduction; 4.1 Central and Planar Chirality in Metallocenes; 4.2 a-Ferrocenylalkyl Carbocations; 4.2.1 Structure and Stability; 4.2.2 Stereochemistry; 4.3 Central Chiral Ferrocene Derivatives; 4.3.1 Syntheses; 4.3.1.1 By Resolution; 4.3.1.2 By Asymmetric Synthesis
4.3.1.3 From the Chiral Pool
Record Nr. UNISA-996202136003316
Weinheim ; ; New York, : VCH Publishers, c1995
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