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Catalytic methods in asymmetric synthesis [[electronic resource] ] : advanced materials, techniques, and applications / / edited by Michelangelo Gruttadauria, Francesco Giacalone
| Catalytic methods in asymmetric synthesis [[electronic resource] ] : advanced materials, techniques, and applications / / edited by Michelangelo Gruttadauria, Francesco Giacalone |
| Autore | Gruttadauria Michelangelo |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, 2011 |
| Descrizione fisica | 1 online resource (722 p.) |
| Disciplina | 541/.395 |
| Altri autori (Persone) |
GruttadauriaMichelangelo
GiacaloneFrancesco |
| Soggetto topico |
Asymmetric synthesis
Catalysis |
| ISBN |
1-283-20394-4
9786613203946 1-118-08798-4 1-118-08799-2 1-118-08797-6 |
| Classificazione | SCI013040 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Machine generated contents note: Part I. New materials and technologies: supported catalysts, supports, self-supported catalysts, chiral ionic liquid, supercritical fluids, flow reactors and microwaves.1.Recyclable stereoselective catalysts (Carlos M. Monteiro, Alexandre F. Trindale, Pedro M. P. Gois and Carlos A. M. Afonso).2. Recyclable organocatalysts in asymmetric reactions (Michelangelo Gruttadauria, Francesco Giacalone and Renato Noto).3. Synthesis and characterization of supported chiral catalysts (Carmela Aprile, Hermenegildo Garcia and Paolo Pescarmona).4. Synthesis of chiral catalysts supported on organic polymers (Tor Erik Kristensen and Tore Hansen).5. Self-supported chiral catalysts (Hongchao Guo and Kuiling Ding).6. Catalysis with chirally modified metal surfaces: scope and mechanisms (Angelo Vargas, Cecilia Mondelli and Alfons Baiker).7. Chiral ionic liquids for asymmetric reactions (Annie-Claude Gaumont, Yves Ge;nisson, Fre;de;ric Guillen and Jean-Christophe Plaquevent).8. Asymmetric reactions in flow reactors (Munawwer Racheed, Simon C. Elmore and Thomas Wirth).9. Asymmetric catalytic synthesis in supercritical fluids (Tomoko Matsuda).10. Microwave-assisted transition metal-catalyzed asymmetric synthesis (Luke R. Odell and Mats Larhed).Part II. Recent advances in organocatalytic, enzymatic and metal-based mediated asymmetric synthesis.11. Recent advances on stereoselective organocatalytic reactions. Organocatalytic synthesis of natural products and drugs (Monika Ray and Vinod K. Singh). 12. Recent advances in biocatalysis applied to organic synthesis (Gonzalo de Gonzalo, Iván Lavandera and Vicente Gotor).13. Peptides for asymmetric catalysis (Matthias Freund and Svetlana Tsogoeva).14. Siliciate-mediated steroselective reactions catalyzed by chiral Lewis bases (Maurizio Benaglia, Stefania Guizzetti and Sergio Rossi).15. Recent advances in the metal-ctalyzed steroselective synthesis of biologically active molecules (Catalina Ferrer, Xavier Verdaguer and Antoni Riera).16. Stereoselective nitrogen heterocycles synthesis mediated by chiral metal catalysts (Sherry R. Chemler). |
| Record Nr. | UNINA-9910139642403321 |
Gruttadauria Michelangelo
|
||
| Hoboken, N.J., : Wiley, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Catalytic methods in asymmetric synthesis [[electronic resource] ] : advanced materials, techniques, and applications / / edited by Michelangelo Gruttadauria, Francesco Giacalone
| Catalytic methods in asymmetric synthesis [[electronic resource] ] : advanced materials, techniques, and applications / / edited by Michelangelo Gruttadauria, Francesco Giacalone |
| Autore | Gruttadauria Michelangelo |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, 2011 |
| Descrizione fisica | 1 online resource (722 p.) |
| Disciplina | 541/.395 |
| Altri autori (Persone) |
GruttadauriaMichelangelo
GiacaloneFrancesco |
| Soggetto topico |
Asymmetric synthesis
Catalysis |
| ISBN |
1-283-20394-4
9786613203946 1-118-08798-4 1-118-08799-2 1-118-08797-6 |
| Classificazione | SCI013040 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Machine generated contents note: Part I. New materials and technologies: supported catalysts, supports, self-supported catalysts, chiral ionic liquid, supercritical fluids, flow reactors and microwaves.1.Recyclable stereoselective catalysts (Carlos M. Monteiro, Alexandre F. Trindale, Pedro M. P. Gois and Carlos A. M. Afonso).2. Recyclable organocatalysts in asymmetric reactions (Michelangelo Gruttadauria, Francesco Giacalone and Renato Noto).3. Synthesis and characterization of supported chiral catalysts (Carmela Aprile, Hermenegildo Garcia and Paolo Pescarmona).4. Synthesis of chiral catalysts supported on organic polymers (Tor Erik Kristensen and Tore Hansen).5. Self-supported chiral catalysts (Hongchao Guo and Kuiling Ding).6. Catalysis with chirally modified metal surfaces: scope and mechanisms (Angelo Vargas, Cecilia Mondelli and Alfons Baiker).7. Chiral ionic liquids for asymmetric reactions (Annie-Claude Gaumont, Yves Ge;nisson, Fre;de;ric Guillen and Jean-Christophe Plaquevent).8. Asymmetric reactions in flow reactors (Munawwer Racheed, Simon C. Elmore and Thomas Wirth).9. Asymmetric catalytic synthesis in supercritical fluids (Tomoko Matsuda).10. Microwave-assisted transition metal-catalyzed asymmetric synthesis (Luke R. Odell and Mats Larhed).Part II. Recent advances in organocatalytic, enzymatic and metal-based mediated asymmetric synthesis.11. Recent advances on stereoselective organocatalytic reactions. Organocatalytic synthesis of natural products and drugs (Monika Ray and Vinod K. Singh). 12. Recent advances in biocatalysis applied to organic synthesis (Gonzalo de Gonzalo, Iván Lavandera and Vicente Gotor).13. Peptides for asymmetric catalysis (Matthias Freund and Svetlana Tsogoeva).14. Siliciate-mediated steroselective reactions catalyzed by chiral Lewis bases (Maurizio Benaglia, Stefania Guizzetti and Sergio Rossi).15. Recent advances in the metal-ctalyzed steroselective synthesis of biologically active molecules (Catalina Ferrer, Xavier Verdaguer and Antoni Riera).16. Stereoselective nitrogen heterocycles synthesis mediated by chiral metal catalysts (Sherry R. Chemler). |
| Record Nr. | UNINA-9910822003103321 |
|
Gruttadauria Michelangelo
|
||
| Hoboken, N.J., : Wiley, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Fullerene polymers [[electronic resource] ] : synthesis, properties and applications / / edited by Nazario Martin, Francesco Giacalone
| Fullerene polymers [[electronic resource] ] : synthesis, properties and applications / / edited by Nazario Martin, Francesco Giacalone |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2009 |
| Descrizione fisica | 1 online resource (331 p.) |
| Disciplina |
546.681
620.193 |
| Altri autori (Persone) |
MartinNazario
GiacaloneFrancesco |
| Soggetto topico |
Fullerene polymers
Fullerene polymers - Synthesis Fullerene polymers - Industrial applications |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-27853-3
9786612278532 3-527-62874-6 3-527-62875-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Fullerene Polymers; Foreword; Contents; Preface; Contributors; 1: Fullerene-Containing Polymers: An Overview; 1.1 Polyfullerenes: A Brief History; 1.2 Classification of Polyfullerenes; 1.2.1 All-C60 Polymers; 1.2.2 Organometallic Polymers; 1.2.3 Crosslinked Polymers; 1.2.4 End-Capped Polymers; 1.2.5 C60-Dendrimers; 1.2.6 Star-Shaped Polymers; 1.2.7 Main-Chain Polymers; 1.2.8 Side-Chain Polymers; 1.2.8.1 Double-Cable Polymers; 1.2.9 Supramolecular Polymers; 1.3 Outlook and Perspective; References; 2: Main-Chain and Side-Chain C60-Polymers; 2.1 Introduction; 2.2 Main-Chain Polymers
2.3 Side-Chain Polymers2.3.1 Polystyrene-C60 Polymers; 2.3.2 Polyacrylate-and Methacrylate-C60 Polymers and Copolymers; 2.3.3 Polycarbonate-C60 Polymers; 2.3.4 Aminofishing Side-Chain Polymers; 2.3.5 Polyvinylcarbazoles; 2.3.6 Polyphosphazenes and Polysiloxanes; 2.3.7 Side-Chain C60-Polysaccarides; 2.3.8 Polyether-C60 Polymers; 2.3.9 Side-Chain Polymers Prepared by Organometallic Catalysis; 2.4 Conclusions and Further Perspectives; References; 3: Acrylate and Methacrylate C60-End-Capped Polymers; 3.1 Introduction; 3.2 Synthesis of C60-End-Capped Polymers 3.2.1 General Synthetic Approaches for C60-Containing Polymers3.2.2 Well-Defined C60 End-Capped Polymers by Controlled Radical Polymerization; 3.3 Aggregation of C60-End-Capped Polymers in Solution; 3.3.1 Self-Assembly of C60-End-Capped Polymers in Organic Solvents; 3.3.2 Aggregation of C60-End-Capped Polymers in Aqueous Solution; 3.3.2.1 pH-Responsive C60-Containing Polymers; 3.3.2.2 Temperature-Responsive C60-Containing Polymers; 3.3.2.3 C60-Containing Polyampholytes; 3.3.2.4 Supramolecular Fractal Patterning; 3.3.2.5 Surfactant Induced Nano-Structures; 3.4 Summary; References 4: Semi-Interpenetrating Polymer Networks Involving C60-Polymers4.1 Introduction; 4.2 Synthesis and Properties of Double-C60-End-Capped Polymers; 4.3 Mechanical Properties of Pseudo-SIPNs; 4.3.1 FPEOF/PMMA Pseudo-SIPNs; 4.3.2 FPEOF/Poly(L-Lactic Acid)Pseudo-SIPNs; 4.3.3 FPBMAF/PVC Pseudo-SIPNs; 4.4 Optical Transmission Characteristics of Pseudo-SIPNs; 4.5 Conclusions; References; 5: Star-Shaped Polymers with a Fullerene Core; 5.1 Introduction; 5.2 Grafting of Linear Polymer Chains onto C60; 5.2.1 Grafting via Radicals; 5.2.1.1 Radical Copolymerization of Fullerenes with Vinyl Monomers 5.2.1.2 Addition of Macro-radicals Obtained by"Controlled" Radical Polymerization5.2.1.3 Addition of Macro-radicals Obtained by Cleavage of Macro-initiators; 5.2.2 Grafting via Nucleophilic Addition; 5.2.2.1 Grafting of Neutral Nucleophiles; 5.2.2.2 Grafting of Charged Nucleophiles; 5.2.3 Other Grafting Reactions; 5.3 Polymerization of a Monomer Using Charged or Functionalized Fullerenes as Initiators; 5.3.1 Controlled Radical Polymerization Using a C60(X)n as Initiator 5.3.2 Anionic Polymerization Initiated by Fullerides C60x-(M+)x or "Living" Polymer Stars with a Fullerene Core (Polymer)x C60x-(M+)x ( x 6 |
| Record Nr. | UNINA-9910139932903321 |
| Weinheim, : Wiley-VCH, 2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Fullerene polymers [[electronic resource] ] : synthesis, properties and applications / / edited by Nazario Martin, Francesco Giacalone
| Fullerene polymers [[electronic resource] ] : synthesis, properties and applications / / edited by Nazario Martin, Francesco Giacalone |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2009 |
| Descrizione fisica | 1 online resource (331 p.) |
| Disciplina |
546.681
620.193 |
| Altri autori (Persone) |
MartinNazario
GiacaloneFrancesco |
| Soggetto topico |
Fullerene polymers
Fullerene polymers - Synthesis Fullerene polymers - Industrial applications |
| ISBN |
1-282-27853-3
9786612278532 3-527-62874-6 3-527-62875-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Fullerene Polymers; Foreword; Contents; Preface; Contributors; 1: Fullerene-Containing Polymers: An Overview; 1.1 Polyfullerenes: A Brief History; 1.2 Classification of Polyfullerenes; 1.2.1 All-C60 Polymers; 1.2.2 Organometallic Polymers; 1.2.3 Crosslinked Polymers; 1.2.4 End-Capped Polymers; 1.2.5 C60-Dendrimers; 1.2.6 Star-Shaped Polymers; 1.2.7 Main-Chain Polymers; 1.2.8 Side-Chain Polymers; 1.2.8.1 Double-Cable Polymers; 1.2.9 Supramolecular Polymers; 1.3 Outlook and Perspective; References; 2: Main-Chain and Side-Chain C60-Polymers; 2.1 Introduction; 2.2 Main-Chain Polymers
2.3 Side-Chain Polymers2.3.1 Polystyrene-C60 Polymers; 2.3.2 Polyacrylate-and Methacrylate-C60 Polymers and Copolymers; 2.3.3 Polycarbonate-C60 Polymers; 2.3.4 Aminofishing Side-Chain Polymers; 2.3.5 Polyvinylcarbazoles; 2.3.6 Polyphosphazenes and Polysiloxanes; 2.3.7 Side-Chain C60-Polysaccarides; 2.3.8 Polyether-C60 Polymers; 2.3.9 Side-Chain Polymers Prepared by Organometallic Catalysis; 2.4 Conclusions and Further Perspectives; References; 3: Acrylate and Methacrylate C60-End-Capped Polymers; 3.1 Introduction; 3.2 Synthesis of C60-End-Capped Polymers 3.2.1 General Synthetic Approaches for C60-Containing Polymers3.2.2 Well-Defined C60 End-Capped Polymers by Controlled Radical Polymerization; 3.3 Aggregation of C60-End-Capped Polymers in Solution; 3.3.1 Self-Assembly of C60-End-Capped Polymers in Organic Solvents; 3.3.2 Aggregation of C60-End-Capped Polymers in Aqueous Solution; 3.3.2.1 pH-Responsive C60-Containing Polymers; 3.3.2.2 Temperature-Responsive C60-Containing Polymers; 3.3.2.3 C60-Containing Polyampholytes; 3.3.2.4 Supramolecular Fractal Patterning; 3.3.2.5 Surfactant Induced Nano-Structures; 3.4 Summary; References 4: Semi-Interpenetrating Polymer Networks Involving C60-Polymers4.1 Introduction; 4.2 Synthesis and Properties of Double-C60-End-Capped Polymers; 4.3 Mechanical Properties of Pseudo-SIPNs; 4.3.1 FPEOF/PMMA Pseudo-SIPNs; 4.3.2 FPEOF/Poly(L-Lactic Acid)Pseudo-SIPNs; 4.3.3 FPBMAF/PVC Pseudo-SIPNs; 4.4 Optical Transmission Characteristics of Pseudo-SIPNs; 4.5 Conclusions; References; 5: Star-Shaped Polymers with a Fullerene Core; 5.1 Introduction; 5.2 Grafting of Linear Polymer Chains onto C60; 5.2.1 Grafting via Radicals; 5.2.1.1 Radical Copolymerization of Fullerenes with Vinyl Monomers 5.2.1.2 Addition of Macro-radicals Obtained by"Controlled" Radical Polymerization5.2.1.3 Addition of Macro-radicals Obtained by Cleavage of Macro-initiators; 5.2.2 Grafting via Nucleophilic Addition; 5.2.2.1 Grafting of Neutral Nucleophiles; 5.2.2.2 Grafting of Charged Nucleophiles; 5.2.3 Other Grafting Reactions; 5.3 Polymerization of a Monomer Using Charged or Functionalized Fullerenes as Initiators; 5.3.1 Controlled Radical Polymerization Using a C60(X)n as Initiator 5.3.2 Anionic Polymerization Initiated by Fullerides C60x-(M+)x or "Living" Polymer Stars with a Fullerene Core (Polymer)x C60x-(M+)x ( x 6 |
| Record Nr. | UNINA-9910830438103321 |
| Weinheim, : Wiley-VCH, 2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Fullerene polymers : synthesis, properties and applications / / edited by Nazario Martin, Francesco Giacalone
| Fullerene polymers : synthesis, properties and applications / / edited by Nazario Martin, Francesco Giacalone |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2009 |
| Descrizione fisica | 1 online resource (331 p.) |
| Disciplina |
546.681
620.193 |
| Altri autori (Persone) |
MartinNazario
GiacaloneFrancesco |
| Soggetto topico |
Fullerene polymers
Fullerene polymers - Synthesis Fullerene polymers - Industrial applications |
| ISBN |
1-282-27853-3
9786612278532 3-527-62874-6 3-527-62875-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Fullerene Polymers; Foreword; Contents; Preface; Contributors; 1: Fullerene-Containing Polymers: An Overview; 1.1 Polyfullerenes: A Brief History; 1.2 Classification of Polyfullerenes; 1.2.1 All-C60 Polymers; 1.2.2 Organometallic Polymers; 1.2.3 Crosslinked Polymers; 1.2.4 End-Capped Polymers; 1.2.5 C60-Dendrimers; 1.2.6 Star-Shaped Polymers; 1.2.7 Main-Chain Polymers; 1.2.8 Side-Chain Polymers; 1.2.8.1 Double-Cable Polymers; 1.2.9 Supramolecular Polymers; 1.3 Outlook and Perspective; References; 2: Main-Chain and Side-Chain C60-Polymers; 2.1 Introduction; 2.2 Main-Chain Polymers
2.3 Side-Chain Polymers2.3.1 Polystyrene-C60 Polymers; 2.3.2 Polyacrylate-and Methacrylate-C60 Polymers and Copolymers; 2.3.3 Polycarbonate-C60 Polymers; 2.3.4 Aminofishing Side-Chain Polymers; 2.3.5 Polyvinylcarbazoles; 2.3.6 Polyphosphazenes and Polysiloxanes; 2.3.7 Side-Chain C60-Polysaccarides; 2.3.8 Polyether-C60 Polymers; 2.3.9 Side-Chain Polymers Prepared by Organometallic Catalysis; 2.4 Conclusions and Further Perspectives; References; 3: Acrylate and Methacrylate C60-End-Capped Polymers; 3.1 Introduction; 3.2 Synthesis of C60-End-Capped Polymers 3.2.1 General Synthetic Approaches for C60-Containing Polymers3.2.2 Well-Defined C60 End-Capped Polymers by Controlled Radical Polymerization; 3.3 Aggregation of C60-End-Capped Polymers in Solution; 3.3.1 Self-Assembly of C60-End-Capped Polymers in Organic Solvents; 3.3.2 Aggregation of C60-End-Capped Polymers in Aqueous Solution; 3.3.2.1 pH-Responsive C60-Containing Polymers; 3.3.2.2 Temperature-Responsive C60-Containing Polymers; 3.3.2.3 C60-Containing Polyampholytes; 3.3.2.4 Supramolecular Fractal Patterning; 3.3.2.5 Surfactant Induced Nano-Structures; 3.4 Summary; References 4: Semi-Interpenetrating Polymer Networks Involving C60-Polymers4.1 Introduction; 4.2 Synthesis and Properties of Double-C60-End-Capped Polymers; 4.3 Mechanical Properties of Pseudo-SIPNs; 4.3.1 FPEOF/PMMA Pseudo-SIPNs; 4.3.2 FPEOF/Poly(L-Lactic Acid)Pseudo-SIPNs; 4.3.3 FPBMAF/PVC Pseudo-SIPNs; 4.4 Optical Transmission Characteristics of Pseudo-SIPNs; 4.5 Conclusions; References; 5: Star-Shaped Polymers with a Fullerene Core; 5.1 Introduction; 5.2 Grafting of Linear Polymer Chains onto C60; 5.2.1 Grafting via Radicals; 5.2.1.1 Radical Copolymerization of Fullerenes with Vinyl Monomers 5.2.1.2 Addition of Macro-radicals Obtained by"Controlled" Radical Polymerization5.2.1.3 Addition of Macro-radicals Obtained by Cleavage of Macro-initiators; 5.2.2 Grafting via Nucleophilic Addition; 5.2.2.1 Grafting of Neutral Nucleophiles; 5.2.2.2 Grafting of Charged Nucleophiles; 5.2.3 Other Grafting Reactions; 5.3 Polymerization of a Monomer Using Charged or Functionalized Fullerenes as Initiators; 5.3.1 Controlled Radical Polymerization Using a C60(X)n as Initiator 5.3.2 Anionic Polymerization Initiated by Fullerides C60x-(M+)x or "Living" Polymer Stars with a Fullerene Core (Polymer)x C60x-(M+)x ( x 6 |
| Record Nr. | UNINA-9910840860803321 |
| Weinheim, : Wiley-VCH, 2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||