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Carbon dioxide thermodynamic properties handbook [[electronic resource] ] : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Carbon dioxide thermodynamic properties handbook [[electronic resource] ] : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Autore Anwar Sara
Pubbl/distr/stampa Hoboken, New Jersey, : John Wiley & Sons
Descrizione fisica 1 online resource (590 p.)
Disciplina 546.6812
546/.6812
Altri autori (Persone) CarrollJohn J. <1958->
Soggetto topico Carbon dioxide - Thermal properties
Carbon compounds
Soggetto genere / forma Electronic books.
ISBN 1-118-09950-8
1-283-37447-1
9786613374479
1-118-06568-9
1-61344-188-6
1-118-06569-7
Classificazione TEC031030
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon Dioxide Thermodynamic Properties Handbook Covering Temperatures from -20° to 250°C and Pressures up to 1000 bar; Contents; Acknowledgement; Preface; Introduction; 1 Density (kg/m3) of Saturated Carbon Dioxide; 2 Enthalpy (J/mol) of Saturated Carbon Dioxide; 3 Entropy (J/mol ·Κ) of Saturated Carbon Dioxide; 4 Heat Capacity, Cp, (J/mol · K) of Saturated Carbon Dioxide; 5 Density (kg/m3) of Carbon Dioxide as a Function of Temperature and Pressure; 6 Enthalpy (J/mol) of Carbon Dioxide as a Function of Temperature and Pressure
7 Entropy (J/mol ·Κ) of Carbon Dioxide as a Function of Temperature and Pressure8 Heat Capacity, Cp, (J/mol · K) of Carbon Dioxide as a Function of Temperature and Pressure
Record Nr. UNINA-9910133451103321
Anwar Sara  
Hoboken, New Jersey, : John Wiley & Sons
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Carbon dioxide thermodynamic properties handbook [[electronic resource] ] : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Carbon dioxide thermodynamic properties handbook [[electronic resource] ] : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Autore Anwar Sara
Pubbl/distr/stampa Hoboken, New Jersey, : John Wiley & Sons
Descrizione fisica 1 online resource (590 p.)
Disciplina 546.6812
546/.6812
Altri autori (Persone) CarrollJohn J. <1958->
Soggetto topico Carbon dioxide - Thermal properties
Carbon compounds
ISBN 1-118-09950-8
1-283-37447-1
9786613374479
1-118-06568-9
1-61344-188-6
1-118-06569-7
Classificazione TEC031030
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon Dioxide Thermodynamic Properties Handbook Covering Temperatures from -20° to 250°C and Pressures up to 1000 bar; Contents; Acknowledgement; Preface; Introduction; 1 Density (kg/m3) of Saturated Carbon Dioxide; 2 Enthalpy (J/mol) of Saturated Carbon Dioxide; 3 Entropy (J/mol ·Κ) of Saturated Carbon Dioxide; 4 Heat Capacity, Cp, (J/mol · K) of Saturated Carbon Dioxide; 5 Density (kg/m3) of Carbon Dioxide as a Function of Temperature and Pressure; 6 Enthalpy (J/mol) of Carbon Dioxide as a Function of Temperature and Pressure
7 Entropy (J/mol ·Κ) of Carbon Dioxide as a Function of Temperature and Pressure8 Heat Capacity, Cp, (J/mol · K) of Carbon Dioxide as a Function of Temperature and Pressure
Record Nr. UNINA-9910830047103321
Anwar Sara  
Hoboken, New Jersey, : John Wiley & Sons
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon dioxide thermodynamic properties handbook : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Carbon dioxide thermodynamic properties handbook : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Autore Anwar Sara
Pubbl/distr/stampa Hoboken, New Jersey, : John Wiley & Sons
Descrizione fisica 1 online resource (590 p.)
Disciplina 546.6812
546/.6812
Altri autori (Persone) CarrollJohn J. <1958->
Soggetto topico Carbon dioxide - Thermal properties
Carbon compounds
ISBN 1-118-09950-8
1-283-37447-1
9786613374479
1-118-06568-9
1-61344-188-6
1-118-06569-7
Classificazione TEC031030
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon Dioxide Thermodynamic Properties Handbook Covering Temperatures from -20° to 250°C and Pressures up to 1000 bar; Contents; Acknowledgement; Preface; Introduction; 1 Density (kg/m3) of Saturated Carbon Dioxide; 2 Enthalpy (J/mol) of Saturated Carbon Dioxide; 3 Entropy (J/mol ·Κ) of Saturated Carbon Dioxide; 4 Heat Capacity, Cp, (J/mol · K) of Saturated Carbon Dioxide; 5 Density (kg/m3) of Carbon Dioxide as a Function of Temperature and Pressure; 6 Enthalpy (J/mol) of Carbon Dioxide as a Function of Temperature and Pressure
7 Entropy (J/mol ·Κ) of Carbon Dioxide as a Function of Temperature and Pressure8 Heat Capacity, Cp, (J/mol · K) of Carbon Dioxide as a Function of Temperature and Pressure
Record Nr. UNINA-9910876791303321
Anwar Sara  
Hoboken, New Jersey, : John Wiley & Sons
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Carbon-based solids and materials [[electronic resource] /] / Pierre Delhaes
Carbon-based solids and materials [[electronic resource] /] / Pierre Delhaes
Autore Delhaes Pierre
Pubbl/distr/stampa London, : ISTE
Descrizione fisica 1 online resource (658 p.)
Disciplina 620.1/93
620.193
Collana ISTE
Soggetto topico Carbon composites
Carbon compounds
Soggetto genere / forma Electronic books.
ISBN 1-118-55761-1
1-118-60088-6
1-118-60089-4
1-299-18749-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Carbon phases, precursors and parent compounds -- pt. 2. Physical properties of solid carbons -- pt. 3. Carbon materials and uses.
Record Nr. UNINA-9910138852603321
Delhaes Pierre  
London, : ISTE
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Carbon-based solids and materials [[electronic resource] /] / Pierre Delhaes
Carbon-based solids and materials [[electronic resource] /] / Pierre Delhaes
Autore Delhaes Pierre
Pubbl/distr/stampa London, : ISTE
Descrizione fisica 1 online resource (658 p.)
Disciplina 620.1/93
620.193
Collana ISTE
Soggetto topico Carbon composites
Carbon compounds
ISBN 1-118-55761-1
1-118-60088-6
1-118-60089-4
1-299-18749-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Carbon phases, precursors and parent compounds -- pt. 2. Physical properties of solid carbons -- pt. 3. Carbon materials and uses.
Record Nr. UNINA-9910830086603321
Delhaes Pierre  
London, : ISTE
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Carbon-based solids and materials / / Pierre Delhaes
Carbon-based solids and materials / / Pierre Delhaes
Autore Delhaes Pierre
Pubbl/distr/stampa London, : ISTE
Descrizione fisica 1 online resource (658 p.)
Disciplina 620.1/93
Collana ISTE
Soggetto topico Carbon composites
Carbon compounds
ISBN 1-118-55761-1
1-118-60088-6
1-118-60089-4
1-299-18749-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Carbon phases, precursors and parent compounds -- pt. 2. Physical properties of solid carbons -- pt. 3. Carbon materials and uses.
Record Nr. UNINA-9910877273403321
Delhaes Pierre  
London, : ISTE
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Carbon-rich compounds [[electronic resource] ] : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Carbon-rich compounds [[electronic resource] ] : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Pubbl/distr/stampa Weinheim, : Wiley-VCH
Descrizione fisica 1 online resource (665 p.)
Disciplina 547
Altri autori (Persone) HaleyMichael
TykwinskiR. R (Rik R.)
Soggetto topico Carbon compounds
Chemistry, Organic
Soggetto genere / forma Electronic books.
ISBN 1-280-85431-6
9786610854318
3-527-60799-4
3-527-60724-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon-Rich Compounds; Foreword; Contents; Preface; List of Contributors; 1 Pioneers of Carbon-rich Compounds; 1.1 Introduction; 1.2 19th Century Achievements; 1.3 1900-1928: Dawn of the Twentieth Century; 1.4 1929-1949: Rise of the Polycyclic Aromatic Hydrocarbon; 1.5 1950-1969; 1.5.1 The Annulenes, Dehydrobenzoannulenes, and Phenylacetylene Scaffolding; 1.5.2 Fused Polycyclic and peri-Condensed Benzenoid Systems; 1.5.3 The Helicenes, Radialenes, Fulvalenes, and Circulenes; 1.6 1970-Present: The Way Ahead; References; 2 Electronic Conduction in Photoactive Metallo-wires; 2.1 Introduction
2.2 Attenuation along Molecular Bridges2.3 Information Transfer; 2.3.1 Intramolecular Triplet Energy Transfer; 2.3.2 Short Covalent Bridges; 2.3.3 Supramolecular Systems; 2.3.4 Prolonging the Excited State Lifetime; 2.3.5 Long-range Triplet Energy Transfer; 2.4 Molecular-scale Switches; 2.5 Perspectives; 2.6 Experimental: Selected Procedures; 2.6.1 General Procedure for the Preparation of the Mononuclear [RuL(n)]; 2.6.2 General Procedure for the Preparation of the Hetero-Dinuclear Complexes 81(1) and 81(5); 2.6.3 Synthesis at the Complex; Acknowledgements; Abbreviations; References
3 All-benzenoid Polycyclic Aromatic Hydrocarbons: Synthesis, Self-assembly and Applications in Organic Electronics3.1 A Brief Introduction to Polycyclic Aromatic Hydrocarbons; 3.2 All-benzenoid PAHs - Synthesis, Structural Characterizations and Electronic Properties; 3.2.1 Hexa-peri-hexabenzocoronene - An Old Story with New Discoveries; 3.2.2 All-benzenoid Graphitic PAHs Larger than HBCs; 3.2.3 PAHs with Varying Peripheries; 3.2.4 ''Superbenzene'' Chemistry and Others; 3.3 Self-assembly and Application of Columnar Liquid Crystals based on PBAHs
3.3.1 Columnar Superstructures in the Bulk State3.3.2 Alignment on Substrates and Device Applications of Columnar Liquid Crystals; 3.3.3 Controlled Self-assembly in Solution; 3.3.4 Two-dimensional Crystals at the Solid/Liquid Interface; 3.4 Conclusion; 3.5 Experimental: Selected Procedures; 3.5.1 Synthesis of hexa-peri-hexabenzocoronene 10 by Cu(II)-mediated oxidative cyclodehydrogenation - a general procedure to prepare unsubstituted graphitic molecules [35]
3.5.2 Synthesis of hexakis(4-dodecylphenyl)-peri-hexabenzocoronene (HBC-PhC12) - a general synthetic method towards six-fold alkyl- and alkylphenyl-substituted HBCs [38]3.5.3 Functionalization of insoluble HBC building blocks 30-32 by Sonogashira coupling reactions [48]. Synthesis of hexakis(1-dodecynylphenyl)-peri-hexabenzocoronene (34a) as a representative example; 3.5.4 Synthesis of C96-C12 precursor 1,3,5-tris[3 ́,4 ́-di(4 ́ ́-dodecylphenyl)-2 ́,5 ́-diphenylphenyl]benzene (44a) by Diels-Alder cycloaddition reaction - a representative procedure for the synthesis of branched oligophenylenes [50]
3.5.5 Hydrogenation of hexakis-dodecyl-peri-hexabenzocoronenes 74 [66]
Record Nr. UNINA-9910144321703321
Weinheim, : Wiley-VCH
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon-rich compounds [[electronic resource] ] : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Carbon-rich compounds [[electronic resource] ] : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Pubbl/distr/stampa Weinheim, : Wiley-VCH
Descrizione fisica 1 online resource (665 p.)
Disciplina 547
Altri autori (Persone) HaleyMichael
TykwinskiR. R (Rik R.)
Soggetto topico Carbon compounds
Chemistry, Organic
ISBN 1-280-85431-6
9786610854318
3-527-60799-4
3-527-60724-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon-Rich Compounds; Foreword; Contents; Preface; List of Contributors; 1 Pioneers of Carbon-rich Compounds; 1.1 Introduction; 1.2 19th Century Achievements; 1.3 1900-1928: Dawn of the Twentieth Century; 1.4 1929-1949: Rise of the Polycyclic Aromatic Hydrocarbon; 1.5 1950-1969; 1.5.1 The Annulenes, Dehydrobenzoannulenes, and Phenylacetylene Scaffolding; 1.5.2 Fused Polycyclic and peri-Condensed Benzenoid Systems; 1.5.3 The Helicenes, Radialenes, Fulvalenes, and Circulenes; 1.6 1970-Present: The Way Ahead; References; 2 Electronic Conduction in Photoactive Metallo-wires; 2.1 Introduction
2.2 Attenuation along Molecular Bridges2.3 Information Transfer; 2.3.1 Intramolecular Triplet Energy Transfer; 2.3.2 Short Covalent Bridges; 2.3.3 Supramolecular Systems; 2.3.4 Prolonging the Excited State Lifetime; 2.3.5 Long-range Triplet Energy Transfer; 2.4 Molecular-scale Switches; 2.5 Perspectives; 2.6 Experimental: Selected Procedures; 2.6.1 General Procedure for the Preparation of the Mononuclear [RuL(n)]; 2.6.2 General Procedure for the Preparation of the Hetero-Dinuclear Complexes 81(1) and 81(5); 2.6.3 Synthesis at the Complex; Acknowledgements; Abbreviations; References
3 All-benzenoid Polycyclic Aromatic Hydrocarbons: Synthesis, Self-assembly and Applications in Organic Electronics3.1 A Brief Introduction to Polycyclic Aromatic Hydrocarbons; 3.2 All-benzenoid PAHs - Synthesis, Structural Characterizations and Electronic Properties; 3.2.1 Hexa-peri-hexabenzocoronene - An Old Story with New Discoveries; 3.2.2 All-benzenoid Graphitic PAHs Larger than HBCs; 3.2.3 PAHs with Varying Peripheries; 3.2.4 ''Superbenzene'' Chemistry and Others; 3.3 Self-assembly and Application of Columnar Liquid Crystals based on PBAHs
3.3.1 Columnar Superstructures in the Bulk State3.3.2 Alignment on Substrates and Device Applications of Columnar Liquid Crystals; 3.3.3 Controlled Self-assembly in Solution; 3.3.4 Two-dimensional Crystals at the Solid/Liquid Interface; 3.4 Conclusion; 3.5 Experimental: Selected Procedures; 3.5.1 Synthesis of hexa-peri-hexabenzocoronene 10 by Cu(II)-mediated oxidative cyclodehydrogenation - a general procedure to prepare unsubstituted graphitic molecules [35]
3.5.2 Synthesis of hexakis(4-dodecylphenyl)-peri-hexabenzocoronene (HBC-PhC12) - a general synthetic method towards six-fold alkyl- and alkylphenyl-substituted HBCs [38]3.5.3 Functionalization of insoluble HBC building blocks 30-32 by Sonogashira coupling reactions [48]. Synthesis of hexakis(1-dodecynylphenyl)-peri-hexabenzocoronene (34a) as a representative example; 3.5.4 Synthesis of C96-C12 precursor 1,3,5-tris[3 ́,4 ́-di(4 ́ ́-dodecylphenyl)-2 ́,5 ́-diphenylphenyl]benzene (44a) by Diels-Alder cycloaddition reaction - a representative procedure for the synthesis of branched oligophenylenes [50]
3.5.5 Hydrogenation of hexakis-dodecyl-peri-hexabenzocoronenes 74 [66]
Record Nr. UNINA-9910830795503321
Weinheim, : Wiley-VCH
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon-rich compounds : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Carbon-rich compounds : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Pubbl/distr/stampa Weinheim, : Wiley-VCH
Descrizione fisica 1 online resource (665 p.)
Disciplina 547
Altri autori (Persone) HaleyMichael
TykwinskiR. R (Rik R.)
Soggetto topico Carbon compounds
Chemistry, Organic
ISBN 1-280-85431-6
9786610854318
3-527-60799-4
3-527-60724-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon-Rich Compounds; Foreword; Contents; Preface; List of Contributors; 1 Pioneers of Carbon-rich Compounds; 1.1 Introduction; 1.2 19th Century Achievements; 1.3 1900-1928: Dawn of the Twentieth Century; 1.4 1929-1949: Rise of the Polycyclic Aromatic Hydrocarbon; 1.5 1950-1969; 1.5.1 The Annulenes, Dehydrobenzoannulenes, and Phenylacetylene Scaffolding; 1.5.2 Fused Polycyclic and peri-Condensed Benzenoid Systems; 1.5.3 The Helicenes, Radialenes, Fulvalenes, and Circulenes; 1.6 1970-Present: The Way Ahead; References; 2 Electronic Conduction in Photoactive Metallo-wires; 2.1 Introduction
2.2 Attenuation along Molecular Bridges2.3 Information Transfer; 2.3.1 Intramolecular Triplet Energy Transfer; 2.3.2 Short Covalent Bridges; 2.3.3 Supramolecular Systems; 2.3.4 Prolonging the Excited State Lifetime; 2.3.5 Long-range Triplet Energy Transfer; 2.4 Molecular-scale Switches; 2.5 Perspectives; 2.6 Experimental: Selected Procedures; 2.6.1 General Procedure for the Preparation of the Mononuclear [RuL(n)]; 2.6.2 General Procedure for the Preparation of the Hetero-Dinuclear Complexes 81(1) and 81(5); 2.6.3 Synthesis at the Complex; Acknowledgements; Abbreviations; References
3 All-benzenoid Polycyclic Aromatic Hydrocarbons: Synthesis, Self-assembly and Applications in Organic Electronics3.1 A Brief Introduction to Polycyclic Aromatic Hydrocarbons; 3.2 All-benzenoid PAHs - Synthesis, Structural Characterizations and Electronic Properties; 3.2.1 Hexa-peri-hexabenzocoronene - An Old Story with New Discoveries; 3.2.2 All-benzenoid Graphitic PAHs Larger than HBCs; 3.2.3 PAHs with Varying Peripheries; 3.2.4 ''Superbenzene'' Chemistry and Others; 3.3 Self-assembly and Application of Columnar Liquid Crystals based on PBAHs
3.3.1 Columnar Superstructures in the Bulk State3.3.2 Alignment on Substrates and Device Applications of Columnar Liquid Crystals; 3.3.3 Controlled Self-assembly in Solution; 3.3.4 Two-dimensional Crystals at the Solid/Liquid Interface; 3.4 Conclusion; 3.5 Experimental: Selected Procedures; 3.5.1 Synthesis of hexa-peri-hexabenzocoronene 10 by Cu(II)-mediated oxidative cyclodehydrogenation - a general procedure to prepare unsubstituted graphitic molecules [35]
3.5.2 Synthesis of hexakis(4-dodecylphenyl)-peri-hexabenzocoronene (HBC-PhC12) - a general synthetic method towards six-fold alkyl- and alkylphenyl-substituted HBCs [38]3.5.3 Functionalization of insoluble HBC building blocks 30-32 by Sonogashira coupling reactions [48]. Synthesis of hexakis(1-dodecynylphenyl)-peri-hexabenzocoronene (34a) as a representative example; 3.5.4 Synthesis of C96-C12 precursor 1,3,5-tris[3 ́,4 ́-di(4 ́ ́-dodecylphenyl)-2 ́,5 ́-diphenylphenyl]benzene (44a) by Diels-Alder cycloaddition reaction - a representative procedure for the synthesis of branched oligophenylenes [50]
3.5.5 Hydrogenation of hexakis-dodecyl-peri-hexabenzocoronenes 74 [66]
Record Nr. UNINA-9910877419303321
Weinheim, : Wiley-VCH
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Catalyzed carbon-heteroatom bond formation [[electronic resource] /] / edited by Andrei K. Yudin
Catalyzed carbon-heteroatom bond formation [[electronic resource] /] / edited by Andrei K. Yudin
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (523 p.)
Disciplina 546.6812
Altri autori (Persone) YudinAndrei K
Soggetto topico Carbon compounds
Chemical bonds
Soggetto genere / forma Electronic books.
ISBN 3-527-63340-5
1-282-84957-3
9786612849572
3-527-63338-3
3-527-63339-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 1.3.5 Pd-Catalyzed Carboamination Reactions of Alkynes, Allenes, and Dienes1.3.6 Vicinal Difunctionalization of Alkenes and Allenes; 1.4 Synthesis of Nitrogen Heterocycles via Intermediate π-Allylpalladium Complexes; 1.4.1 Reactions Involving Oxidative Addition of Allylic Electrophiles; 1.4.2 Reactions Involving π-Allylpalladium Intermediates Generated via Alkene Carbopalladation; 1.4.3 Reactions Involving Aminopalladation of 1,3-Dienes; 1.4.4 Generation of Allylpalladium Intermediates through C-H Activation
2.5.2 Reductive Cyclization of Ketoacids and Ketoesters2.5.3 C-H Oxygenation; 2.5.4 Ring Closure of Benzoic Acids with Dihaloalkanes; 2.5.5 Baeyer-Villiger Oxidation of Cyclic Ketones; 2.5.6 Ring Opening of Cyclopropanes with Carboxylic Acids; 2.5.7 Ring Closure of o-Iodobenzoates with Aldehydes; 2.5.8 Synthesis of Lactones Involving CO2; 2.5.9 Michael Addition of α,β-Unsaturated N-Acylpyrrolidines; 2.5.10 [2 + 2] Cycloaddition of Ketenes and Aldehydes; 2.5.11 Tandem Cross-Metathesis/Hydrogenation Route to Lactones; 2.5.12 Modern Catalytic Variants of Classical Macrolactonizations
2.6 Conclusions and Outlook
Record Nr. UNINA-9910140759103321
Weinheim, Germany, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
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