Catalytic heterofunctionalization : from hydroanimation [i.e. hydroamination] to hydrozirconation |
Pubbl/distr/stampa | [Place of publication not identified], : Wiley VCH, 2001 |
Descrizione fisica | 1 online resource (300 pages) |
Disciplina | 547.1395 |
Soggetto topico |
Catalysis - Synthesis
Organic compounds Organic Chemistry Chemistry Physical Sciences & Mathematics |
Soggetto genere / forma | Electronic books. |
ISBN |
1-280-55759-1
9786610557592 3-527-60015-9 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Hydroboration, diboration, silylboration, and stannylboration / Norio Miyaura -- Metal-catalyzed hydroalumination reactions / Marc Dahlmann and Mark Lautens -- Asymmetric hydrosilylation / Jun Tang and Tamio Hayashi -- Catalytic hydroamination of unsaturated carbon-carbon bonds / J.J. Brunet and D. Neibecker -- Hydrophosphination and related reactions / Denyce K. Wicht and David S. Glueck -- O-H activation and addition to unsaturated systems / Kazuhide Tani and Yasutaka Kataoka -- Sulfur (and related elements)-X activation / Hitoshi Kuniyasu -- Hydrozirconation / Alain Igau. |
Record Nr. | UNINA-9910146248203321 |
[Place of publication not identified], : Wiley VCH, 2001 | ||
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Lo trovi qui: Univ. Federico II | ||
|
Catalytic heterofunctionalization : from hydroanimation [i.e. hydroamination] to hydrozirconation |
Pubbl/distr/stampa | [Place of publication not identified], : Wiley VCH, 2001 |
Descrizione fisica | 1 online resource (300 pages) |
Disciplina | 547.1395 |
Soggetto topico |
Catalysis - Synthesis
Organic compounds Organic Chemistry Chemistry Physical Sciences & Mathematics |
ISBN |
1-280-55759-1
9786610557592 3-527-60015-9 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Hydroboration, diboration, silylboration, and stannylboration / Norio Miyaura -- Metal-catalyzed hydroalumination reactions / Marc Dahlmann and Mark Lautens -- Asymmetric hydrosilylation / Jun Tang and Tamio Hayashi -- Catalytic hydroamination of unsaturated carbon-carbon bonds / J.J. Brunet and D. Neibecker -- Hydrophosphination and related reactions / Denyce K. Wicht and David S. Glueck -- O-H activation and addition to unsaturated systems / Kazuhide Tani and Yasutaka Kataoka -- Sulfur (and related elements)-X activation / Hitoshi Kuniyasu -- Hydrozirconation / Alain Igau. |
Record Nr. | UNINA-9910829910603321 |
[Place of publication not identified], : Wiley VCH, 2001 | ||
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Lo trovi qui: Univ. Federico II | ||
|
Catalytic heterofunctionalization : from hydroanimation [i.e. hydroamination] to hydrozirconation |
Pubbl/distr/stampa | [Place of publication not identified], : Wiley VCH, 2001 |
Descrizione fisica | 1 online resource (300 pages) |
Disciplina | 547.1395 |
Soggetto topico |
Catalysis - Synthesis
Organic compounds Organic Chemistry Chemistry Physical Sciences & Mathematics |
ISBN |
1-280-55759-1
9786610557592 3-527-60015-9 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Hydroboration, diboration, silylboration, and stannylboration / Norio Miyaura -- Metal-catalyzed hydroalumination reactions / Marc Dahlmann and Mark Lautens -- Asymmetric hydrosilylation / Jun Tang and Tamio Hayashi -- Catalytic hydroamination of unsaturated carbon-carbon bonds / J.J. Brunet and D. Neibecker -- Hydrophosphination and related reactions / Denyce K. Wicht and David S. Glueck -- O-H activation and addition to unsaturated systems / Kazuhide Tani and Yasutaka Kataoka -- Sulfur (and related elements)-X activation / Hitoshi Kuniyasu -- Hydrozirconation / Alain Igau. |
Record Nr. | UNINA-9910876783103321 |
[Place of publication not identified], : Wiley VCH, 2001 | ||
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Lo trovi qui: Univ. Federico II | ||
|
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 | ||
![]() | ||
Lo trovi qui: Univ. Federico II | ||
|
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 | ||
![]() | ||
Lo trovi qui: Univ. di Salerno | ||
|
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. | UNINA-9910830440803321 |
Weinheim ; ; New York, : VCH Publishers, c1995 | ||
![]() | ||
Lo trovi qui: Univ. Federico II | ||
|
Ferrocenes : 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. | UNINA-9910877171803321 |
Weinheim ; ; New York, : VCH Publishers, c1995 | ||
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Lo trovi qui: Univ. Federico II | ||
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Metallocenes : synthesis, reactivity, applications |
Pubbl/distr/stampa | [Place of publication not identified], : Wiley VCH, 1998 |
Disciplina | 547/.05 |
Soggetto topico |
Metallocenes
Organic Chemistry Chemistry Physical Sciences & Mathematics |
ISBN | 3-527-61954-2 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910144352803321 |
[Place of publication not identified], : Wiley VCH, 1998 | ||
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Lo trovi qui: Univ. Federico II | ||
|
Metallocenes : synthesis, reactivity, applications |
Pubbl/distr/stampa | [Place of publication not identified], : Wiley VCH, 1998 |
Disciplina | 547/.05 |
Soggetto topico |
Metallocenes
Organic Chemistry Chemistry Physical Sciences & Mathematics |
ISBN | 3-527-61954-2 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNISA-996197428003316 |
[Place of publication not identified], : Wiley VCH, 1998 | ||
![]() | ||
Lo trovi qui: Univ. di Salerno | ||
|
Metallocenes : synthesis, reactivity, applications |
Pubbl/distr/stampa | [Place of publication not identified], : Wiley VCH, 1998 |
Disciplina | 547/.05 |
Soggetto topico |
Metallocenes
Organic Chemistry Chemistry Physical Sciences & Mathematics |
ISBN | 3-527-61954-2 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910830317603321 |
[Place of publication not identified], : Wiley VCH, 1998 | ||
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Lo trovi qui: Univ. Federico II | ||
|