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13 CNMR data for organometallic compounds / Brian E. Mann, Brian F. Taylor
13 CNMR data for organometallic compounds / Brian E. Mann, Brian F. Taylor
Autore MANN, Brian E.
Pubbl/distr/stampa London : Academic Press, 1981
Descrizione fisica VIII, 326 p. : ill. graf. tab. ; 23 cm
Disciplina 547.05
Altri autori (Persone) TAYLOR, Brian F.
Collana Organometallic chemistry. A series of monographs
Soggetto topico Spettroscopia
Chimica fisica organica
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISA-990003298640203316
MANN, Brian E.  
London : Academic Press, 1981
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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1: Historical Development and Essential Features / D. Michael, P. Mingos editors
1: Historical Development and Essential Features / D. Michael, P. Mingos editors
Pubbl/distr/stampa Cham, : Springer, 2019
Descrizione fisica XI, 265 p. : ill. ; 24 cm
Disciplina 540(Chimica generale)
546(Chimica inorganica)
615.19(Chimica farmaceutica. Tecnologia farmaceutica. Chimica medica)
541.395(Catalisi)
547.05(Chimica dei composti metallorganici)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-VAN0127233
Cham, : Springer, 2019
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
1: Historical Development and Essential Features / D. Michael, P. Mingos editors
1: Historical Development and Essential Features / D. Michael, P. Mingos editors
Pubbl/distr/stampa Cham, : Springer, 2019
Descrizione fisica XI, 265 p. : ill. ; 24 cm
Disciplina 540(Chimica generale)
546(Chimica inorganica)
615.19(Chimica farmaceutica. Tecnologia farmaceutica. Chimica medica)
541.395(Catalisi)
547.05(Chimica dei composti metallorganici)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-VAN00127233
Cham, : Springer, 2019
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
1: Historical Development and Essential Features / D. Michael, P. Mingos editors
1: Historical Development and Essential Features / D. Michael, P. Mingos editors
Edizione [Cham : Springer, 2019]
Pubbl/distr/stampa XI, 265 p., : ill. ; 24 cm
Descrizione fisica Pubblicazione in formato elettronico
Disciplina 540(Chimica generale)
546(Chimica inorganica)
615.19(Chimica farmaceutica. Tecnologia farmaceutica)
541.395(Catalisi)
547.05(Chimica dei composti metallorganici)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-SUN0127233
XI, 265 p., : ill. ; 24 cm
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
2: Catalytic, Materials, Biological and Medical Applications / D. Michael, P. Mingos editors
2: Catalytic, Materials, Biological and Medical Applications / D. Michael, P. Mingos editors
Pubbl/distr/stampa Cham, : Springer, 2019
Descrizione fisica XI, 242 p. : ill. ; 24 cm
Disciplina 540(Chimica generale)
546(Chimica inorganica)
615.19(Chimica farmaceutica. Tecnologia farmaceutica. Chimica medica)
541.395(Catalisi)
547.05(Chimica dei composti metallorganici)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-VAN0127232
Cham, : Springer, 2019
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
2: Catalytic, Materials, Biological and Medical Applications / D. Michael, P. Mingos editors
2: Catalytic, Materials, Biological and Medical Applications / D. Michael, P. Mingos editors
Pubbl/distr/stampa Cham, : Springer, 2019
Descrizione fisica XI, 242 p. : ill. ; 24 cm
Disciplina 540(Chimica generale)
546(Chimica inorganica)
615.19(Chimica farmaceutica. Tecnologia farmaceutica. Chimica medica)
541.395(Catalisi)
547.05(Chimica dei composti metallorganici)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-VAN00127232
Cham, : Springer, 2019
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
2: Catalytic, Materials, Biological and Medical Applications / D. Michael, P. Mingos editors
2: Catalytic, Materials, Biological and Medical Applications / D. Michael, P. Mingos editors
Edizione [Cham : Springer, 2019]
Pubbl/distr/stampa XI, 242 p., : ill. ; 24 cm
Descrizione fisica Pubblicazione in formato elettronico
Disciplina 540(Chimica generale)
546(Chimica inorganica)
615.19(Chimica farmaceutica. Tecnologia farmaceutica)
541.395(Catalisi)
547.05(Chimica dei composti metallorganici)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-SUN0127232
XI, 242 p., : ill. ; 24 cm
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
Active metals [[electronic resource] ] : preparation, characterization, applications / / edited by Alois Fürstner
Active metals [[electronic resource] ] : preparation, characterization, applications / / edited by Alois Fürstner
Pubbl/distr/stampa Weinheim ; ; New York, : VCH, c1996
Descrizione fisica 1 online resource (486 p.)
Disciplina 546.3
547.05
Altri autori (Persone) FürstnerAlois
Soggetto topico Metal activation
Active metals
Organometallic compounds - Synthesis
Soggetto genere / forma Electronic books.
ISBN 1-281-75857-4
9786611758578
3-527-61517-2
3-527-61516-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Active Metals; Preface; Contents; List of Contributors; 1 Rieke Metals : Highly Reactive Metal Powders Prepared by Alkali Metal Reduction of Metal Salts; 1.1 Introduction; 1.1.1 Physical Characteristics of Highly Reactive Metal Powders; 1.2 Rieke Magnesium, Calcium, Strontium, and Barium; 1.2.1 Formation of Rieke Magnesium; 1.2.2 Formation of Rieke Calcium. Strontium. and Barium; 1.2.3 Grignard Reactions Using Rieke Metals; 1.2.4 1,3-Dicne-Magnesium Reagents; 1.2.4.1 Preparation; 1.2. 4.2 Regioselcctivity
1.2.4.3 Carbocyclization of (1.4-Diphenyl-2-butene-1,4-diyl)magnesium with Organic Dihalides1.2.4.4 1,2-Dimethylenecycloalkan e.Magnesium Reagents; 1.2.4.5 Synthesis of Fused Carbocycles, β, γ-Unsaturated Ketones and 3-Cyclopentenols from Conjugated Diene-Magnesium Reagents; 1.2.4.6 Synthesis of Spiro γ-Lactones and Spiro δ-Lactones from 1,3-Diene-Magnesium Reagents; 1.2.4.7 Synthesis of γ-Lactams from Conjugated Diene-Magnesium Reagents; 1.3 Rieke Zinc; 1.3.1 The Preparation of Rieke Zinc; 1.3.2 Direct Oxidative Addition of Functionalized Alkyl and Aryl Halides
1.3.3 Reactions of Organozinc Reagents with Acid Chlorides1.3.4 Reactions of Organozinc Reagents with α, β-Unsaturated Ketones; 1.3.5 Reactions with Allylic and Alkynyl Halides; 1.3.6 Cross-Coupling of Vinyl and Aryl Organozinc Reagents Using a Palladium Catalyst; 1.3.7 Intramolecular Cyclizations and Conjugate Additions Mediated by Rieke Zinc; 1.3.8 Formation of Tertiary and Secondary Alkylzinc Bromides; 1.3.9 Cyanide-Based Rieke Zinc; 1.4 Organocopper Reagents Utilizing Rieke Copper; 1.4.1 Introduction; 1.4.2 Background to the Development of Rieke Copper; 1.4.3 Phosphine-Based Copper
1.4.4 Lithium 2-Thienylcyanocuprate-Based Copper1.4.5 Copper Cyanide-Based Active Copper; 1.4.6 Two-Equivalent Reduction of Copper(I) Complexes : A Formal Copper Anion; 1.5 Rieke Aluminum, Indium, and Nickel; 1.5.1 Aluminum; 1.5.2 Indium; 1 5.3 Nickel; 1.6 Synthesis of Specialized Polymers and New Materials via Rieke Metals; 1.6.1 Formation of Polyarylenes Mediated by Rieke Zinc; 1.6.2 Regiocontrolled Synthesis of Poly(3-alkylthiophenes) and Related Polymers Mediated by Rieke Zinc; 1.6.3 Synthesis of Poly(phenylcarbyne) Mediated by Rieke Calcium, Strontium, or Barium
1.6.4 Chemical Modification of Halogenated Polystyrenes Using Rieke Calcium or Copper1.6.5 Polymer Supported Rieke Metal Reagents and their Applications in Organic Synthesis; 2 Allylic Barium Reagents; 2.1 Introduction; 2.2 Preparation of Stereochemically Homogeneous Allylic Barium Reagents; 2.2.1 Direct Insertion Method Using Reactive Barium; 2.2.2 Stereochemical Stability; 2.2.3 Silylation of Stereochemically Homogeneous Allylic Barium Reagents; 2.2.3.1 Procedure for Generation of Reactive Barium (Ba*); 2.2.3.2 Procedure for Protonation of the Geranyl Barium Reagent
2.2.3.3 Silylation of (E)-2-Decenylbarium Chloride
Record Nr. UNINA-9910144280903321
Weinheim ; ; New York, : VCH, c1996
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Active metals [[electronic resource] ] : preparation, characterization, applications / / edited by Alois Fürstner
Active metals [[electronic resource] ] : preparation, characterization, applications / / edited by Alois Fürstner
Pubbl/distr/stampa Weinheim ; ; New York, : VCH, c1996
Descrizione fisica 1 online resource (486 p.)
Disciplina 546.3
547.05
Altri autori (Persone) FürstnerAlois
Soggetto topico Metal activation
Active metals
Organometallic compounds - Synthesis
ISBN 1-281-75857-4
9786611758578
3-527-61517-2
3-527-61516-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Active Metals; Preface; Contents; List of Contributors; 1 Rieke Metals : Highly Reactive Metal Powders Prepared by Alkali Metal Reduction of Metal Salts; 1.1 Introduction; 1.1.1 Physical Characteristics of Highly Reactive Metal Powders; 1.2 Rieke Magnesium, Calcium, Strontium, and Barium; 1.2.1 Formation of Rieke Magnesium; 1.2.2 Formation of Rieke Calcium. Strontium. and Barium; 1.2.3 Grignard Reactions Using Rieke Metals; 1.2.4 1,3-Dicne-Magnesium Reagents; 1.2.4.1 Preparation; 1.2. 4.2 Regioselcctivity
1.2.4.3 Carbocyclization of (1.4-Diphenyl-2-butene-1,4-diyl)magnesium with Organic Dihalides1.2.4.4 1,2-Dimethylenecycloalkan e.Magnesium Reagents; 1.2.4.5 Synthesis of Fused Carbocycles, β, γ-Unsaturated Ketones and 3-Cyclopentenols from Conjugated Diene-Magnesium Reagents; 1.2.4.6 Synthesis of Spiro γ-Lactones and Spiro δ-Lactones from 1,3-Diene-Magnesium Reagents; 1.2.4.7 Synthesis of γ-Lactams from Conjugated Diene-Magnesium Reagents; 1.3 Rieke Zinc; 1.3.1 The Preparation of Rieke Zinc; 1.3.2 Direct Oxidative Addition of Functionalized Alkyl and Aryl Halides
1.3.3 Reactions of Organozinc Reagents with Acid Chlorides1.3.4 Reactions of Organozinc Reagents with α, β-Unsaturated Ketones; 1.3.5 Reactions with Allylic and Alkynyl Halides; 1.3.6 Cross-Coupling of Vinyl and Aryl Organozinc Reagents Using a Palladium Catalyst; 1.3.7 Intramolecular Cyclizations and Conjugate Additions Mediated by Rieke Zinc; 1.3.8 Formation of Tertiary and Secondary Alkylzinc Bromides; 1.3.9 Cyanide-Based Rieke Zinc; 1.4 Organocopper Reagents Utilizing Rieke Copper; 1.4.1 Introduction; 1.4.2 Background to the Development of Rieke Copper; 1.4.3 Phosphine-Based Copper
1.4.4 Lithium 2-Thienylcyanocuprate-Based Copper1.4.5 Copper Cyanide-Based Active Copper; 1.4.6 Two-Equivalent Reduction of Copper(I) Complexes : A Formal Copper Anion; 1.5 Rieke Aluminum, Indium, and Nickel; 1.5.1 Aluminum; 1.5.2 Indium; 1 5.3 Nickel; 1.6 Synthesis of Specialized Polymers and New Materials via Rieke Metals; 1.6.1 Formation of Polyarylenes Mediated by Rieke Zinc; 1.6.2 Regiocontrolled Synthesis of Poly(3-alkylthiophenes) and Related Polymers Mediated by Rieke Zinc; 1.6.3 Synthesis of Poly(phenylcarbyne) Mediated by Rieke Calcium, Strontium, or Barium
1.6.4 Chemical Modification of Halogenated Polystyrenes Using Rieke Calcium or Copper1.6.5 Polymer Supported Rieke Metal Reagents and their Applications in Organic Synthesis; 2 Allylic Barium Reagents; 2.1 Introduction; 2.2 Preparation of Stereochemically Homogeneous Allylic Barium Reagents; 2.2.1 Direct Insertion Method Using Reactive Barium; 2.2.2 Stereochemical Stability; 2.2.3 Silylation of Stereochemically Homogeneous Allylic Barium Reagents; 2.2.3.1 Procedure for Generation of Reactive Barium (Ba*); 2.2.3.2 Procedure for Protonation of the Geranyl Barium Reagent
2.2.3.3 Silylation of (E)-2-Decenylbarium Chloride
Record Nr. UNISA-996202138303316
Weinheim ; ; New York, : VCH, c1996
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Active metals [[electronic resource] ] : preparation, characterization, applications / / edited by Alois Fürstner
Active metals [[electronic resource] ] : preparation, characterization, applications / / edited by Alois Fürstner
Pubbl/distr/stampa Weinheim ; ; New York, : VCH, c1996
Descrizione fisica 1 online resource (486 p.)
Disciplina 546.3
547.05
Altri autori (Persone) FürstnerAlois
Soggetto topico Metal activation
Active metals
Organometallic compounds - Synthesis
ISBN 1-281-75857-4
9786611758578
3-527-61517-2
3-527-61516-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Active Metals; Preface; Contents; List of Contributors; 1 Rieke Metals : Highly Reactive Metal Powders Prepared by Alkali Metal Reduction of Metal Salts; 1.1 Introduction; 1.1.1 Physical Characteristics of Highly Reactive Metal Powders; 1.2 Rieke Magnesium, Calcium, Strontium, and Barium; 1.2.1 Formation of Rieke Magnesium; 1.2.2 Formation of Rieke Calcium. Strontium. and Barium; 1.2.3 Grignard Reactions Using Rieke Metals; 1.2.4 1,3-Dicne-Magnesium Reagents; 1.2.4.1 Preparation; 1.2. 4.2 Regioselcctivity
1.2.4.3 Carbocyclization of (1.4-Diphenyl-2-butene-1,4-diyl)magnesium with Organic Dihalides1.2.4.4 1,2-Dimethylenecycloalkan e.Magnesium Reagents; 1.2.4.5 Synthesis of Fused Carbocycles, β, γ-Unsaturated Ketones and 3-Cyclopentenols from Conjugated Diene-Magnesium Reagents; 1.2.4.6 Synthesis of Spiro γ-Lactones and Spiro δ-Lactones from 1,3-Diene-Magnesium Reagents; 1.2.4.7 Synthesis of γ-Lactams from Conjugated Diene-Magnesium Reagents; 1.3 Rieke Zinc; 1.3.1 The Preparation of Rieke Zinc; 1.3.2 Direct Oxidative Addition of Functionalized Alkyl and Aryl Halides
1.3.3 Reactions of Organozinc Reagents with Acid Chlorides1.3.4 Reactions of Organozinc Reagents with α, β-Unsaturated Ketones; 1.3.5 Reactions with Allylic and Alkynyl Halides; 1.3.6 Cross-Coupling of Vinyl and Aryl Organozinc Reagents Using a Palladium Catalyst; 1.3.7 Intramolecular Cyclizations and Conjugate Additions Mediated by Rieke Zinc; 1.3.8 Formation of Tertiary and Secondary Alkylzinc Bromides; 1.3.9 Cyanide-Based Rieke Zinc; 1.4 Organocopper Reagents Utilizing Rieke Copper; 1.4.1 Introduction; 1.4.2 Background to the Development of Rieke Copper; 1.4.3 Phosphine-Based Copper
1.4.4 Lithium 2-Thienylcyanocuprate-Based Copper1.4.5 Copper Cyanide-Based Active Copper; 1.4.6 Two-Equivalent Reduction of Copper(I) Complexes : A Formal Copper Anion; 1.5 Rieke Aluminum, Indium, and Nickel; 1.5.1 Aluminum; 1.5.2 Indium; 1 5.3 Nickel; 1.6 Synthesis of Specialized Polymers and New Materials via Rieke Metals; 1.6.1 Formation of Polyarylenes Mediated by Rieke Zinc; 1.6.2 Regiocontrolled Synthesis of Poly(3-alkylthiophenes) and Related Polymers Mediated by Rieke Zinc; 1.6.3 Synthesis of Poly(phenylcarbyne) Mediated by Rieke Calcium, Strontium, or Barium
1.6.4 Chemical Modification of Halogenated Polystyrenes Using Rieke Calcium or Copper1.6.5 Polymer Supported Rieke Metal Reagents and their Applications in Organic Synthesis; 2 Allylic Barium Reagents; 2.1 Introduction; 2.2 Preparation of Stereochemically Homogeneous Allylic Barium Reagents; 2.2.1 Direct Insertion Method Using Reactive Barium; 2.2.2 Stereochemical Stability; 2.2.3 Silylation of Stereochemically Homogeneous Allylic Barium Reagents; 2.2.3.1 Procedure for Generation of Reactive Barium (Ba*); 2.2.3.2 Procedure for Protonation of the Geranyl Barium Reagent
2.2.3.3 Silylation of (E)-2-Decenylbarium Chloride
Record Nr. UNINA-9910829863503321
Weinheim ; ; New York, : VCH, c1996
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui

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