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Biblioteca

MARC Lista (tabellare)
Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Pubbl/distr/stampa Weinheim, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (659 p.)
Disciplina 547.59
547/.59
Altri autori (Persone) MajumdarKrishna C
ChattopadhyayShital K
Soggetto topico Heterocyclic compounds
Natural products - Synthesis
ISBN 3-527-63489-4
1-283-37054-9
9786613370549
3-527-63490-8
3-527-63488-6
Classificazione VK 5500
VK 7200
VK 8500
540
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Stained heterocyles in the synthesis of natural products -- pt. 2. Common ring heterocycles in natural product synthesis -- pt. 3. Natural products containing medium and large ring-sized heterocyclic systems.
Record Nr. UNINA-9910137853203321
Weinheim, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Heterocycles in natural product synthesis [[electronic resource] /] / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Pubbl/distr/stampa Weinheim, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (659 p.)
Disciplina 547.59
547/.59
Altri autori (Persone) MajumdarKrishna C
ChattopadhyayShital K
Soggetto topico Heterocyclic compounds
Natural products - Synthesis
ISBN 3-527-63489-4
1-283-37054-9
9786613370549
3-527-63490-8
3-527-63488-6
Classificazione VK 5500
VK 7200
VK 8500
540
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Stained heterocyles in the synthesis of natural products -- pt. 2. Common ring heterocycles in natural product synthesis -- pt. 3. Natural products containing medium and large ring-sized heterocyclic systems.
Record Nr. UNINA-9910830690903321
Weinheim, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Heterocycles in natural product synthesis / / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Heterocycles in natural product synthesis / / edited by Krishna C. Majumdar and Shital K. Chattopadhyay
Pubbl/distr/stampa Weinheim, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (659 p.)
Disciplina 547.59
547/.59
Altri autori (Persone) MajumdarKrishna C
ChattopadhyayShital K
Soggetto topico Heterocyclic compounds
Natural products - Synthesis
ISBN 3-527-63489-4
1-283-37054-9
9786613370549
3-527-63490-8
3-527-63488-6
Classificazione VK 5500
VK 7200
VK 8500
540
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Stained heterocyles in the synthesis of natural products -- pt. 2. Common ring heterocycles in natural product synthesis -- pt. 3. Natural products containing medium and large ring-sized heterocyclic systems.
Record Nr. UNINA-9910877349303321
Weinheim, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Terpyridine-based materials [[electronic resource] ] : for catalytic, optoelectronic and life science applications / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Terpyridine-based materials [[electronic resource] ] : for catalytic, optoelectronic and life science applications / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Autore Schubert U (Ulrich)
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (544 p.)
Disciplina 547.593
Altri autori (Persone) WinterAndreas
NewkomeGeorge R (George Richard)
Soggetto topico Pyridine
ISBN 3-527-63963-2
1-283-37057-3
9786613370570
3-527-63962-4
3-527-63964-0
Classificazione 540
VK 7150
VK 7200
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Terpyridine-based Materials: For Catalytic, Optoelectronic and Life Science Applications; Contents; Preface; List of Abbreviations; 1: Introduction; 2: Synthesis, Properties, and Applications of Functionalized 2,2 ;-Terpyridines; 2.1: Introduction; 2.2: Basic Synthetic Strategies; 2.2.1: Ring-Assembly Methodologies; 2.2.2: Cross-Coupling Procedures; 2.3: Synthesis and Properties of 2,-Terpyridine Derivatives; 2.3.1: 4x2032;-Substituted 2, Terpyridinoxy Derivatives; 2.3.2: Miscellaneous 4;-Substituted 2,2032;-Terpyridine Derivatives
3.3.1: Synthesis of RuII and OsII Bis(terpyridine) Complexes 3.3.2: RuII Ions and Terpyridine Ligands - A Happy Marriage?; 3.3.2.1: Photophysical Properties; 3.3.2.2: Mononuclear RuII Bis(terpyridine) Complexes; 3.3.2.3: Oligonuclear Complexes Containing RuII/OsII Bis(terpyridine) Units; 3.3.2.4: Dendritic and Star-Shaped Systems Containing RuII Bis(terpyridine) Units; 3.4: Iridium(III) Complexes with Terpyridine Ligands; 3.5: Platinum(II) Mono(terpyridine) Complexes; 4: Metallo-Supramolecular Architectures Based on Terpyridine Complexes; 4.1: Introduction
4.2: Terpyridine-Containing Metallo-Macrocycles 4.3: The HETTAP Concept; 4.4: Racks and Grids; 4.5: Helicates; 4.6: Rotaxanes and Catenanes; 4.7: Miscellaneous Structures; 4.7.1: Cyclodextrin Derivatives; 4.7.2: Other Assemblies; 5: CO; -Conjugated Polymers Incorporating Terpyridine Metal Complexes; 5.1: Introduction; 5.2: Metallo-Supramolecular Polymerization; 5.3: Metallopolymers Based on CO; -Conjugated Bis(terpyridine)s; 5.3.1: Polymerization by Transition Metal Ion Coordination; 5.3.2: Self-Assembly of Metallopolymers; 5.3.3: Chiral Metallopolymers; 5.3.4: Non-Classical Metallopolymers
5.3.5: Polymerization Using the ''Complex First'' Method 5.4: Main-Chain Metallopolymers Based on Terpyridine-Functionalized CO; -Conjugated Polymers; 6: Functional Polymers Incorporating Terpyridine-Metal Complexes; 6.1: Introduction; 6.2: Polymers with Terpyridine Units in the Side-Chain; 6.2.1: Materials Based on Flexible Organic Polymers; 6.2.2: Materials Based on CO; -Conjugated Polymers; 6.3: Polymers with Terpyridines within the Polymer Backbone; 6.3.1: Polymers from Organic Small-Molecule Building Blocks; 6.3.2: Chain-Extended Polymers from Polymeric Building Blocks
6.3.3: Monotopic Macroligands by End-Group Functionalization
Record Nr. UNINA-9910139742503321
Schubert U (Ulrich)  
Weinheim, Germany, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Terpyridine-based materials : for catalytic, optoelectronic and life science applications / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Terpyridine-based materials : for catalytic, optoelectronic and life science applications / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Autore Schubert U (Ulrich)
Edizione [1st ed.]
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (544 p.)
Disciplina 547.593
Altri autori (Persone) WinterAndreas
NewkomeGeorge R (George Richard)
Soggetto topico Pyridine
ISBN 3-527-63963-2
1-283-37057-3
9786613370570
3-527-63962-4
3-527-63964-0
Classificazione 540
VK 7150
VK 7200
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Terpyridine-based Materials: For Catalytic, Optoelectronic and Life Science Applications; Contents; Preface; List of Abbreviations; 1: Introduction; 2: Synthesis, Properties, and Applications of Functionalized 2,2 ;-Terpyridines; 2.1: Introduction; 2.2: Basic Synthetic Strategies; 2.2.1: Ring-Assembly Methodologies; 2.2.2: Cross-Coupling Procedures; 2.3: Synthesis and Properties of 2,-Terpyridine Derivatives; 2.3.1: 4x2032;-Substituted 2, Terpyridinoxy Derivatives; 2.3.2: Miscellaneous 4;-Substituted 2,2032;-Terpyridine Derivatives
3.3.1: Synthesis of RuII and OsII Bis(terpyridine) Complexes 3.3.2: RuII Ions and Terpyridine Ligands - A Happy Marriage?; 3.3.2.1: Photophysical Properties; 3.3.2.2: Mononuclear RuII Bis(terpyridine) Complexes; 3.3.2.3: Oligonuclear Complexes Containing RuII/OsII Bis(terpyridine) Units; 3.3.2.4: Dendritic and Star-Shaped Systems Containing RuII Bis(terpyridine) Units; 3.4: Iridium(III) Complexes with Terpyridine Ligands; 3.5: Platinum(II) Mono(terpyridine) Complexes; 4: Metallo-Supramolecular Architectures Based on Terpyridine Complexes; 4.1: Introduction
4.2: Terpyridine-Containing Metallo-Macrocycles 4.3: The HETTAP Concept; 4.4: Racks and Grids; 4.5: Helicates; 4.6: Rotaxanes and Catenanes; 4.7: Miscellaneous Structures; 4.7.1: Cyclodextrin Derivatives; 4.7.2: Other Assemblies; 5: CO; -Conjugated Polymers Incorporating Terpyridine Metal Complexes; 5.1: Introduction; 5.2: Metallo-Supramolecular Polymerization; 5.3: Metallopolymers Based on CO; -Conjugated Bis(terpyridine)s; 5.3.1: Polymerization by Transition Metal Ion Coordination; 5.3.2: Self-Assembly of Metallopolymers; 5.3.3: Chiral Metallopolymers; 5.3.4: Non-Classical Metallopolymers
5.3.5: Polymerization Using the ''Complex First'' Method 5.4: Main-Chain Metallopolymers Based on Terpyridine-Functionalized CO; -Conjugated Polymers; 6: Functional Polymers Incorporating Terpyridine-Metal Complexes; 6.1: Introduction; 6.2: Polymers with Terpyridine Units in the Side-Chain; 6.2.1: Materials Based on Flexible Organic Polymers; 6.2.2: Materials Based on CO; -Conjugated Polymers; 6.3: Polymers with Terpyridines within the Polymer Backbone; 6.3.1: Polymers from Organic Small-Molecule Building Blocks; 6.3.2: Chain-Extended Polymers from Polymeric Building Blocks
6.3.3: Monotopic Macroligands by End-Group Functionalization
Record Nr. UNINA-9910822310903321
Schubert U (Ulrich)  
Weinheim, Germany, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui