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Aromatic polyethers based on heterocyclic monomers [[electronic resource] /] / Alexander L. Rusanov and Nataliya M. Belomoina ; G. E. Zaikov, editor
| Aromatic polyethers based on heterocyclic monomers [[electronic resource] /] / Alexander L. Rusanov and Nataliya M. Belomoina ; G. E. Zaikov, editor |
| Autore | Rusanov A. L (Aleksandr Lvovich), <1939-> |
| Pubbl/distr/stampa | New York, : Novinka/Nova Science Publishers, c2011 |
| Descrizione fisica | 1 online resource (179 p.) |
| Disciplina | 668.4/23 |
| Altri autori (Persone) | BelmoinaN. M |
| Collana | Chemistry research applications |
| Soggetto topico |
Polyethers - Synthesis
Aromatic compounds - Synthesis Monomers Heterocyclic compounds |
| Soggetto genere / forma | Electronic books. |
| ISBN | 1-61122-170-6 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910457761303321 |
Rusanov A. L (Aleksandr Lvovich), <1939->
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| New York, : Novinka/Nova Science Publishers, c2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Aromatic polyethers based on heterocyclic monomers [[electronic resource] /] / Alexander L. Rusanov and Nataliya M. Belomoina ; G. E. Zaikov, editor
| Aromatic polyethers based on heterocyclic monomers [[electronic resource] /] / Alexander L. Rusanov and Nataliya M. Belomoina ; G. E. Zaikov, editor |
| Autore | Rusanov A. L (Aleksandr Lvovich), <1939-> |
| Pubbl/distr/stampa | New York, : Novinka/Nova Science Publishers, c2011 |
| Descrizione fisica | 1 online resource (179 p.) |
| Disciplina | 668.4/23 |
| Altri autori (Persone) | BelmoinaN. M |
| Collana | Chemistry research applications |
| Soggetto topico |
Polyethers - Synthesis
Aromatic compounds - Synthesis Monomers Heterocyclic compounds |
| ISBN | 1-61122-170-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910781850803321 |
|
Rusanov A. L (Aleksandr Lvovich), <1939->
|
||
| New York, : Novinka/Nova Science Publishers, c2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Aromatic polyethers based on heterocyclic monomers / / Alexander L. Rusanov and Nataliya M. Belomoina ; G. E. Zaikov, editor
| Aromatic polyethers based on heterocyclic monomers / / Alexander L. Rusanov and Nataliya M. Belomoina ; G. E. Zaikov, editor |
| Autore | Rusanov A. L (Aleksandr Lvovich), <1939-> |
| Edizione | [First edition.] |
| Pubbl/distr/stampa | New York, : Novinka/Nova Science Publishers, c2011 |
| Descrizione fisica | 1 online resource (179 pages) |
| Disciplina | 668.4/23 |
| Altri autori (Persone) | BelmoinaN. M |
| Collana | Chemistry research applications |
| Soggetto topico |
Polyethers - Synthesis
Aromatic compounds - Synthesis Monomers Heterocyclic compounds |
| ISBN | 1-61122-170-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Intro -- Contents -- Introduction -- Activated Electrophilic Aromatic Compounds Containing Aromatic Heterocycles -- 2-1. Reactivity of Activated Electrophilic Aromatic Compounds Containing Aromatic Heterocycles -- 2-2. Synthesis and Properties of Electrophilic Aromatic Monomers Containing Aromatic Heterocycles -- 2-2-1. Electrophilic Aromatic Monomers Containing Azole and Benzazole Cycles -- 2-2-2. Electrophilic Aromatic Monomers Containing Azine and Benzazine Cycles -- 2-2-3. Electrophilic Aromatic Monomers Containing Imide Cycles -- Poly(Arylene Ethers) Containing Aromatic Heterocycles Based on Activated Electrophilic Monomers -- 3-1. Poly(Arylene Ethers) Based on Azole and Benzazole Containing Electrophilic Monomers -- 3-2. Poly(Arylene Ethers) Based on Azine and Benzazine Containing Electrophilic Monomers -- 3-3. Poly(Arylene Ethers) Based on Imide Containing Electrophilic Monomers -- 3-4. Aromatic Polyethers Based on Electrophilic Monomers Containing Heterocyclic Ortho-Activators -- Bisphenols Containing Heterocyclic Groups -- 4-1. Bisphenols Containing Azole and Benzazole Rings -- 4-2. Bisphenols Containing Azine and Benzanine Rings -- 4-3. Bisphenols Containing Imide and Highly Condensed Heterocycles -- Aromatic Polyethers Based on Bisphenols Containing -- Aromatic Heterocycles -- 5-1. Aromatic Polyethers Based on Bisphenols Containing Azole and Benzazole Rings -- 5-2. Aromatic Polyethers Based on Bisphenols Containing Azine and Benzazine Rings -- 5-3. Aromatic Polyethers Based on Bisphenols Containing Imide and Highly Condensed Rings -- Poly(Arylene Ethers) Containing Heterocyclic Units Prepared Using A-B Type Monomers -- Conclusions -- References -- Index -- Blank Page. |
| Record Nr. | UNINA-9910824543603321 |
|
Rusanov A. L (Aleksandr Lvovich), <1939->
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| New York, : Novinka/Nova Science Publishers, c2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Side reactions in organic synthesis II : aromatic substitutions / / Florencio Zaragoza Dörwald
| Side reactions in organic synthesis II : aromatic substitutions / / Florencio Zaragoza Dörwald |
| Autore | Dörwald Florencio Zaragoza |
| Edizione | [Second edition.] |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmbH & Co. KGaA, , [2014] |
| Descrizione fisica | 1 online resource (311 p.) |
| Disciplina | 547.6 |
| Soggetto topico |
Aromatic compounds - Synthesis
Organic compounds - Synthesis Aromatic compounds |
| ISBN |
3-527-68172-8
3-527-68780-7 3-527-68174-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Side Reactions in Organic Synthesis II; Contents; Preface; Glossary and Abbreviations; Journal Abbreviation List; Chapter 1 Electrophilic Alkylation of Arenes; 1.1 General Aspects; 1.1.1 Catalysis by Transition-Metal Complexes; 1.1.2 Typical Side Reactions; 1.2 Problematic Arenes; 1.2.1 Electron-Deficient Arenes; 1.2.2 Phenols; 1.2.3 Anilines; 1.2.4 Azoles; 1.3 Problematic Electrophiles; 1.3.1 Methylations; 1.3.2 Olefins; 1.3.3 Allylic Electrophiles; 1.3.4 Epoxides; 1.3.5 α-Haloketones and Related Electrophiles; 1.3.6 Nitroalkanes; 1.3.7 Ketones; 1.3.8 Alcohols; References
Chapter 2 Electrophilic Olefination of Arenes2.1 General Aspects; 2.2 Olefinations with Leaving-Group-Substituted Olefins; 2.3 Olefinations with Unsubstituted Olefins; 2.4 Olefinations with Alkynes; References; Chapter 3 Electrophilic Arylation of Arenes; 3.1 General Aspects; 3.2 Arylations with Aryl Halides; 3.2.1 Via Cationic Intermediates; 3.2.2 Via Radicals; 3.2.3 Via Transition-Metal Chelates; 3.2.4 By Transition-Metal Catalysis; 3.3 Arylations with Diazonium Salts; 3.4 Arylations with Other Functionalized Arenes; 3.5 Arylations with Unsubstituted Arenes; References Chapter 4 Electrophilic Acylation of Arenes4.1 General Aspects; 4.2 Problematic Arenes; 4.2.1 Dealkylation/Isomerization of Arenes; 4.2.2 Styrenes; 4.2.3 Anilines, Phenols, and Thiophenols; 4.2.4 Electron-Deficient Arenes; 4.2.5 Azoles; 4.3 Problematic Electrophiles; 4.3.1 Problematic Acyl Halides; 4.3.2 Carboxylic Esters and Lactones; 4.3.3 Carbonic Acid Derivatives; 4.3.4 Formic Acid Derivatives; 4.3.5 Mixed Carboxylic Anhydrides and Other Polyelectrophiles; References; Chapter 5 Electrophilic Halogenation of Arenes; 5.1 General Aspects; 5.2 Typical Side Reactions; 5.3 Regioselectivity 5.4 Catalysis5.5 Fluorinations; 5.6 Electron-Deficient Arenes; 5.6.1 Pyridines; 5.6.2 Benzoic Acid Derivatives; 5.7 Electron-Rich Arenes; 5.7.1 Phenols and Arylethers; 5.7.2 Anilines; 5.7.3 Azoles; 5.8 Sensitive Functional Groups; 5.8.1 Alkenes; 5.8.2 Amines; 5.8.3 Ethers; 5.8.4 Thiols and Thioethers; 5.8.5 Aldehydes, Ketones, and Other C-H Acidic Compounds; 5.8.6 Amides; References; Chapter 6 Electrophilic Formation of Aromatic C-N Bonds; 6.1 Nitration of Arenes; 6.1.1 Mechanisms; 6.1.2 Regioselectivity; 6.1.3 Catalysis; 6.1.4 Electron-Deficient Arenes; 6.1.5 Electron-Rich Arenes 6.1.5.1 Anilines6.1.5.2 Indoles; 6.1.5.3 Phenols; 6.2 Electrophilic Aromatic Aminations; 6.2.1 Typical Side Reactions; 6.3 Electrophilic Aromatic Amidations; 6.3.1 Typical Side Reactions; References; Chapter 7 Electrophilic Formation of Aromatic C-S Bonds; 7.1 Sulfonylation; 7.1.1 General Aspects; 7.1.2 Typical Side Reactions; 7.2 Sulfinylation; 7.2.1 General Aspects; 7.2.2 Typical Side Reactions; 7.3 Sulfenylation; 7.3.1 General Aspects; 7.3.2 Typical Side Reactions; References; Chapter 8 Aromatic Nucleophilic Substitutions; 8.1 General Aspects; 8.1.1 Mechanisms; 8.1.2 Regioselectivity 8.1.3 Acid-/Base-Catalysis |
| Altri titoli varianti |
Side reactions in organic synthesis 2
Side reactions in organic synthesis two |
| Record Nr. | UNINA-9910830571203321 |
|
Dörwald Florencio Zaragoza
|
||
| Weinheim, Germany : , : Wiley-VCH Verlag GmbH & Co. KGaA, , [2014] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Transition-metal-mediated aromatic ring construction [[electronic resource] /] / edited by Ken Tanaka
| Transition-metal-mediated aromatic ring construction [[electronic resource] /] / edited by Ken Tanaka |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, c2013 |
| Descrizione fisica | 1 online resource (831 p.) |
| Disciplina | 547/.6 |
| Altri autori (Persone) | TanakaKen <1967-> |
| Soggetto topico |
Aromatic compounds - Synthesis
Transition metal catalysts |
| ISBN |
1-118-62999-X
1-118-62987-6 1-118-63016-5 |
| Classificazione | SCI013040 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
TRANSITION-METAL-MEDIATEDAROMATIC RING CONSTRUCTION; CONTENTS; CONTRIBUTORS; PREFACE; PART I [2 + 2 + 2] AND RELATED CYCLOADDITION REACTIONS; 1 Cobalt-Mediated [2+2+2] Cycloaddition; 1.1 Introduction; 1.2 Synthesis of Benzenes; 1.2.1 New Catalytic Systems; 1.2.2 New Cyclization Partners; 1.2.3 Chemo- and Regioselectivity Issues; 1.3 Synthesis of Heterocycles; 1.3.1 New Catalytic Systems; 1.3.2 New Cyclization Partners; 1.3.3 Chemo- and Regioselectivity Issues; 1.4 Mechanistic Aspects; 1.5 Synthetic Applications; 1.5.1 Natural Products and Naturally Occurring Scaffolds; 1.5.2 Polyphenylenes
1.6 Summary and OutlookReferences; 2 Nickel-Mediated [2+2+2] Cycloaddition; 2.1 Introduction; 2.2 Synthesis of Benzenes; 2.3 Cycloaddition of Alkynes and Nitriles; 2.4 Cycloaddition of Alkynes and Imines; 2.5 Cycloaddition of Alkynes and Carbon Dioxide; 2.6 Cycloaddition of Alkynes and Isocyanates; 2.7 Cycloaddition of Alkynes and Carbodiimide; 2.8 Cycloaddition of Diynes and Ketenes; 2.9 Cycloaddition of Arynes; 2.10 Mechanism; 2.10.1 Coupling of Alkynes and Allene; 2.10.2 Cycloaddition of Alkyne and Nitrile; 2.10.3 Cycloaddition of Alkynes and Heterocumulenes; 2.10.4 Cycloaddition of Arynes 2.11 Summary and OutlookReferences; 3 Ruthenium-Mediated [2+2+2] Cycloaddition; 3.1 Introduction; 3.2 Synthesis of Benzenes; 3.2.1 Cyclotrimerization; 3.2.2 Cross-Cyclotrimerization; 3.2.3 Partially Intramolecular Cyclotrimerizations; 3.2.4 Fully Intramolecular Cyclotrimerization; 3.2.5 Cyclotrimerization of Alkynylboronates and 1-Haloalkynes; 3.3 Synthesis of Heterocycles; 3.3.1 Cyclocotrimerization of Alkynes with Nitriles to Form Pyridines; 3.3.2 Cyclocotrimerization of Alkynes with Heterocumulenes; 3.4 Mechanism of Ruthenium-Catalyzed [2+2+2] Cycloadditions; 3.5 Synthetic Applications 3.5.1 Synthesis of Biologically Interesting Molecules3.5.2 Synthesis of Polyaromatic Functional Molecules; 3.6 Summary and Outlook; References; 4 Rhodium-Mediated [2+2+2] Cycloaddition; 4.1 Introduction; 4.2 Synthesis of Benzenes; 4.2.1 Intermolecular Reactions Catalyzed by Neutral Rhodium Complexes; 4.2.2 Intermolecular Reactions Catalyzed by Cationic Rhodium Complexes; 4.2.3 Intramolecular Reactions Catalyzed by Neutral Rhodium Complexes; 4.2.4 Intramolecular Reactions Catalyzed by Cationic Rhodium Complexes; 4.3 Synthesis of Pyridines; 4.3.1 Intermolecular Reactions 4.3.2 Intramolecular Reactions4.4 Synthesis of Pyridones and Related Heterocycles; 4.4.1 Intermolecular Reactions; 4.4.2 Intramolecular Reactions; 4.5 Summary and Outlook; References; 5 Iridium-Mediated [2+2+2] Cycloaddition; 5.1 Introduction; 5.2 Synthesis of Benzene Derivatives; 5.3 Synthesis of Heterocyclic Compounds; 5.4 Mechanistic Aspects; 5.5 Summary and Outlook; References; 6 [2+2+2] and Related Cycloadditions Mediated by Other Transition Metals; 6.1 Introduction; 6.2 Palladium-Catalyzed [2+2+2] and [2+2+1] Cycloadditions; 6.2.1 [2+2+2] Cycloaddition; 6.2.2 [2+2+1] Cycloaddition 6.3 Iron-Catalyzed [2+2+2] Cycloaddition |
| Record Nr. | UNINA-9910141763303321 |
| Hoboken, N.J., : Wiley, c2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Transition-metal-mediated aromatic ring construction / / edited by Ken Tanaka
| Transition-metal-mediated aromatic ring construction / / edited by Ken Tanaka |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Hoboken, N.J., : Wiley, c2013 |
| Descrizione fisica | 1 online resource (831 p.) |
| Disciplina | 547/.6 |
| Altri autori (Persone) | TanakaKen <1967-> |
| Soggetto topico |
Aromatic compounds - Synthesis
Transition metal catalysts |
| ISBN |
1-118-62999-X
1-118-62987-6 1-118-63016-5 |
| Classificazione | SCI013040 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
TRANSITION-METAL-MEDIATEDAROMATIC RING CONSTRUCTION; CONTENTS; CONTRIBUTORS; PREFACE; PART I [2 + 2 + 2] AND RELATED CYCLOADDITION REACTIONS; 1 Cobalt-Mediated [2+2+2] Cycloaddition; 1.1 Introduction; 1.2 Synthesis of Benzenes; 1.2.1 New Catalytic Systems; 1.2.2 New Cyclization Partners; 1.2.3 Chemo- and Regioselectivity Issues; 1.3 Synthesis of Heterocycles; 1.3.1 New Catalytic Systems; 1.3.2 New Cyclization Partners; 1.3.3 Chemo- and Regioselectivity Issues; 1.4 Mechanistic Aspects; 1.5 Synthetic Applications; 1.5.1 Natural Products and Naturally Occurring Scaffolds; 1.5.2 Polyphenylenes
1.6 Summary and OutlookReferences; 2 Nickel-Mediated [2+2+2] Cycloaddition; 2.1 Introduction; 2.2 Synthesis of Benzenes; 2.3 Cycloaddition of Alkynes and Nitriles; 2.4 Cycloaddition of Alkynes and Imines; 2.5 Cycloaddition of Alkynes and Carbon Dioxide; 2.6 Cycloaddition of Alkynes and Isocyanates; 2.7 Cycloaddition of Alkynes and Carbodiimide; 2.8 Cycloaddition of Diynes and Ketenes; 2.9 Cycloaddition of Arynes; 2.10 Mechanism; 2.10.1 Coupling of Alkynes and Allene; 2.10.2 Cycloaddition of Alkyne and Nitrile; 2.10.3 Cycloaddition of Alkynes and Heterocumulenes; 2.10.4 Cycloaddition of Arynes 2.11 Summary and OutlookReferences; 3 Ruthenium-Mediated [2+2+2] Cycloaddition; 3.1 Introduction; 3.2 Synthesis of Benzenes; 3.2.1 Cyclotrimerization; 3.2.2 Cross-Cyclotrimerization; 3.2.3 Partially Intramolecular Cyclotrimerizations; 3.2.4 Fully Intramolecular Cyclotrimerization; 3.2.5 Cyclotrimerization of Alkynylboronates and 1-Haloalkynes; 3.3 Synthesis of Heterocycles; 3.3.1 Cyclocotrimerization of Alkynes with Nitriles to Form Pyridines; 3.3.2 Cyclocotrimerization of Alkynes with Heterocumulenes; 3.4 Mechanism of Ruthenium-Catalyzed [2+2+2] Cycloadditions; 3.5 Synthetic Applications 3.5.1 Synthesis of Biologically Interesting Molecules3.5.2 Synthesis of Polyaromatic Functional Molecules; 3.6 Summary and Outlook; References; 4 Rhodium-Mediated [2+2+2] Cycloaddition; 4.1 Introduction; 4.2 Synthesis of Benzenes; 4.2.1 Intermolecular Reactions Catalyzed by Neutral Rhodium Complexes; 4.2.2 Intermolecular Reactions Catalyzed by Cationic Rhodium Complexes; 4.2.3 Intramolecular Reactions Catalyzed by Neutral Rhodium Complexes; 4.2.4 Intramolecular Reactions Catalyzed by Cationic Rhodium Complexes; 4.3 Synthesis of Pyridines; 4.3.1 Intermolecular Reactions 4.3.2 Intramolecular Reactions4.4 Synthesis of Pyridones and Related Heterocycles; 4.4.1 Intermolecular Reactions; 4.4.2 Intramolecular Reactions; 4.5 Summary and Outlook; References; 5 Iridium-Mediated [2+2+2] Cycloaddition; 5.1 Introduction; 5.2 Synthesis of Benzene Derivatives; 5.3 Synthesis of Heterocyclic Compounds; 5.4 Mechanistic Aspects; 5.5 Summary and Outlook; References; 6 [2+2+2] and Related Cycloadditions Mediated by Other Transition Metals; 6.1 Introduction; 6.2 Palladium-Catalyzed [2+2+2] and [2+2+1] Cycloadditions; 6.2.1 [2+2+2] Cycloaddition; 6.2.2 [2+2+1] Cycloaddition 6.3 Iron-Catalyzed [2+2+2] Cycloaddition |
| Record Nr. | UNINA-9910816824503321 |
| Hoboken, N.J., : Wiley, c2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
