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Carbazole Derivatives : Latest Advances and Prospects / / Anna Caruso, editor
| Carbazole Derivatives : Latest Advances and Prospects / / Anna Caruso, editor |
| Pubbl/distr/stampa | [Place of publication not identified] : , : MDPI - Multidisciplinary Digital Publishing Institute, , 2023 |
| Descrizione fisica | 1 online resource (98 pages) |
| Disciplina | 547.59 |
| Soggetto topico |
Heterocyclic chemistry
Heterocyclic compounds |
| ISBN | 3-0365-7289-9 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Carbazole Derivatives |
| Record Nr. | UNINA-9910719771603321 |
| [Place of publication not identified] : , : MDPI - Multidisciplinary Digital Publishing Institute, , 2023 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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The chemistry of heterocycles [[electronic resource] ] : structure, reactions, synthesis, and applications / / Theophil Eicher, Siegfried Hauptmann, and Andreas Speicher
| The chemistry of heterocycles [[electronic resource] ] : structure, reactions, synthesis, and applications / / Theophil Eicher, Siegfried Hauptmann, and Andreas Speicher |
| Autore | Eicher Theophil |
| Edizione | [3rd, completely rev. and enl. ed.] |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2012 |
| Descrizione fisica | 1 online resource (648 p.) |
| Disciplina | 547.59 |
| Altri autori (Persone) |
HauptmannSiegfried
SpeicherAndreas |
| Soggetto topico | Heterocyclic chemistry |
| Soggetto genere / forma | Electronic books. |
| ISBN |
3-527-66986-8
1-299-31362-0 3-527-66987-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
The Chemistry of Heterocycles; Contents; Preface to the Third Edition; Abbreviations and Symbols; 1 The Structure of Heterocyclic Compounds; Reference; 2 Systematic Nomenclature of Heterocyclic Compounds; 2.1 Hantzsch-Widman Nomenclature; 2.2 Replacement Nomenclature; 2.3 Examples of Systematic Nomenclature; 2.4 Important Heterocyclic Systems; 3 Three-Membered Heterocycles; 3.1 Oxirane; 3.2 Thiirane; 3.3 2H-Azirine; 3.4 Aziridine; 3.5 Dioxirane; 3.6 Oxaziridine; 3.7 3H-Diazirine; 3.8 Diaziridine; References; 4 Four-Membered Heterocyles; 4.1 Oxetane; 4.2 Thietane; 4.3 Azete; 4.4 Azetidine
4.5 1,2-Dioxetane4.6 1,2-Dithiete; 4.7 1,2-Dihydro-1,2-diazete; 4.8 1,2-Diazetidine; References; 5 Five-Membered Heterocycles; 5.1 Furan; 5.2 Benzo[b]furan; 5.3 Isobenzofuran; 5.4 Dibenzofuran; 5.5 Tetrahydrofuran; 5.6 Thiophene; 5.7 Benzo[b]thiophene; 5.8 Benzo[c]thiophene; 5.9 2,5-Dihydrothiophene; 5.10 Thiolane; 5.11 Selenophene; 5.12 Pyrrole; 5.13 Indole; 5.14 Carbazole; 5.15 Isoindole; 5.16 Indolizine; 5.17 Pyrrolidine; 5.18 Phosphole; 5.19 1,3-Dioxolane; 5.20 1,2-Dithiole; 5.21 1,2-Dithiolane; 5.22 1,3-Dithiole; 5.23 1,3-Dithiolane; 5.24 Oxazole; 5.25 Benzoxazole 5.26 4,5-Dihydrooxazole5.27 Isoxazole; 5.28 4,5-Dihydroisoxazole; 5.29 2,3-Dihydroisoxazole; 5.30 Thiazole; 5.31 Benzothiazole; 5.32 Penam; 5.33 Isothiazole; 5.34 Imidazole; 5.35 Benzimidazole; 5.36 Imidazolidine; 5.37 Pyrazole; 5.38 Indazole; 5.39 4,5-Dihydropyrazole; 5.40 Pyrazolidine; 5.41 1,2,3-, 1,2,4-, 1,3,4-Oxadiazole; 5.42 1,2,5-Oxadiazole; 5.43 1,2,3-Thiadiazole; 5.44 1,2,4-Thiadiazole; 5.45 1,2,3-Triazole; 5.46 Benzotriazole; 5.47 1,2,4-Triazole; 5.48 Tetrazole; References; 6 Six-Membered Heterocycles; 6.1 Pyrylium Ion; 6.2 2H-Pyran; 6.3 2H-Pyran-2-one; 6.4 3,4-Dihydro-2H-pyran 6.5 Tetrahydropyran6.6 2H-Chromene; 6.7 2H-Chromen-2-one; 6.8 1-Benzopyrylium Ion; 6.9 4H-Pyran; 6.10 4H-Pyran-4-one; 6.11 4H-Chromene; 6.12 4H-Chromen-4-one; 6.13 Chroman; 6.14 Pyridine; 6.15 Pyridones; 6.16 Quinoline; 6.17 Isoquinoline; 6.18 Quinolizinium Ion; 6.19 Dibenzopyridines; 6.20 Piperidine; 6.21 Phosphabenzene; 6.22 1,4-Dioxin, 1,4-Dithiin, 1,4-Oxathiin; 6.23 1,4-Dioxane; 6.24 Oxazines; 6.25 Morpholine; 6.26 1,3-Dioxane; 6.27 1,3-Dithiane; 6.28 Cepham; 6.29 Pyridazine; 6.30 Pyrimidine; 6.31 Purine; 6.32 Pyrazine; 6.33 Piperazine; 6.34 Pteridine; 6.35 Benzodiazines 6.36 1,2,3-Triazine6.37 1,2,4-Triazine; 6.38 1,3,5-Triazine; 6.39 1,2,4,5-Tetrazine; References; 7 Seven-Membered Heterocycles; 7.1 Oxepin; 7.2 Thiepin; 7.3 Azepine; 7.4 Diazepines; References; 8 Larger Ring Heterocycles; 8.1 Azocine; 8.2 Heteronines and Larger-Membered Heterocycles; 8.3 Tetrapyrroles; References; 9 Problems and Their Solutions; References; Indices |
| Record Nr. | UNINA-9910465096003321 |
Eicher Theophil
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| Weinheim, : Wiley-VCH, c2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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The chemistry of heterocycles [[electronic resource] ] : structure, reactions, synthesis, and applications / / Theophil Eicher, Siegfried Hauptmann, and Andreas Speicher
| The chemistry of heterocycles [[electronic resource] ] : structure, reactions, synthesis, and applications / / Theophil Eicher, Siegfried Hauptmann, and Andreas Speicher |
| Autore | Eicher Theophil |
| Edizione | [3rd, completely rev. and enl. ed.] |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2012 |
| Descrizione fisica | xiii, 632 p. : ill |
| Disciplina | 547.59 |
| Altri autori (Persone) |
HauptmannSiegfried
SpeicherAndreas |
| Soggetto topico | Heterocyclic chemistry |
| ISBN |
3-527-66986-8
1-299-31362-0 3-527-66987-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910795976503321 |
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Eicher Theophil
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||
| Weinheim, : Wiley-VCH, c2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
The chemistry of heterocycles : structure, reactions, synthesis, and applications / / Theophil Eicher, Siegfried Hauptmann, and Andreas Speicher
| The chemistry of heterocycles : structure, reactions, synthesis, and applications / / Theophil Eicher, Siegfried Hauptmann, and Andreas Speicher |
| Autore | Eicher Theophil |
| Edizione | [3rd, completely rev. and enl. ed.] |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2012 |
| Descrizione fisica | xiii, 632 p. : ill |
| Disciplina | 547.59 |
| Altri autori (Persone) |
HauptmannSiegfried
SpeicherAndreas |
| Soggetto topico | Heterocyclic chemistry |
| ISBN |
3-527-66986-8
1-299-31362-0 3-527-66987-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Intro -- The Chemistry of Heterocycles -- Contents -- Preface to the Third Edition -- Abbreviations and Symbols -- 1 The Structure of Heterocyclic Compounds -- Reference -- 2 Systematic Nomenclature of Heterocyclic Compounds -- 2.1 Hantzsch-Widman Nomenclature -- 2.2 Replacement Nomenclature -- 2.3 Examples of Systematic Nomenclature -- 2.4 Important Heterocyclic Systems -- 3 Three-Membered Heterocycles -- 3.1 Oxirane -- 3.2 Thiirane -- 3.3 2H-Azirine -- 3.4 Aziridine -- 3.5 Dioxirane -- 3.6 Oxaziridine -- 3.7 3H-Diazirine -- 3.8 Diaziridine -- References -- 4 Four-Membered Heterocyles -- 4.1 Oxetane -- 4.2 Thietane -- 4.3 Azete -- 4.4 Azetidine -- 4.5 1,2-Dioxetane -- 4.6 1,2-Dithiete -- 4.7 1,2-Dihydro-1,2-diazete -- 4.8 1,2-Diazetidine -- References -- 5 Five-Membered Heterocycles -- 5.1 Furan -- 5.2 Benzo[b]furan -- 5.3 Isobenzofuran -- 5.4 Dibenzofuran -- 5.5 Tetrahydrofuran -- 5.6 Thiophene -- 5.7 Benzo[b]thiophene -- 5.8 Benzo[c]thiophene -- 5.9 2,5-Dihydrothiophene -- 5.10 Thiolane -- 5.11 Selenophene -- 5.12 Pyrrole -- 5.13 Indole -- 5.14 Carbazole -- 5.15 Isoindole -- 5.16 Indolizine -- 5.17 Pyrrolidine -- 5.18 Phosphole -- 5.19 1,3-Dioxolane -- 5.20 1,2-Dithiole -- 5.21 1,2-Dithiolane -- 5.22 1,3-Dithiole -- 5.23 1,3-Dithiolane -- 5.24 Oxazole -- 5.25 Benzoxazole -- 5.26 4,5-Dihydrooxazole -- 5.27 Isoxazole -- 5.28 4,5-Dihydroisoxazole -- 5.29 2,3-Dihydroisoxazole -- 5.30 Thiazole -- 5.31 Benzothiazole -- 5.32 Penam -- 5.33 Isothiazole -- 5.34 Imidazole -- 5.35 Benzimidazole -- 5.36 Imidazolidine -- 5.37 Pyrazole -- 5.38 Indazole -- 5.39 4,5-Dihydropyrazole -- 5.40 Pyrazolidine -- 5.41 1,2,3-, 1,2,4-, 1,3,4-Oxadiazole -- 5.42 1,2,5-Oxadiazole -- 5.43 1,2,3-Thiadiazole -- 5.44 1,2,4-Thiadiazole -- 5.45 1,2,3-Triazole -- 5.46 Benzotriazole -- 5.47 1,2,4-Triazole -- 5.48 Tetrazole -- References -- 6 Six-Membered Heterocycles.
6.1 Pyrylium Ion -- 6.2 2H-Pyran -- 6.3 2H-Pyran-2-one -- 6.4 3,4-Dihydro-2H-pyran -- 6.5 Tetrahydropyran -- 6.6 2H-Chromene -- 6.7 2H-Chromen-2-one -- 6.8 1-Benzopyrylium Ion -- 6.9 4H-Pyran -- 6.10 4H-Pyran-4-one -- 6.11 4H-Chromene -- 6.12 4H-Chromen-4-one -- 6.13 Chroman -- 6.14 Pyridine -- 6.15 Pyridones -- 6.16 Quinoline -- 6.17 Isoquinoline -- 6.18 Quinolizinium Ion -- 6.19 Dibenzopyridines -- 6.20 Piperidine -- 6.21 Phosphabenzene -- 6.22 1,4-Dioxin, 1,4-Dithiin, 1,4-Oxathiin -- 6.23 1,4-Dioxane -- 6.24 Oxazines -- 6.25 Morpholine -- 6.26 1,3-Dioxane -- 6.27 1,3-Dithiane -- 6.28 Cepham -- 6.29 Pyridazine -- 6.30 Pyrimidine -- 6.31 Purine -- 6.32 Pyrazine -- 6.33 Piperazine -- 6.34 Pteridine -- 6.35 Benzodiazines -- 6.36 1,2,3-Triazine -- 6.37 1,2,4-Triazine -- 6.38 1,3,5-Triazine -- 6.39 1,2,4,5-Tetrazine -- References -- 7 Seven-Membered Heterocycles -- 7.1 Oxepin -- 7.2 Thiepin -- 7.3 Azepine -- 7.4 Diazepines -- References -- 8 Larger Ring Heterocycles -- 8.1 Azocine -- 8.2 Heteronines and Larger-Membered Heterocycles -- 8.3 Tetrapyrroles -- References -- 9 Problems and Their Solutions -- References -- Indices. |
| Record Nr. | UNINA-9910961452403321 |
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Eicher Theophil
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||
| Weinheim, : Wiley-VCH, c2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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The Chemistry of Heterocyclic Compounds [[electronic resource] ] : Quinolines
| The Chemistry of Heterocyclic Compounds [[electronic resource] ] : Quinolines |
| Autore | Greenhill John V |
| Pubbl/distr/stampa | Hoboken, : Wiley, 2009 |
| Descrizione fisica | 1 online resource (578 p.) |
| Disciplina |
547.596
547/.59/05 |
| Collana | Chemistry of Heterocyclic Compounds: A Series Of Monographs |
| Soggetto topico |
Heterocyclic chemistry -- Periodicals
Heterocyclic chemistry Heterocyclic compounds -- Periodicals Heterocyclic compounds Quinoline Chemistry Organic Chemistry Physical Sciences & Mathematics |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-30181-0
9786612301810 0-470-18704-2 0-470-18857-X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | QUINOLINES; Contents; 1 Quinoline Aldehydes; 2 Quinoline Ketones; Author Index; Subject Index |
| Record Nr. | UNINA-9910144279903321 |
|
Greenhill John V
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| Hoboken, : Wiley, 2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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The Chemistry of Heterocyclic Compounds [[electronic resource] ] : Quinolines
| The Chemistry of Heterocyclic Compounds [[electronic resource] ] : Quinolines |
| Autore | Greenhill John V |
| Pubbl/distr/stampa | Hoboken, : Wiley, 2009 |
| Descrizione fisica | 1 online resource (578 p.) |
| Disciplina |
547.596
547/.59/05 |
| Collana | Chemistry of Heterocyclic Compounds: A Series Of Monographs |
| Soggetto topico |
Heterocyclic chemistry -- Periodicals
Heterocyclic chemistry Heterocyclic compounds -- Periodicals Heterocyclic compounds Quinoline Chemistry Organic Chemistry Physical Sciences & Mathematics |
| ISBN |
1-282-30181-0
9786612301810 0-470-18704-2 0-470-18857-X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | QUINOLINES; Contents; 1 Quinoline Aldehydes; 2 Quinoline Ketones; Author Index; Subject Index |
| Record Nr. | UNINA-9910830072103321 |
|
Greenhill John V
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||
| Hoboken, : Wiley, 2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Chemistry of pyrroles / / Boris A. Trofimov, Al'bina I. Mikhaleva, Elena Yu Schmidt, Lyubov N. Sobenina
| Chemistry of pyrroles / / Boris A. Trofimov, Al'bina I. Mikhaleva, Elena Yu Schmidt, Lyubov N. Sobenina |
| Pubbl/distr/stampa | Boca Raton : , : Taylor & Francis, , [2015] |
| Descrizione fisica | 1 online resource (394 p.) |
| Disciplina | 547.593 |
| Soggetto topico |
Pyrroles
Aromatic compounds Heterocyclic chemistry Chemistry, Organic |
| ISBN |
0-429-18582-0
1-4822-3243-X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Front Cover; Contents; Preface; Introduction; Chapter 1: Synthesis of Pyrroles and N-Vinylpyrroles by the Reaction of Ketones (Ketoximes) with Acetylenes; Chapter 2: Novel Aspects of NH- and N-Vinylpyrroles Reactivity; References; Back Cover |
| Record Nr. | UNINA-9910787840203321 |
| Boca Raton : , : Taylor & Francis, , [2015] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chemistry of pyrroles / / Boris A. Trofimov, Al'bina I. Mikhaleva, Elena Yu Schmidt, Lyubov N. Sobenina
| Chemistry of pyrroles / / Boris A. Trofimov, Al'bina I. Mikhaleva, Elena Yu Schmidt, Lyubov N. Sobenina |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Boca Raton : , : Taylor & Francis, , [2015] |
| Descrizione fisica | 1 online resource (394 p.) |
| Disciplina | 547.593 |
| Soggetto topico |
Pyrroles
Aromatic compounds Heterocyclic chemistry Chemistry, Organic |
| ISBN |
9781040218587
104021858X 9780429185823 0429185820 9781482232431 148223243X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Front Cover; Contents; Preface; Introduction; Chapter 1: Synthesis of Pyrroles and N-Vinylpyrroles by the Reaction of Ketones (Ketoximes) with Acetylenes; Chapter 2: Novel Aspects of NH- and N-Vinylpyrroles Reactivity; References; Back Cover |
| Record Nr. | UNINA-9910962495603321 |
| Boca Raton : , : Taylor & Francis, , [2015] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Current organic chemistry
| Current organic chemistry |
| Pubbl/distr/stampa | Hilversum, the Netherlands ; ; Miami, FL, : Bentham Science Publishers |
| Soggetto topico |
Chemistry, Organic
Asymmetric synthesis Organometallic chemistry Bioorganic chemistry Heterocyclic chemistry |
| ISSN | 1875-5348 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISA-996200976903316 |
| Hilversum, the Netherlands ; ; Miami, FL, : Bentham Science Publishers | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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Denitrogenative Transformation of Nitrogen Heterocycles : Synthesis, Reactions and Applications
| Denitrogenative Transformation of Nitrogen Heterocycles : Synthesis, Reactions and Applications |
| Autore | Anbarasan Pazhamalai |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Newark : , : John Wiley & Sons, Incorporated, , 2025 |
| Descrizione fisica | 1 online resource (537 pages) |
| Disciplina | 547.593 |
| Soggetto topico |
Heterocyclic chemistry
Nitrogen compounds |
| ISBN |
9783527844845
3527844848 9783527844838 352784483X 9783527844852 3527844856 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Title Page -- Copyright -- Contents -- Preface -- Chapter 1 Synthesis of Diverse Nitrogen Heterocycles Explored in Denitrogenative Transformations -- 1.1 Introduction -- 1.2 Synthesis of 1,2,3‐Triazoles -- 1.2.1 Synthesis of NH‐Triazoles -- 1.2.2 Synthesis of N‐Sulfonyl‐1,2,3‐triazoles -- 1.2.3 Synthesis of N‐Trifluoromethyl‐1,2,3‐triazoles -- 1.2.4 Synthesis of 5‐Iodo‐1,2,3‐triazoles -- 1.2.5 Synthesis of Pyridotriazoles -- 1.2.6 Synthesis of Triazoloindoles -- 1.2.7 Synthesis of Benzotriazoles -- 1.3 Synthesis of 1,2,3‐Thiadiazoles -- 1.4 Synthesis of Tetrazoles -- 1.4.1 Synthesis of 1H‐Tetrazoles -- 1.4.2 Synthesis of Pyridotetrazoles -- 1.4.3 Synthesis of Tetrazolo[1,5‐a]quinolines -- 1.5 Synthesis of 3‐Aminoindazoles -- 1.6 Synthesis of Benzotriazinones -- 1.7 Summary and Outlook -- References -- Chapter 2 Transannulation of N‐Sulfonyl‐1,2,3‐triazoles with Polar Multiple Bonds -- 2.1 Introduction -- 2.2 Reaction of N‐Sulfonyl‐1,2,3‐triazoles with Carbonyls -- 2.3 Reaction of N‐Sulfonyl‐1,2,3‐triazoles with Nitriles -- 2.4 Reaction of N‐Sulfonyl‐1,2,3‐triazoles with Polar Multiple Bonds Beyond Carbonyls and Nitriles -- 2.5 Conclusion -- References -- Chapter 3 Transannulation of N‐Sulfonyl‐1,2,3‐triazoles with Nonpolar Multiple Bonds such as Alkenes, Alkynes, and Allenes -- 3.1 Introduction -- 3.2 Transannulation of N‐Sulfonyl‐1,2,3‐triazoles with Alkenes -- 3.2.1 Intermolecular Transannulation with Alkenes -- 3.2.2 Intramolecular Transannulation with Alkenes -- 3.3 Transannulation of N‐Sulfonyl‐1,2,3‐triazoles with 1,3‐Dienes -- 3.3.1 Intermolecular Transannulation with 1,3‐Dienes -- 3.3.2 Intramolecular Transannulation with 1,3‐Dienes -- 3.4 Transannulation of N‐Sulfonyl‐1,2,3‐triazoles with Alkynes -- 3.4.1 Intermolecular Transannulation with Alkynes -- 3.4.2 Intramolecular Transannulation with Alkynes.
3.5 Transannulation of N‐Sulfonyl‐1,2,3‐triazoles with Allenes -- 3.5.1 Intermolecular Transannulation with Allenes -- 3.5.2 Intramolecular Transannulation with Allenes -- 3.6 Summary and Outlook -- References -- Chapter 4 Transannulations of N‐Sulfonyl‐1,2,3‐triazoles with Carbo/Heterocycles -- 4.1 Introduction -- 4.2 Transannulations with Ring Retention -- 4.2.1 Aromatic and Heteroaromatic Rings -- 4.2.2 Nonaromatic Rings -- 4.3 Transannulations with Ring Opening -- 4.3.1 Heteroaromatic Rings -- 4.3.2 Nonaromatic Rings -- 4.4 Summary and Outlook -- References -- Chapter 5 Insertion of Azavinyl Carbenes to C H/X H Bond -- 5.1 Abbreviations -- 5.2 Introduction -- 5.3 Insertion Reactions of N1‐Sulfonyl‐1,2,3‐triazoles -- 5.3.1 C-H Insertion -- 5.3.2 O-H Insertion -- 5.3.3 N-H Insertion -- 5.3.4 B-H Insertion -- 5.3.5 Si-H and P-H Insertion -- 5.4 Insertion Reactions of 5‐Iodo‐1,2,3‐triazoles -- 5.5 Summary and Outlook -- Acknowledgment -- References -- Chapter 6 Insertion of Azavinyl Carbenes to C X/X X Bond -- 6.1 Introduction -- 6.2 1,3‐Difunctionalization -- 6.3 [2,3]‐Sigmatropic Rearrangement Reactions -- 6.4 Insertion into X X bonds -- 6.5 Conclusion -- References -- Chapter 7 Denitrogenative Rearrangements of N‐Sulfonyl‐1,2,3‐triazoles -- 7.1 Introduction to Carbenes -- 7.2 Metal Carbenoids -- 7.3 Metal Carbenoids Derived from Diazo Compounds -- 7.4 α‐Imino Metal Carbenoids and Their Reactivity -- 7.5 Denitrogenative Rearrangements of N‐Sulfonyl‐1,2,3‐triazoles Through Azadiene Formation -- 7.6 Denitrogenative Rearrangements of N‐Sulfonyl‐1,2,3‐triazoles Through Zwitterionic Intermediate -- 7.7 Denitrogenative Rearrangements of N‐Sulfonyl‐1,2,3‐triazoles Through Ylide Formation -- 7.8 Denitrogenative Rearrangements of N‐Sulfonyl‐1,2,3‐triazoles Through Ketenimine Formation -- 7.9 Conclusion -- Acknowledgments -- References. Chapter 8 Denitrogenative Transformations of NH‐ and N‐Fluoroalkyl‐1,2,3‐triazoles -- 8.1 Introduction -- 8.2 Denitrogenation of NH‐1,2,3‐Triazoles -- 8.3 Denitrogenation of N‐Fluoroalkyl‐1,2,3‐triazoles -- 8.4 Summary and Outlook -- Acknowledgments -- References -- Chapter 9 Asymmetric Perspective on Denitrogenative Transformation of 1,2,3‐Triazoles -- 9.1 Introduction -- 9.2 Rhodium‐Catalyzed Cyclopropanation Reactions -- 9.3 Rhodium‐Catalyzed C H Insertion Reactions -- 9.4 Rhodium‐Catalyzed Transannulation Reactions -- 9.5 Miscellaneous Reactions -- 9.5.1 Relay Catalysis -- 9.5.2 Atom Transfer Reactions -- 9.6 Application in Natural Product and Total Synthesis -- 9.7 Summary and Outlook -- Acknowledgments -- References -- Chapter 10 Denitrogenative Transformations of 3‐Diazoindolin‐2‐imines -- 10.1 Introduction -- 10.2 Synthesis of 3‐Diazoindolin‐2‐imines -- 10.3 Insertion Reactions of 3‐Diazoindolin‐2‐imines -- 10.3.1 Insertion into X-H Bonds -- 10.3.2 Insertion into C-H Bonds -- 10.3.3 Insertion into C-X Bonds -- 10.4 Annulation Reactions of 3‐Diazoindolin‐2‐imines -- 10.5 Miscellaneous Reactions -- 10.6 Summary and Outlook -- References -- Chapter 11 Metal‐Catalyzed Denitrogenative Transformations of Pyridotriazoles -- 11.1 Introduction -- 11.2 Rhodium‐Catalyzed Transannulation of Pyridotriazoles -- 11.2.1 Rhodium‐Catalyzed Transannulation of Pyridotriazoles with Alkyl Silane, Alkynes, and Nitriles -- 11.2.2 Rhodium‐Catalyzed Transannulation of Pyridotriazoles with Amine and Amides -- 11.2.3 Rhodium‐Catalyzed [4 + 3] Cycloaddition of Pyridotriazoles with 2‐Phenylpyridine and S‐Aryl Sulfoximines -- 11.2.4 Rhodium‐Catalyzed Transannulation of Pyridotriazoles with 1,3‐Dienes -- 11.2.5 Rhodium‐Catalyzed Transannulation of Pyridotriazoles with N‐Phenylbenzimidamides. 11.2.6 Rhodium‐Catalyzed [4 + 1] Cycloaddition of Pyridotriazoles with Propargyl Alcohols -- 11.3 Palladium‐Catalyzed Ring‐Opening of [1,2,3]Triazolo[1,5‐a]pyridines -- 11.3.1 Palladium‐Catalyzed Ring‐Opening of Pyridotriazole with Aryl Halides -- 11.3.2 Palladium‐Catalyzed Ring‐Opening of Pyridotriazole with Acetic Anhydride -- 11.4 Copper‐Catalyzed Denitrogenative Transannulation of Pyridotriazoles -- 11.4.1 Copper‐Catalyzed Transannulation of Pyridotriazoles with Alkynes -- 11.4.2 Copper‐Catalyzed Transannulation of Pyridotriazoles with Amines and Amino Acids -- 11.5 Cobalt‐Catalyzed Transannulation of Pyridotriazoles with Isothiocyanates and Xanthate Esters -- 11.6 Ruthenium‐Catalyzed Transannulation of Pyridotriazoles with Naphthoquinones -- 11.7 Summary and Conclusion -- Acknowledgments -- References -- Chapter 12 Metal‐Free Denitrogenative Transformation of Pyridotriazoles -- 12.1 Introduction -- 12.2 Acid‐Catalyzed Denitrogenative Transformation of Pyridotriazoles -- 12.2.1 Lewis‐Acid Catalyzed Reactions -- 12.2.2 Brønsted Acid‐Catalyzed Reactions -- 12.3 Denitrogenative Transformations of Pyridotriazoles for Forming C C and C X Bond -- 12.3.1 Coupling of Boronic Acids with Pyridotriazoles -- 12.3.2 Iodine and Bromine Promoted Transformations of Pyridotriazoles -- 12.4 Thermolysis and Photolysis of Pyridotriazoles -- 12.5 Light‐Induced Transformations of Pyridotriazoles -- 12.6 Summary and Outlook -- Acknowledgments -- References -- Chapter 13 Recent Development in Denitrogenative Transannulation of Benzotriazoles -- 13.1 Introduction -- 13.2 Common Route for the Synthesis of Benzotriazole Precursors -- 13.3 Transannulation of Benzotriazole‐Appended Scaffolds -- 13.4 Conclusions and Future Perspective -- Acknowledgments -- References -- Chapter 14 Denitrogenative Transannulation of Thiadiazoles -- 14.1 Introduction. 14.2 Rh‐Catalyzed Reaction of 1,2,3‐Thiadiazoles with Alkynes -- 14.2.1 Rh‐Catalyzed Thiavinyl Carbenes from 1,2,3‐Thiadiazoles for the Synthesis of Multisubstituted Thiophenes -- 14.2.2 Rh‐Catalyzed Intramolecular Transannulation Reaction of Alkynyl Thiadiazoles for the Synthesis of 5,n‐fused Thiophenes -- 14.2.3 Rh‐Catalyzed Denitrogenative Transformations of 1,2,3‐Thiadiazoles for the Synthesis of Multisubstituted Furans and Thiophenes -- 14.2.4 Rh‐Catalyzed 1,1‐Hydroacylation of Thioacyl Carbenes with Alkynyl Aldehydes and Subsequent Cyclization for the Synthesis of 4H‐Thiopyran‐4‐ones -- 14.3 Rh‐Catalyzed Reaction of 1,2,3‐Thiadiazoles with Alkenes -- 14.3.1 Regioselective Synthesis of Dihydrothiophenes and Thiophenes via the Rh‐Catalyzed Transannulation of 1,2,3‐Thiadiazoles with Alkenes -- 14.3.2 Ir‐Catalyzed Diastereospecific and Enantioselective (3 + 2) Transannulations of 1,2,3‐Thiadiazoles with Norbornenes -- 14.3.3 Rh‐Catalyzed 1,1‐Hydroacylation of Thioacyl Carbenes with Alkynyl Aldehydes and Subsequent Cyclization -- 14.4 Rh‐Catalyzed Reaction of 1,2,3‐Thiadiazoles with Carbonyl Compounds -- 14.4.1 Ag‐Mediated Annulation of 5H‐1,2,3‐Thiadiazoles with 1,3‐Dicarbonyls for the Synthesis of Polysubstituted Furans -- 14.5 Rh‐Catalyzed Reaction of 1,2,3‐Thiadiazoles with Nitriles -- 14.5.1 Rh‐Catalyzed Transannulation of 1,2,3‐Thiadiazoles with Nitriles for the Synthesis of Isothiazole -- 14.5.2 Synthesis of Bicyclic Isothiazoles via Intramolecular Rh‐Catalyzed Transannulation of Cyanothiadiazoles -- 14.5.3 Rh‐Catalyzed Highly Chemoselective and Diastereoselective (3 + 2) Transannulations of 1,2,3‐Thiadiazoles with Cyanoepoxides -- 14.5.4 Transannulaction of 1,2,3‐Thiadiazoles and Alk‐2‐enenitriles for the Synthesis of 3‐(Alk‐1‐enyl)isothiazoles -- 14.6 Rh‐Catalyzed Reaction of 1,2,3‐Thiadiazoles with Imines. 14.6.1 (2 + 2 + 2) Annulations of Thioketenes and Imines. |
| Record Nr. | UNINA-9911020463603321 |
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Anbarasan Pazhamalai
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| Newark : , : John Wiley & Sons, Incorporated, , 2025 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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