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Au-Catalyzed Synthesis and Functionalization of Heterocycles / / edited by Marco Bandini
| Au-Catalyzed Synthesis and Functionalization of Heterocycles / / edited by Marco Bandini |
| Edizione | [1st ed. 2016.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016 |
| Descrizione fisica | 1 online resource (VII, 289 p. 20 illus., 9 illus. in color.) |
| Disciplina | 547.05 |
| Collana | Topics in Heterocyclic Chemistry |
| Soggetto topico |
Organometallic chemistry
Carbohydrates Catalysis Organometallic Chemistry Carbohydrate Chemistry |
| ISBN | 3-319-35144-3 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Synthesis of oxygenated heterocyclic compounds via gold catalyzed functionalization of π-systems -- Gold catalyzed synthesis of nitrogen heterocyclic compounds by hydroamination reactions -- Synthesis of oxygenated and nitrogen-contained heterocycles bygold-catalyzed alkyne oxidation -- Synthesis of Heterocyclic compounds via gold-catalyzed enyne rearrangements -- C-H functionalization of heteroaromatics via gold catalysis -- Enantioselective gold catalyzed synthesis of heterocyclic compounds -- Gold catalysis in the synthesis of heterocyclic natural products. |
| Record Nr. | UNINA-9910254034603321 |
| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2016 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Catalytic asymmetric Friedel-Crafts alkylations [[electronic resource] /] / edited by Marco Bandini and Achille Umani-Ronchi ; with a foreword by George A. Olah
| Catalytic asymmetric Friedel-Crafts alkylations [[electronic resource] /] / edited by Marco Bandini and Achille Umani-Ronchi ; with a foreword by George A. Olah |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2009 |
| Descrizione fisica | 1 online resource (319 p.) |
| Disciplina | 547.21 |
| Altri autori (Persone) |
BandiniMarco
Umani-RonchiAchille |
| Soggetto topico |
Friedel-Crafts reaction
Chemistry, Organic |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-68346-2
9786612683466 3-527-62697-2 3-527-62698-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Catalytic Asymmetric Friedel-Crafts Alkylations; Foreword; Contents; Preface; List of Contributors; 1 General Aspects and Historical Background; 1.1 Introduction; 1.2 General Aspects and Historical Background; 1.3 Catalytic Enantioselective FC Reactions: An Introduction; 1.3.1 Alkylating Agents; 1.3.2 Privileged Catalysts; 1.3.3 Aromatic Compounds and Reaction Conditions; References; 2 Michael Addition; 2.1 Chelating α,β-Unsaturated Compounds; 2.1.1 Chelating Compounds; 2.1.1.1 Alkylidene Malonates; 2.1.1.2 β,γ-Unsaturated α-Ketoesters; 2.1.1.3 α' -Hydroxy Enones
2.1.1.4 α' -Phosphonate Enones2.1.1.5 α,β-Unsaturated Acyl Compounds; 2.1.1.5.1 α,β-Unsaturated Acyl Phosphonates; 2.1.1.5.2 α,β-Unsaturated 2-Acyl Imidazoles; 2.1.1.6 α,β-Unsaturated Thioesters; 2.1.1.7 Nitroacrylates; 2.1.1.8 Experimental: Selected Procedures; 2.2 Simple α,β-Unsaturated Substrates; 2.2.1 Introduction; 2.2.1.1 α,β-Unsaturated Aldehydes; 2.2.1.1.1 Organocatalysis; 2.2.1.1.2 Organocatalytic Domino Reactions; 2.2.1.1.3 Experimental: Selected Procedures; 2.2.1.2 α,β-Unsaturated Ketones; 2.2.1.2.1 Organometallic Catalysis; 2.2.1.2.2 Organocatalysis 2.2.1.2.3 Experimental: Selected Procedures2.2.2 Intramolecular Approach; 2.3 Nitroalkenes; 2.3.1 Introduction; 2.3.2 Organocatalytic Enantioselective Reactions; 2.3.2.1 Friedel-Crafts Alkylation of Indoles; 2.3.2.1.1 Thiourea Catalysts; 2.3.2.1.2 Bissulfonamide Catalysts; 2.3.2.1.3 Phosphoric Acid Catalysts; 2.3.2.1.4 Synthetic Applications; 2.3.3 Friedel-Crafts Reactions of Naphthols; 2.3.3.1 Thiourea Catalysts; 2.3.4 Addition of 1,2,3-Triazoles; 2.3.4.1 Cinchona Alkaloids Catalysts; 2.3.5 Conclusion and Outlook; 2.3.6 Experimental: Selected Procedures 2.3.7 Lewis Acid Catalyzed Enantioselective Reactions2.3.7.1 Friedel-Crafts Reactions of Indoles; 2.3.7.1.1 Zinc Catalysts; 2.3.7.1.2 Copper and Aluminum Catalysts; 2.3.7.2 Friedel-Crafts Reactions of Furans and Pyrroles; 2.3.7.2.1 Zinc Catalysts; 2.3.7.3 Conclusion and Outlook; 2.3.7.4 Experimental: Selected Procedures; References; 3 Addition to Carbonyl Compounds; 3.1 Aldehydes/Ketones; 3.1.1 Introduction; 3.1.2 Organometallic Catalysis; 3.1.2.1 Fundamental Examples and Mechanism; 3.1.2.1.1 Chiral Titanium (IV) Catalysis; 3.1.2.1.2 Chiral Bisoxazoline-Cu(II) Catalysis 3.1.2.2 Experiments: Selected Representative Procedures3.1.3 Organocatalysis; 3.1.3.1 Fundamental Examples and Mechanism; 3.1.3.2 Experiments: Selected Representative Procedures; 3.1.4 Heterogeneous Catalysis; 3.2 Imines; 3.2.1 Catalytic Asymmetric Friedel-Crafts Reaction of Imines; 3.2.1.1 Intermolecular Approach; 3.2.1.1.1 Organometallic Catalysis; 3.2.1.1.2 Organocatalysis; 3.2.1.2 Pictet-Spengler Reaction; 3.2.2 Selected Procedures; References; 4 Nucleophilic Allylic Alkylation and Hydroarylation of Allenes; 4.1 Introduction; 4.2 Allylic Alkylations; 4.2.1 Intermolecular Approach 4.2.1.1 Benzene-Like Compounds |
| Record Nr. | UNINA-9910143128703321 |
| Weinheim, : Wiley-VCH, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Catalytic asymmetric Friedel-Crafts alkylations [[electronic resource] /] / edited by Marco Bandini and Achille Umani-Ronchi ; with a foreword by George A. Olah
| Catalytic asymmetric Friedel-Crafts alkylations [[electronic resource] /] / edited by Marco Bandini and Achille Umani-Ronchi ; with a foreword by George A. Olah |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2009 |
| Descrizione fisica | 1 online resource (319 p.) |
| Disciplina | 547.21 |
| Altri autori (Persone) |
BandiniMarco
Umani-RonchiAchille |
| Soggetto topico |
Friedel-Crafts reaction
Chemistry, Organic |
| ISBN |
1-282-68346-2
9786612683466 3-527-62697-2 3-527-62698-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Catalytic Asymmetric Friedel-Crafts Alkylations; Foreword; Contents; Preface; List of Contributors; 1 General Aspects and Historical Background; 1.1 Introduction; 1.2 General Aspects and Historical Background; 1.3 Catalytic Enantioselective FC Reactions: An Introduction; 1.3.1 Alkylating Agents; 1.3.2 Privileged Catalysts; 1.3.3 Aromatic Compounds and Reaction Conditions; References; 2 Michael Addition; 2.1 Chelating α,β-Unsaturated Compounds; 2.1.1 Chelating Compounds; 2.1.1.1 Alkylidene Malonates; 2.1.1.2 β,γ-Unsaturated α-Ketoesters; 2.1.1.3 α' -Hydroxy Enones
2.1.1.4 α' -Phosphonate Enones2.1.1.5 α,β-Unsaturated Acyl Compounds; 2.1.1.5.1 α,β-Unsaturated Acyl Phosphonates; 2.1.1.5.2 α,β-Unsaturated 2-Acyl Imidazoles; 2.1.1.6 α,β-Unsaturated Thioesters; 2.1.1.7 Nitroacrylates; 2.1.1.8 Experimental: Selected Procedures; 2.2 Simple α,β-Unsaturated Substrates; 2.2.1 Introduction; 2.2.1.1 α,β-Unsaturated Aldehydes; 2.2.1.1.1 Organocatalysis; 2.2.1.1.2 Organocatalytic Domino Reactions; 2.2.1.1.3 Experimental: Selected Procedures; 2.2.1.2 α,β-Unsaturated Ketones; 2.2.1.2.1 Organometallic Catalysis; 2.2.1.2.2 Organocatalysis 2.2.1.2.3 Experimental: Selected Procedures2.2.2 Intramolecular Approach; 2.3 Nitroalkenes; 2.3.1 Introduction; 2.3.2 Organocatalytic Enantioselective Reactions; 2.3.2.1 Friedel-Crafts Alkylation of Indoles; 2.3.2.1.1 Thiourea Catalysts; 2.3.2.1.2 Bissulfonamide Catalysts; 2.3.2.1.3 Phosphoric Acid Catalysts; 2.3.2.1.4 Synthetic Applications; 2.3.3 Friedel-Crafts Reactions of Naphthols; 2.3.3.1 Thiourea Catalysts; 2.3.4 Addition of 1,2,3-Triazoles; 2.3.4.1 Cinchona Alkaloids Catalysts; 2.3.5 Conclusion and Outlook; 2.3.6 Experimental: Selected Procedures 2.3.7 Lewis Acid Catalyzed Enantioselective Reactions2.3.7.1 Friedel-Crafts Reactions of Indoles; 2.3.7.1.1 Zinc Catalysts; 2.3.7.1.2 Copper and Aluminum Catalysts; 2.3.7.2 Friedel-Crafts Reactions of Furans and Pyrroles; 2.3.7.2.1 Zinc Catalysts; 2.3.7.3 Conclusion and Outlook; 2.3.7.4 Experimental: Selected Procedures; References; 3 Addition to Carbonyl Compounds; 3.1 Aldehydes/Ketones; 3.1.1 Introduction; 3.1.2 Organometallic Catalysis; 3.1.2.1 Fundamental Examples and Mechanism; 3.1.2.1.1 Chiral Titanium (IV) Catalysis; 3.1.2.1.2 Chiral Bisoxazoline-Cu(II) Catalysis 3.1.2.2 Experiments: Selected Representative Procedures3.1.3 Organocatalysis; 3.1.3.1 Fundamental Examples and Mechanism; 3.1.3.2 Experiments: Selected Representative Procedures; 3.1.4 Heterogeneous Catalysis; 3.2 Imines; 3.2.1 Catalytic Asymmetric Friedel-Crafts Reaction of Imines; 3.2.1.1 Intermolecular Approach; 3.2.1.1.1 Organometallic Catalysis; 3.2.1.1.2 Organocatalysis; 3.2.1.2 Pictet-Spengler Reaction; 3.2.2 Selected Procedures; References; 4 Nucleophilic Allylic Alkylation and Hydroarylation of Allenes; 4.1 Introduction; 4.2 Allylic Alkylations; 4.2.1 Intermolecular Approach 4.2.1.1 Benzene-Like Compounds |
| Record Nr. | UNINA-9910830993603321 |
| Weinheim, : Wiley-VCH, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Catalytic asymmetric Friedel-Crafts alkylations / / edited by Marco Bandini and Achille Umani-Ronchi ; with a foreword by George A. Olah
| Catalytic asymmetric Friedel-Crafts alkylations / / edited by Marco Bandini and Achille Umani-Ronchi ; with a foreword by George A. Olah |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2009 |
| Descrizione fisica | 1 online resource (319 p.) |
| Disciplina | 547.21 |
| Altri autori (Persone) |
BandiniMarco
Umani-RonchiAchille |
| Soggetto topico |
Friedel-Crafts reaction
Chemistry, Organic |
| ISBN |
1-282-68346-2
9786612683466 3-527-62697-2 3-527-62698-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Catalytic Asymmetric Friedel-Crafts Alkylations; Foreword; Contents; Preface; List of Contributors; 1 General Aspects and Historical Background; 1.1 Introduction; 1.2 General Aspects and Historical Background; 1.3 Catalytic Enantioselective FC Reactions: An Introduction; 1.3.1 Alkylating Agents; 1.3.2 Privileged Catalysts; 1.3.3 Aromatic Compounds and Reaction Conditions; References; 2 Michael Addition; 2.1 Chelating α,β-Unsaturated Compounds; 2.1.1 Chelating Compounds; 2.1.1.1 Alkylidene Malonates; 2.1.1.2 β,γ-Unsaturated α-Ketoesters; 2.1.1.3 α' -Hydroxy Enones
2.1.1.4 α' -Phosphonate Enones2.1.1.5 α,β-Unsaturated Acyl Compounds; 2.1.1.5.1 α,β-Unsaturated Acyl Phosphonates; 2.1.1.5.2 α,β-Unsaturated 2-Acyl Imidazoles; 2.1.1.6 α,β-Unsaturated Thioesters; 2.1.1.7 Nitroacrylates; 2.1.1.8 Experimental: Selected Procedures; 2.2 Simple α,β-Unsaturated Substrates; 2.2.1 Introduction; 2.2.1.1 α,β-Unsaturated Aldehydes; 2.2.1.1.1 Organocatalysis; 2.2.1.1.2 Organocatalytic Domino Reactions; 2.2.1.1.3 Experimental: Selected Procedures; 2.2.1.2 α,β-Unsaturated Ketones; 2.2.1.2.1 Organometallic Catalysis; 2.2.1.2.2 Organocatalysis 2.2.1.2.3 Experimental: Selected Procedures2.2.2 Intramolecular Approach; 2.3 Nitroalkenes; 2.3.1 Introduction; 2.3.2 Organocatalytic Enantioselective Reactions; 2.3.2.1 Friedel-Crafts Alkylation of Indoles; 2.3.2.1.1 Thiourea Catalysts; 2.3.2.1.2 Bissulfonamide Catalysts; 2.3.2.1.3 Phosphoric Acid Catalysts; 2.3.2.1.4 Synthetic Applications; 2.3.3 Friedel-Crafts Reactions of Naphthols; 2.3.3.1 Thiourea Catalysts; 2.3.4 Addition of 1,2,3-Triazoles; 2.3.4.1 Cinchona Alkaloids Catalysts; 2.3.5 Conclusion and Outlook; 2.3.6 Experimental: Selected Procedures 2.3.7 Lewis Acid Catalyzed Enantioselective Reactions2.3.7.1 Friedel-Crafts Reactions of Indoles; 2.3.7.1.1 Zinc Catalysts; 2.3.7.1.2 Copper and Aluminum Catalysts; 2.3.7.2 Friedel-Crafts Reactions of Furans and Pyrroles; 2.3.7.2.1 Zinc Catalysts; 2.3.7.3 Conclusion and Outlook; 2.3.7.4 Experimental: Selected Procedures; References; 3 Addition to Carbonyl Compounds; 3.1 Aldehydes/Ketones; 3.1.1 Introduction; 3.1.2 Organometallic Catalysis; 3.1.2.1 Fundamental Examples and Mechanism; 3.1.2.1.1 Chiral Titanium (IV) Catalysis; 3.1.2.1.2 Chiral Bisoxazoline-Cu(II) Catalysis 3.1.2.2 Experiments: Selected Representative Procedures3.1.3 Organocatalysis; 3.1.3.1 Fundamental Examples and Mechanism; 3.1.3.2 Experiments: Selected Representative Procedures; 3.1.4 Heterogeneous Catalysis; 3.2 Imines; 3.2.1 Catalytic Asymmetric Friedel-Crafts Reaction of Imines; 3.2.1.1 Intermolecular Approach; 3.2.1.1.1 Organometallic Catalysis; 3.2.1.1.2 Organocatalysis; 3.2.1.2 Pictet-Spengler Reaction; 3.2.2 Selected Procedures; References; 4 Nucleophilic Allylic Alkylation and Hydroarylation of Allenes; 4.1 Introduction; 4.2 Allylic Alkylations; 4.2.1 Intermolecular Approach 4.2.1.1 Benzene-Like Compounds |
| Record Nr. | UNINA-9910877619503321 |
| Weinheim, : Wiley-VCH, c2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||