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Chiral amine synthesis [[electronic resource] ] : methods, developments and applications / / edited by Thomas C. Nugent
| Chiral amine synthesis [[electronic resource] ] : methods, developments and applications / / edited by Thomas C. Nugent |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 |
| Descrizione fisica | 1 online resource (522 p.) |
| Disciplina | 547.042 |
| Soggetto topico |
Chirality
Amines |
| ISBN |
1-282-46293-8
9786612462931 3-527-62954-8 3-527-62955-6 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Chiral Amine Synthesis; Foreword; Contents; Preface; List of Contributors; 1 Stereoselective Synthesis of a-Branched Amines by Nucleophilic Addition of Unstabilized Carbanions to Imines; 1.1 Introduction; 1.2 Overview of the Methods for the Preparation of Imines; 1.2.1 N-Aryl and N-Alkyl Imines and Hydrazones; 1.2.2 N-Sulfinyl Imines; 1.2.3 N-Sulfonyl Imines; 1.2.4 N-Phosphinoyl Imines; 1.2.5 N-Acyl and N-Carbamoyl Imines; 1.3 Chiral Auxiliary-Based Approaches; 1.3.1 Imines Derived from Chiral Aldehydes; 1.3.2 Imines Bearing a Chiral Protecting/Activating Group
1.4 Catalytic Asymmetric Nucleophilic Addition to Achiral Imines1.4.1 Catalytic Asymmetric Addition of sp3 Hybridized Carbanions; 1.4.1.1 Copper-Catalyzed Dialkylzinc Additions; 1.4.1.2 Zinc Alkoxide-Catalyzed Dialkylzinc Additions; 1.4.1.3 Early Transition Metal (Zr, Hf)-Catalyzed Dialkylzinc Additions; 1.4.1.4 Rhodium-Catalyzed Dialkylzinc Addition Reactions; 1.4.2 Catalytic Asymmetric Allylation of Imines; 1.4.3 Catalytic Asymmetric Addition of sp2 Hybridized Carbanions; 1.4.3.1 Catalytic Asymmetric Vinylation; 1.4.3.2 Catalytic Asymmetric Arylation 1.4.3.2.1 Amino Alcohol-Catalyzed Addition of Organozinc Reagents1.4.3.2.2 Rhodium Phosphine-Catalyzed Arylation of Imines; 1.4.3.2.3 Rhodium Diene-Catalyzed Arylation of Imines; 1.4.4 Catalytic Asymmetric Addition of sp Hybridized Carbanions; 1.5 Conclusion; References; 2 Asymmetric Methods for Radical Addition to Imino Compounds; 2.1 Background and Introduction; 2.2 Intermolecular Radical Addition Chiral N-Acylhydrazones; 2.2.1 Design of Chiral N-Acylhydrazones; 2.2.2 Preparation of Chiral N-Acylhydrazones; 2.2.3 Tin-Mediated Addition of Secondary and Tertiary Radicals 2.2.4 Tin-Free Radical Addition2.2.5 Manganese-Mediated Radical Addition; 2.2.6 Manganese-Mediated Coupling with Multifunctional Precursors; 2.2.6.1 Hybrid Radical-Ionic Annulation; 2.2.6.2 Precursors Containing Hydroxyl or Protected Hydroxyl Groups; 2.2.6.3 Ester-Containing N-Acylhydrazones; 2.2.6.4 Additions to Ketone Hydrazones; 2.3 Asymmetric Catalysis of Radical Addition; 2.4 Closing Remarks; References; 3 Enantioselective Synthesis of Amines by Chiral Brønsted Acid Catalysts; 3.1 Introduction; 3.2 Carbon-Carbon Bond Forming Reactions; 3.2.1 Mannich and Related Reactions 3.2.1.1 Mannich Reaction3.2.1.2 Nucleophilic Addition of Diazoacetates to Aldimine; 3.2.1.3 Vinylogous Mannich Reaction; 3.2.1.4 Aza-Petasis-Ferrier Rearrangement; 3.2.2 One-Carbon Homologation Reactions; 3.2.2.1 Strecker Reaction; 3.2.2.2 Aza-Henry Reaction; 3.2.2.3 Imino-Azaenamine Reaction; 3.2.3 Friedel-Crafts and Related Reactions; 3.2.3.1 Friedel-Crafts Reaction via Activation of Aldimines; 3.2.3.2 Friedel-Crafts Reaction via Activation of Electron-Rich Alkenes; 3.2.3.3 Pictet-Spengler Reaction; 3.2.4 Cycloaddition Reactions 3.2.4.1 Hetero-Diels-Alder Reaction of Aldimines with Siloxydienes |
| Record Nr. | UNINA-9910139470603321 |
| Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chiral amine synthesis [[electronic resource] ] : methods, developments and applications / / edited by Thomas C. Nugent
| Chiral amine synthesis [[electronic resource] ] : methods, developments and applications / / edited by Thomas C. Nugent |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 |
| Descrizione fisica | 1 online resource (522 p.) |
| Disciplina | 547.042 |
| Soggetto topico |
Chirality
Amines |
| Soggetto genere / forma |
Handbook
handbooks. Reference works Handbooks and manuals Handbooks and manuals. Reference works. Guides et manuels. Ouvrages de référence |
| ISBN |
1-282-46293-8
9786612462931 3-527-62954-8 3-527-62955-6 |
| Classificazione | 540 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Chiral Amine Synthesis; Foreword; Contents; Preface; List of Contributors; 1 Stereoselective Synthesis of a-Branched Amines by Nucleophilic Addition of Unstabilized Carbanions to Imines; 1.1 Introduction; 1.2 Overview of the Methods for the Preparation of Imines; 1.2.1 N-Aryl and N-Alkyl Imines and Hydrazones; 1.2.2 N-Sulfinyl Imines; 1.2.3 N-Sulfonyl Imines; 1.2.4 N-Phosphinoyl Imines; 1.2.5 N-Acyl and N-Carbamoyl Imines; 1.3 Chiral Auxiliary-Based Approaches; 1.3.1 Imines Derived from Chiral Aldehydes; 1.3.2 Imines Bearing a Chiral Protecting/Activating Group
1.4 Catalytic Asymmetric Nucleophilic Addition to Achiral Imines1.4.1 Catalytic Asymmetric Addition of sp3 Hybridized Carbanions; 1.4.1.1 Copper-Catalyzed Dialkylzinc Additions; 1.4.1.2 Zinc Alkoxide-Catalyzed Dialkylzinc Additions; 1.4.1.3 Early Transition Metal (Zr, Hf)-Catalyzed Dialkylzinc Additions; 1.4.1.4 Rhodium-Catalyzed Dialkylzinc Addition Reactions; 1.4.2 Catalytic Asymmetric Allylation of Imines; 1.4.3 Catalytic Asymmetric Addition of sp2 Hybridized Carbanions; 1.4.3.1 Catalytic Asymmetric Vinylation; 1.4.3.2 Catalytic Asymmetric Arylation 1.4.3.2.1 Amino Alcohol-Catalyzed Addition of Organozinc Reagents1.4.3.2.2 Rhodium Phosphine-Catalyzed Arylation of Imines; 1.4.3.2.3 Rhodium Diene-Catalyzed Arylation of Imines; 1.4.4 Catalytic Asymmetric Addition of sp Hybridized Carbanions; 1.5 Conclusion; References; 2 Asymmetric Methods for Radical Addition to Imino Compounds; 2.1 Background and Introduction; 2.2 Intermolecular Radical Addition Chiral N-Acylhydrazones; 2.2.1 Design of Chiral N-Acylhydrazones; 2.2.2 Preparation of Chiral N-Acylhydrazones; 2.2.3 Tin-Mediated Addition of Secondary and Tertiary Radicals 2.2.4 Tin-Free Radical Addition2.2.5 Manganese-Mediated Radical Addition; 2.2.6 Manganese-Mediated Coupling with Multifunctional Precursors; 2.2.6.1 Hybrid Radical-Ionic Annulation; 2.2.6.2 Precursors Containing Hydroxyl or Protected Hydroxyl Groups; 2.2.6.3 Ester-Containing N-Acylhydrazones; 2.2.6.4 Additions to Ketone Hydrazones; 2.3 Asymmetric Catalysis of Radical Addition; 2.4 Closing Remarks; References; 3 Enantioselective Synthesis of Amines by Chiral Brønsted Acid Catalysts; 3.1 Introduction; 3.2 Carbon-Carbon Bond Forming Reactions; 3.2.1 Mannich and Related Reactions 3.2.1.1 Mannich Reaction3.2.1.2 Nucleophilic Addition of Diazoacetates to Aldimine; 3.2.1.3 Vinylogous Mannich Reaction; 3.2.1.4 Aza-Petasis-Ferrier Rearrangement; 3.2.2 One-Carbon Homologation Reactions; 3.2.2.1 Strecker Reaction; 3.2.2.2 Aza-Henry Reaction; 3.2.2.3 Imino-Azaenamine Reaction; 3.2.3 Friedel-Crafts and Related Reactions; 3.2.3.1 Friedel-Crafts Reaction via Activation of Aldimines; 3.2.3.2 Friedel-Crafts Reaction via Activation of Electron-Rich Alkenes; 3.2.3.3 Pictet-Spengler Reaction; 3.2.4 Cycloaddition Reactions 3.2.4.1 Hetero-Diels-Alder Reaction of Aldimines with Siloxydienes |
| Record Nr. | UNINA-9910829885503321 |
| Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chiral amine synthesis [[electronic resource] ] : methods, developments and applications / / edited by Thomas C. Nugent
| Chiral amine synthesis [[electronic resource] ] : methods, developments and applications / / edited by Thomas C. Nugent |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 |
| Descrizione fisica | 1 online resource (522 p.) |
| Disciplina | 547.042 |
| Soggetto topico |
Chirality
Amines |
| Soggetto genere / forma |
Handbook
handbooks. Reference works Handbooks and manuals Handbooks and manuals. Reference works. Guides et manuels. Ouvrages de référence |
| ISBN |
1-282-46293-8
9786612462931 3-527-62954-8 3-527-62955-6 |
| Classificazione | 540 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Chiral Amine Synthesis; Foreword; Contents; Preface; List of Contributors; 1 Stereoselective Synthesis of a-Branched Amines by Nucleophilic Addition of Unstabilized Carbanions to Imines; 1.1 Introduction; 1.2 Overview of the Methods for the Preparation of Imines; 1.2.1 N-Aryl and N-Alkyl Imines and Hydrazones; 1.2.2 N-Sulfinyl Imines; 1.2.3 N-Sulfonyl Imines; 1.2.4 N-Phosphinoyl Imines; 1.2.5 N-Acyl and N-Carbamoyl Imines; 1.3 Chiral Auxiliary-Based Approaches; 1.3.1 Imines Derived from Chiral Aldehydes; 1.3.2 Imines Bearing a Chiral Protecting/Activating Group
1.4 Catalytic Asymmetric Nucleophilic Addition to Achiral Imines1.4.1 Catalytic Asymmetric Addition of sp3 Hybridized Carbanions; 1.4.1.1 Copper-Catalyzed Dialkylzinc Additions; 1.4.1.2 Zinc Alkoxide-Catalyzed Dialkylzinc Additions; 1.4.1.3 Early Transition Metal (Zr, Hf)-Catalyzed Dialkylzinc Additions; 1.4.1.4 Rhodium-Catalyzed Dialkylzinc Addition Reactions; 1.4.2 Catalytic Asymmetric Allylation of Imines; 1.4.3 Catalytic Asymmetric Addition of sp2 Hybridized Carbanions; 1.4.3.1 Catalytic Asymmetric Vinylation; 1.4.3.2 Catalytic Asymmetric Arylation 1.4.3.2.1 Amino Alcohol-Catalyzed Addition of Organozinc Reagents1.4.3.2.2 Rhodium Phosphine-Catalyzed Arylation of Imines; 1.4.3.2.3 Rhodium Diene-Catalyzed Arylation of Imines; 1.4.4 Catalytic Asymmetric Addition of sp Hybridized Carbanions; 1.5 Conclusion; References; 2 Asymmetric Methods for Radical Addition to Imino Compounds; 2.1 Background and Introduction; 2.2 Intermolecular Radical Addition Chiral N-Acylhydrazones; 2.2.1 Design of Chiral N-Acylhydrazones; 2.2.2 Preparation of Chiral N-Acylhydrazones; 2.2.3 Tin-Mediated Addition of Secondary and Tertiary Radicals 2.2.4 Tin-Free Radical Addition2.2.5 Manganese-Mediated Radical Addition; 2.2.6 Manganese-Mediated Coupling with Multifunctional Precursors; 2.2.6.1 Hybrid Radical-Ionic Annulation; 2.2.6.2 Precursors Containing Hydroxyl or Protected Hydroxyl Groups; 2.2.6.3 Ester-Containing N-Acylhydrazones; 2.2.6.4 Additions to Ketone Hydrazones; 2.3 Asymmetric Catalysis of Radical Addition; 2.4 Closing Remarks; References; 3 Enantioselective Synthesis of Amines by Chiral Brønsted Acid Catalysts; 3.1 Introduction; 3.2 Carbon-Carbon Bond Forming Reactions; 3.2.1 Mannich and Related Reactions 3.2.1.1 Mannich Reaction3.2.1.2 Nucleophilic Addition of Diazoacetates to Aldimine; 3.2.1.3 Vinylogous Mannich Reaction; 3.2.1.4 Aza-Petasis-Ferrier Rearrangement; 3.2.2 One-Carbon Homologation Reactions; 3.2.2.1 Strecker Reaction; 3.2.2.2 Aza-Henry Reaction; 3.2.2.3 Imino-Azaenamine Reaction; 3.2.3 Friedel-Crafts and Related Reactions; 3.2.3.1 Friedel-Crafts Reaction via Activation of Aldimines; 3.2.3.2 Friedel-Crafts Reaction via Activation of Electron-Rich Alkenes; 3.2.3.3 Pictet-Spengler Reaction; 3.2.4 Cycloaddition Reactions 3.2.4.1 Hetero-Diels-Alder Reaction of Aldimines with Siloxydienes |
| Record Nr. | UNINA-9910840672703321 |
| Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||