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Amines grafted cellulose materials [[electronic resource] /] / Nadege Follain
| Amines grafted cellulose materials [[electronic resource] /] / Nadege Follain |
| Autore | Follain Nadege |
| Pubbl/distr/stampa | New York, : Nova Science Publishers, c2010 |
| Descrizione fisica | 1 online resource (78 p.) |
| Collana |
Materials science and technologies
Novinka |
| Soggetto topico |
Cellulose - Oxidation
Amines |
| Soggetto genere / forma | Electronic books. |
| ISBN | 1-61668-494-1 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910452983803321 |
Follain Nadege
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| New York, : Nova Science Publishers, c2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Amines grafted cellulose materials [[electronic resource] /] / Nadege Follain
| Amines grafted cellulose materials [[electronic resource] /] / Nadege Follain |
| Autore | Follain Nadege |
| Pubbl/distr/stampa | New York, : Nova Science Publishers, c2010 |
| Descrizione fisica | 1 online resource (78 p.) |
| Collana |
Materials science and technologies
Novinka |
| Soggetto topico |
Cellulose - Oxidation
Amines |
| ISBN | 1-61668-494-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910779503703321 |
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Follain Nadege
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| New York, : Nova Science Publishers, c2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Amines grafted cellulose materials [[electronic resource] /] / Nadege Follain
| Amines grafted cellulose materials [[electronic resource] /] / Nadege Follain |
| Autore | Follain Nadege |
| Pubbl/distr/stampa | New York, : Nova Science Publishers, c2010 |
| Descrizione fisica | 1 online resource (78 p.) |
| Collana |
Materials science and technologies
Novinka |
| Soggetto topico |
Cellulose - Oxidation
Amines |
| ISBN | 1-61668-494-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910816363103321 |
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Follain Nadege
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| New York, : Nova Science Publishers, c2010 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Catecholamines : physiology, pharmacology, and pathology for students and clinicians / / Lewis Landsberg, MD, Irving S. Cutter Professor of Medicine, Dean Emeritus, Director, Northwestern Comprehensive Center on Obesity (NCCO), Northwestern University Feinberg School of Medicine, Chicago, Illinois
| Catecholamines : physiology, pharmacology, and pathology for students and clinicians / / Lewis Landsberg, MD, Irving S. Cutter Professor of Medicine, Dean Emeritus, Director, Northwestern Comprehensive Center on Obesity (NCCO), Northwestern University Feinberg School of Medicine, Chicago, Illinois |
| Autore | Landsberg Lewis <1938-> |
| Pubbl/distr/stampa | Philadelphia : , : Wolters Kluwer, , [2017] |
| Descrizione fisica | 1 online resource (159 pages) : illustrations |
| Disciplina | 612.8/042 |
| Soggetto topico |
Catecholamines
Amines Hormones Biochemistry |
| Soggetto genere / forma | Electronic books. |
| ISBN | 1-4963-7532-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910478865803321 |
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Landsberg Lewis <1938->
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| Philadelphia : , : Wolters Kluwer, , [2017] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Catecholamines : physiology, pharmacology, and pathology for students and clinicians / / Lewis Landsberg, MD, Irving S. Cutter Professor of Medicine, Dean Emeritus, Director, Northwestern Comprehensive Center on Obesity (NCCO), Northwestern University Feinberg School of Medicine, Chicago, Illinois
| Catecholamines : physiology, pharmacology, and pathology for students and clinicians / / Lewis Landsberg, MD, Irving S. Cutter Professor of Medicine, Dean Emeritus, Director, Northwestern Comprehensive Center on Obesity (NCCO), Northwestern University Feinberg School of Medicine, Chicago, Illinois |
| Autore | Landsberg Lewis <1938-> |
| Pubbl/distr/stampa | Philadelphia : , : Wolters Kluwer, , [2017] |
| Descrizione fisica | 1 online resource (159 pages) : illustrations |
| Disciplina | 612.8/042 |
| Soggetto topico |
Catecholamines
Amines Hormones Biochemistry |
| ISBN | 1-4963-7532-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910796045703321 |
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Landsberg Lewis <1938->
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| Philadelphia : , : Wolters Kluwer, , [2017] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Catecholamines : physiology, pharmacology, and pathology for students and clinicians / / Lewis Landsberg, MD, Irving S. Cutter Professor of Medicine, Dean Emeritus, Director, Northwestern Comprehensive Center on Obesity (NCCO), Northwestern University Feinberg School of Medicine, Chicago, Illinois
| Catecholamines : physiology, pharmacology, and pathology for students and clinicians / / Lewis Landsberg, MD, Irving S. Cutter Professor of Medicine, Dean Emeritus, Director, Northwestern Comprehensive Center on Obesity (NCCO), Northwestern University Feinberg School of Medicine, Chicago, Illinois |
| Autore | Landsberg Lewis <1938-> |
| Pubbl/distr/stampa | Philadelphia : , : Wolters Kluwer, , [2017] |
| Descrizione fisica | 1 online resource (159 pages) : illustrations |
| Disciplina | 612.8/042 |
| Soggetto topico |
Catecholamines
Amines Hormones Biochemistry |
| ISBN | 1-4963-7532-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910828703503321 |
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Landsberg Lewis <1938->
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| Philadelphia : , : Wolters Kluwer, , [2017] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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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 | ||
| ||
Modern amination methods [[electronic resource] /] / edited by Alfredo Ricci
| Modern amination methods [[electronic resource] /] / edited by Alfredo Ricci |
| Pubbl/distr/stampa | Weinheim ; ; Cambridge, : Wiley-VCH, c2000 |
| Descrizione fisica | 1 online resource (288 p.) |
| Disciplina |
547.25
660 |
| Altri autori (Persone) | RicciAlfredo <1939-> |
| Soggetto topico |
Amination - Methodology
Amines |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-281-76409-4
9786611764098 3-527-61318-8 3-527-61319-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Modern Amination Methods; Preface; Contents; List of Authors; Chapter 1 Modem Allylic Amination Methods; 1.1 Introduction; 1.2 Nucleophilic Amination of Functionalized Alkenes; 1.2.1 Amination of Allyl Alcohols; 1.2.2 Amination of Allyl halides; 1.2.2.1 Amination of Allyl Halides and Acetates Catalyzed by metal Complexes; 1.2.3 Electrophilic Amination of Non-Functionalized Alkenes; 1.2.4 Amination with Nitrene Complexes; 1.2.5 Amination Based on Ene-Reaction-Like Processes; 1.2.5.1 Type 1 Reactions: Ene Reaction Followed by [2,3]-Sigmatropic Rearrangement; 1.2.5.2 Type 2 Ene Reactions
1.2.6 Allylic Amination with Ar-NX and a Metal Catalyst1.3 Summary; Acknowledgments; References; Chapter 2 Eletrophilic Amination Routes from Alkenes; 2.1 Introduction; 2.2 Indirect Stoichiometric Amination; 2.2.1 Amination via Organoboron Compounds; 2.2.1.1 Applications to the Synthesis of Primary Amines; 2.2.1.2 Applications to the Synthesis of Secondary Amines; 2.2.1.3 Applications to the Synthesis of Tertiary Amines; 2.2.2 Amination via Organozirconium Compounds; 2.3 Indirect Catalytic Amination; 2.4 Direct Alkene Amination; References Chapter 3 Stereoselective Electrophilic Amination with Sulfonyloxycarbamates and Azodicarboxylates3.1 Introduction; 3.2 Sulfonyloxycarbamates; 3.2.1 Preparation of N-[(arylsulfonyl)oxy]carbamates; 3.2.2 Stereoselective Synthesis of a-Amino Carboxylic and Phosphonic Acids via Electrophilic Amination with Lithium rerr-Butyl N-(tosyloxy) Carbamate; 3.2.2.1 α-Amino Carboxylic Acids; 3.2.2.2 α-Amino Phosphonic Acids; 3.2.3 Reactions of Ethyl N-((p-nitrobenzenesulfonyl)oxy(carbamate with Chiral Enamines and Enol Ethers; 3.3 Dialkylazodicarboxylates 3.3.1 Electrophilic Amination of Silyl Ketene Acetals3.3.2 Electrophilic Amination of Chiral Amide Enolates; 3.3.3 Electrophilic Amination of Chiral Ester Enolates; 3.3.3.1 β-Hydroxy Esters; 3.3.3.2 β-Amino Esters; 3.3.4 Electrophilic Amination of Ketone Enolates; 3.3.5 Electrophilic Amination of Phosphorous-Stabilized Anions; 3.3.5.1 Oxazaphospholanes; 3.3.5.2 Diazaphospholidines; 3.4 Chiral Electrophilic Aminating Reagents; 3.4.1 Azodicarboxylates and Azodicarboxamides; 3.4.2 Chiral Catalytic Approach; 3.5 Conclusion; References Chapter 4 Glycosylamines as Auxiliaries in Stereoselective Syntheses of Chiral Amino Compounds4.1 Introduction; 4.1.1 Exo Anomeric Effect; 4.1.2 Influence of Coordinating Centers; 4.1.3 Pseudo-Enantiomeric Carbohydrates in Stereoselective Syntheses; 4.2 Syntheses of Amino Acids; 4.2.1 Syntheses of Enantiomerically Pure a-Amino Acids; 4.2.2 Syntheses of Enantiomerically Pure β-Amino Acids; 4.2.3 Rearrangement Reactions; 4.2.4 Stereoselective Multicomponent Reactions; 4.3 Stereoselective Syntheses of Chiral Heterocycles; 4.3.1 Heterocycles Through Cycloaddition Reactions 4.3.2 Stereoselective Syntheses of Chiral Piperidines via Addition Reactions to 4-Pyridones |
| Record Nr. | UNINA-9910144283403321 |
| Weinheim ; ; Cambridge, : Wiley-VCH, c2000 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Modern amination methods [[electronic resource] /] / edited by Alfredo Ricci
| Modern amination methods [[electronic resource] /] / edited by Alfredo Ricci |
| Pubbl/distr/stampa | Weinheim ; ; Cambridge, : Wiley-VCH, c2000 |
| Descrizione fisica | 1 online resource (288 p.) |
| Disciplina |
547.25
660 |
| Altri autori (Persone) | RicciAlfredo <1939-> |
| Soggetto topico |
Amination - Methodology
Amines |
| ISBN |
1-281-76409-4
9786611764098 3-527-61318-8 3-527-61319-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Modern Amination Methods; Preface; Contents; List of Authors; Chapter 1 Modem Allylic Amination Methods; 1.1 Introduction; 1.2 Nucleophilic Amination of Functionalized Alkenes; 1.2.1 Amination of Allyl Alcohols; 1.2.2 Amination of Allyl halides; 1.2.2.1 Amination of Allyl Halides and Acetates Catalyzed by metal Complexes; 1.2.3 Electrophilic Amination of Non-Functionalized Alkenes; 1.2.4 Amination with Nitrene Complexes; 1.2.5 Amination Based on Ene-Reaction-Like Processes; 1.2.5.1 Type 1 Reactions: Ene Reaction Followed by [2,3]-Sigmatropic Rearrangement; 1.2.5.2 Type 2 Ene Reactions
1.2.6 Allylic Amination with Ar-NX and a Metal Catalyst1.3 Summary; Acknowledgments; References; Chapter 2 Eletrophilic Amination Routes from Alkenes; 2.1 Introduction; 2.2 Indirect Stoichiometric Amination; 2.2.1 Amination via Organoboron Compounds; 2.2.1.1 Applications to the Synthesis of Primary Amines; 2.2.1.2 Applications to the Synthesis of Secondary Amines; 2.2.1.3 Applications to the Synthesis of Tertiary Amines; 2.2.2 Amination via Organozirconium Compounds; 2.3 Indirect Catalytic Amination; 2.4 Direct Alkene Amination; References Chapter 3 Stereoselective Electrophilic Amination with Sulfonyloxycarbamates and Azodicarboxylates3.1 Introduction; 3.2 Sulfonyloxycarbamates; 3.2.1 Preparation of N-[(arylsulfonyl)oxy]carbamates; 3.2.2 Stereoselective Synthesis of a-Amino Carboxylic and Phosphonic Acids via Electrophilic Amination with Lithium rerr-Butyl N-(tosyloxy) Carbamate; 3.2.2.1 α-Amino Carboxylic Acids; 3.2.2.2 α-Amino Phosphonic Acids; 3.2.3 Reactions of Ethyl N-((p-nitrobenzenesulfonyl)oxy(carbamate with Chiral Enamines and Enol Ethers; 3.3 Dialkylazodicarboxylates 3.3.1 Electrophilic Amination of Silyl Ketene Acetals3.3.2 Electrophilic Amination of Chiral Amide Enolates; 3.3.3 Electrophilic Amination of Chiral Ester Enolates; 3.3.3.1 β-Hydroxy Esters; 3.3.3.2 β-Amino Esters; 3.3.4 Electrophilic Amination of Ketone Enolates; 3.3.5 Electrophilic Amination of Phosphorous-Stabilized Anions; 3.3.5.1 Oxazaphospholanes; 3.3.5.2 Diazaphospholidines; 3.4 Chiral Electrophilic Aminating Reagents; 3.4.1 Azodicarboxylates and Azodicarboxamides; 3.4.2 Chiral Catalytic Approach; 3.5 Conclusion; References Chapter 4 Glycosylamines as Auxiliaries in Stereoselective Syntheses of Chiral Amino Compounds4.1 Introduction; 4.1.1 Exo Anomeric Effect; 4.1.2 Influence of Coordinating Centers; 4.1.3 Pseudo-Enantiomeric Carbohydrates in Stereoselective Syntheses; 4.2 Syntheses of Amino Acids; 4.2.1 Syntheses of Enantiomerically Pure a-Amino Acids; 4.2.2 Syntheses of Enantiomerically Pure β-Amino Acids; 4.2.3 Rearrangement Reactions; 4.2.4 Stereoselective Multicomponent Reactions; 4.3 Stereoselective Syntheses of Chiral Heterocycles; 4.3.1 Heterocycles Through Cycloaddition Reactions 4.3.2 Stereoselective Syntheses of Chiral Piperidines via Addition Reactions to 4-Pyridones |
| Record Nr. | UNINA-9910830632103321 |
| Weinheim ; ; Cambridge, : Wiley-VCH, c2000 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Soggetto topico
-
Amines
(13)
- Catecholamines (5)
- Biochemistry (3)
- Cellulose - Oxidation (3)
- Hormones (3)