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Biblioteca

MARC Lista (tabellare)
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  
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
Follain Nadege  
New York, : Nova Science Publishers, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Amines grafted cellulose materials / / Nadege Follain
Amines grafted cellulose materials / / Nadege Follain
Autore Follain Nadege
Edizione [1st ed.]
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-9910972863603321
Follain Nadege  
New York, : Nova Science Publishers, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Analysis of biogenic amines and their related enzymes / / edited by David Glick
Analysis of biogenic amines and their related enzymes / / edited by David Glick
Edizione [1st ed.]
Pubbl/distr/stampa New York, : Interscience, 1971
Descrizione fisica 1 online resource (360 pages)
Disciplina 544.94
574.192
Altri autori (Persone) GlickDavid <1908->
Collana Methods of biochemical analysis
Soggetto topico Amines
Biochemistry
ISBN 9786612313127
9781282313125
1282313126
9780470110409
0470110406
9780470110829
0470110821
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto METHODS OF BIOCHEMICAL ANALYSIS; CONTENTS; Assay of Serotonin. Related Metabolites. and Enzymes; Determination of Amine Oxidases; The Chemical Determination of Histamine; Determination of Histidine Decarboxylase Activity; The Chemical Estimation of Catecholamines and Their Metabolites in Body Fluids and Tissue Extracts; Assay of Enzymes of Catecholamine Biosynthesis and Metabolism; Measurement of Choline Esters; Determination of Activity of Cholinesterases; Measurement of Choline Acetylase; Author Index; Subject Index; Cumulative Index, Volumes 1-19 and Supplement
Record Nr. UNINA-9910819169003321
New York, : Interscience, 1971
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
Landsberg Lewis <1938->  
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
Landsberg Lewis <1938->  
Philadelphia : , : Wolters Kluwer, , [2017]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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
Landsberg Lewis <1938->  
Philadelphia : , : Wolters Kluwer, , [2017]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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
Opac: Controlla la disponibilità qui
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
Opac: Controlla la disponibilità qui
Chiral amine synthesis : methods, developments and applications / / edited by Thomas C. Nugent
Chiral amine synthesis : 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.
Guides et manuels.
Ouvrages de référence
ISBN 9786612462931
9781282462939
1282462938
9783527629541
3527629548
9783527629558
3527629556
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-9911018786103321
Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui