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Amino Acids, Peptides and Proteins [[electronic resource]] . Volume 33
| Amino Acids, Peptides and Proteins [[electronic resource]] . Volume 33 |
| Autore | Barrett G. C |
| Pubbl/distr/stampa | Cambridge, : Royal Society of Chemistry, 2002 |
| Descrizione fisica | 1 online resource (467 p.) |
| Disciplina |
547.042
547.75 547/.0/42 |
| Altri autori (Persone) |
DaviesJ. S. <1940->
ElmoreDonald Trevor |
| Collana | Specialist Periodical Reports |
| Soggetto topico |
Amino acids -- Periodicals
Peptides -- Periodicals Proteins -- Periodicals Biochemistry Chemistry Physical Sciences & Mathematics |
| Soggetto genere / forma | Electronic books. |
| ISBN | 1-84755-743-0 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | AM9780854042371-FX001; 9780854042371txt |
| Record Nr. | UNINA-9910449792203321 |
Barrett G. C
|
||
| Cambridge, : Royal Society of Chemistry, 2002 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Amino Acids, Peptides and Proteins [[electronic resource]] . Volume 33
| Amino Acids, Peptides and Proteins [[electronic resource]] . Volume 33 |
| Autore | Barrett G. C |
| Pubbl/distr/stampa | Cambridge, : Royal Society of Chemistry, 2002 |
| Descrizione fisica | 1 online resource (467 p.) |
| Disciplina |
547.042
547.75 547/.0/42 |
| Altri autori (Persone) |
DaviesJ. S. <1940->
ElmoreDonald Trevor |
| Collana | Specialist Periodical Reports |
| Soggetto topico |
Amino acids -- Periodicals
Peptides -- Periodicals Proteins -- Periodicals Biochemistry Chemistry Physical Sciences & Mathematics |
| ISBN | 1-84755-743-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | AM9780854042371-FX001; 9780854042371txt |
| Record Nr. | UNINA-9910777348703321 |
|
Barrett G. C
|
||
| Cambridge, : Royal Society of Chemistry, 2002 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Amino Acids, Peptides and Proteins . Volume 33
| Amino Acids, Peptides and Proteins . Volume 33 |
| Autore | Barrett G. C |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Cambridge, : Royal Society of Chemistry, 2002 |
| Descrizione fisica | 1 online resource (467 p.) |
| Disciplina |
547.042
547.75 547/.0/42 |
| Altri autori (Persone) |
DaviesJ. S. <1940->
ElmoreDonald Trevor |
| Collana | Specialist Periodical Reports |
| Soggetto topico |
Amino acids -- Periodicals
Peptides -- Periodicals Proteins -- Periodicals Biochemistry Chemistry Physical Sciences & Mathematics |
| ISBN | 1-84755-743-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | AM9780854042371-FX001; 9780854042371txt |
| Record Nr. | UNINA-9910828401303321 |
|
Barrett G. C
|
||
| Cambridge, : Royal Society of Chemistry, 2002 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Amino group chemistry : from synthesis to the life sciences / / edited by Alfredo Ricci
| Amino group chemistry : from synthesis to the life sciences / / edited by Alfredo Ricci |
| Pubbl/distr/stampa | Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008 |
| Descrizione fisica | 1 online resource (410 p.) |
| Disciplina |
547.042
572/.65 |
| Soggetto topico | Amino acids |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-78423-4
9786612784231 3-527-62126-1 3-527-62127-X |
| Classificazione | 35.62 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ger |
| Nota di contenuto |
Amino Group Chemistry; Contents; Preface; List of Contributors; 1 Simple Molecules, Highly Efficient Amination; 1.1 Introduction; 1.2 Hydroxylamine Derivatives; 1.2.1 O-Sulfonylhydroxylamine; 1.2.2 O-Phosphinylhydroxylamine; 1.2.3 O-Acylhydroxylamine; 1.2.4 O-Trimethylsilylhydroxylamine; 1.2.5 Experimental Procedures; 1.3 Oxime Derivatives; 1.3.1 Synthesis of Primary Amines by Electrophilic Amination of Carbanions; 1.3.2 Experimental Procedures; 1.4 Azo Compounds; 1.4.1 Azodicarboxylates; 1.4.1.1 Allylic Amination through Ene-Type Reactions; 1.4.1.2 Hydrohydrazination of Alkenes
1.4.2 Arylazo Sulfones1.4.3 Experimental Procedures; 1.5 Oxaziridine Derivatives; 1.5.1 Electrophilic Amination of Carbon Nucleophiles; 1.5.2 Amination of Allylic and Propargylic Sulfides by Use of a Ketomalonate-Derived Oxaziridine; 1.5.3 Experimental Procedures; 1.6 Chloramine-T; 1.6.1 Aminochalcogenation of Alkenes; 1.6.2 Aminohydroxylation of Alkenes; 1.6.3 Aziridination of Alkenes; 1.6.4 Other Applications; 1.6.5 Experimental Procedures; 1.7 N-Sulfonyliminophenyliodinane; 1.7.1 Transition Metal-Catalyzed Amination of Alkenes; 1.7.2 Experimental Procedures 1.8 Transition Metal-Nitride Complexes1.8.1 Nitrogen Atom Transfer Mediated by Transition Metal/Nitride Complexes; 1.8.2 Experimental Procedures; 1.9 Azido Derivatives; 1.9.1 Electrophilic Amination of Organometallic Reagents with Organic Azides; 1.9.2 Radical-Mediated Amination with Sulfonyl Azides; 1.9.3 Hydroazidation of Alkenes with Sulfonyl Azides; 1.9.4 Experimental Procedures; 1.10 Gabriel-Type Reagents; 1.10.1 Nucleophilic Amination Reactions; 1.10.2 Experimental Procedure; 1.11 Conclusion; 2 Catalytic C-H Amination with Nitrenes; 2.1 Introduction; 2.2 Historical Overview 2.3 Hypervalent Iodine-Mediated C-H Amination2.3.1 Intramolecular C-H Amination; 2.3.1.1 From NH(2) Carbamates; 2.3.1.2 From NH(2) Sulfamates; 2.3.1.3 From Other Nitrogen Functionalities; 2.3.2 Intermolecular C-H Amination; 2.3.2.1 General Scope and Limitations; 2.3.2.2 Recent Major Improvements; 2.4 Other Nitrene Precursors for C-H Amination; 2.4.1 Azides; 2.4.2 Haloamines; 2.4.3 Carbamate Derivatives; 2.5 Amination of Aromatic C-H Bonds; 2.6 Applications in Total Synthesis; 2.6.1 Application of Intramolecular C-H Amination with Carbamates 2.6.2 Application of Intramolecular C-H Amination with Sulfamates2.6.3 Application of Intermolecular C-H Amination; 2.7 Conclusions; 3 Nitroalkenes as Amination Tools; 3.1 Introduction; 3.2 General Strategies for the Synthesis of Nitroalkenes; 3.3 Synthesis of Alkylamines; 3.3.1 Monoamines; 3.3.2 Amino Acid Derivatives; 3.3.3 Amino Alcohols; 3.3.4 Diamino Derivatives; 3.4 Pyrrolidine Derivatives; 3.4.1 Pyrrolidinones; 3.4.2 Pyrrolidines; 3.5 Piperidines and Piperazines; 3.6 Pyrrolizidines and Related Derivatives; 3.7 Arene-Fused Nitrogen Heterocycles; 3.7.1 Pyrroloindole Derivatives 3.7.2 Carbolines and their Tryptamine Precursors |
| Record Nr. | UNINA-9910144276703321 |
| Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Amino group chemistry : from synthesis to the life sciences / / edited by Alfredo Ricci
| Amino group chemistry : from synthesis to the life sciences / / edited by Alfredo Ricci |
| Pubbl/distr/stampa | Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008 |
| Descrizione fisica | 1 online resource (410 p.) |
| Disciplina |
547.042
572/.65 |
| Soggetto topico | Amino acids |
| ISBN |
1-282-78423-4
9786612784231 3-527-62126-1 3-527-62127-X |
| Classificazione | 35.62 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ger |
| Nota di contenuto |
Amino Group Chemistry; Contents; Preface; List of Contributors; 1 Simple Molecules, Highly Efficient Amination; 1.1 Introduction; 1.2 Hydroxylamine Derivatives; 1.2.1 O-Sulfonylhydroxylamine; 1.2.2 O-Phosphinylhydroxylamine; 1.2.3 O-Acylhydroxylamine; 1.2.4 O-Trimethylsilylhydroxylamine; 1.2.5 Experimental Procedures; 1.3 Oxime Derivatives; 1.3.1 Synthesis of Primary Amines by Electrophilic Amination of Carbanions; 1.3.2 Experimental Procedures; 1.4 Azo Compounds; 1.4.1 Azodicarboxylates; 1.4.1.1 Allylic Amination through Ene-Type Reactions; 1.4.1.2 Hydrohydrazination of Alkenes
1.4.2 Arylazo Sulfones1.4.3 Experimental Procedures; 1.5 Oxaziridine Derivatives; 1.5.1 Electrophilic Amination of Carbon Nucleophiles; 1.5.2 Amination of Allylic and Propargylic Sulfides by Use of a Ketomalonate-Derived Oxaziridine; 1.5.3 Experimental Procedures; 1.6 Chloramine-T; 1.6.1 Aminochalcogenation of Alkenes; 1.6.2 Aminohydroxylation of Alkenes; 1.6.3 Aziridination of Alkenes; 1.6.4 Other Applications; 1.6.5 Experimental Procedures; 1.7 N-Sulfonyliminophenyliodinane; 1.7.1 Transition Metal-Catalyzed Amination of Alkenes; 1.7.2 Experimental Procedures 1.8 Transition Metal-Nitride Complexes1.8.1 Nitrogen Atom Transfer Mediated by Transition Metal/Nitride Complexes; 1.8.2 Experimental Procedures; 1.9 Azido Derivatives; 1.9.1 Electrophilic Amination of Organometallic Reagents with Organic Azides; 1.9.2 Radical-Mediated Amination with Sulfonyl Azides; 1.9.3 Hydroazidation of Alkenes with Sulfonyl Azides; 1.9.4 Experimental Procedures; 1.10 Gabriel-Type Reagents; 1.10.1 Nucleophilic Amination Reactions; 1.10.2 Experimental Procedure; 1.11 Conclusion; 2 Catalytic C-H Amination with Nitrenes; 2.1 Introduction; 2.2 Historical Overview 2.3 Hypervalent Iodine-Mediated C-H Amination2.3.1 Intramolecular C-H Amination; 2.3.1.1 From NH(2) Carbamates; 2.3.1.2 From NH(2) Sulfamates; 2.3.1.3 From Other Nitrogen Functionalities; 2.3.2 Intermolecular C-H Amination; 2.3.2.1 General Scope and Limitations; 2.3.2.2 Recent Major Improvements; 2.4 Other Nitrene Precursors for C-H Amination; 2.4.1 Azides; 2.4.2 Haloamines; 2.4.3 Carbamate Derivatives; 2.5 Amination of Aromatic C-H Bonds; 2.6 Applications in Total Synthesis; 2.6.1 Application of Intramolecular C-H Amination with Carbamates 2.6.2 Application of Intramolecular C-H Amination with Sulfamates2.6.3 Application of Intermolecular C-H Amination; 2.7 Conclusions; 3 Nitroalkenes as Amination Tools; 3.1 Introduction; 3.2 General Strategies for the Synthesis of Nitroalkenes; 3.3 Synthesis of Alkylamines; 3.3.1 Monoamines; 3.3.2 Amino Acid Derivatives; 3.3.3 Amino Alcohols; 3.3.4 Diamino Derivatives; 3.4 Pyrrolidine Derivatives; 3.4.1 Pyrrolidinones; 3.4.2 Pyrrolidines; 3.5 Piperidines and Piperazines; 3.6 Pyrrolizidines and Related Derivatives; 3.7 Arene-Fused Nitrogen Heterocycles; 3.7.1 Pyrroloindole Derivatives 3.7.2 Carbolines and their Tryptamine Precursors |
| Record Nr. | UNINA-9910830098903321 |
| Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Biogenic Amines / / edited by Charalampos Proestos
| Biogenic Amines / / edited by Charalampos Proestos |
| Pubbl/distr/stampa | London, United Kingdom : , : IntechOpen, , 2019 |
| Descrizione fisica | 1 online resource (88 pages) |
| Disciplina | 547.042 |
| Soggetto topico | Biogenic amines |
| ISBN |
1-83962-090-0
1-78984-134-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910317956203321 |
| London, United Kingdom : , : IntechOpen, , 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chemoselective Nucleophilic α-Amination of Amides / / by Miran Lemmerer
| Chemoselective Nucleophilic α-Amination of Amides / / by Miran Lemmerer |
| Autore | Lemmerer Miran |
| Edizione | [1st ed. 2020.] |
| Pubbl/distr/stampa | Wiesbaden : , : Springer Fachmedien Wiesbaden : , : Imprint : Springer Spektrum, , 2020 |
| Descrizione fisica | 1 online resource (68 pages) |
| Disciplina | 547.042 |
| Collana | BestMasters |
| Soggetto topico |
Asymmetric synthesis
Chemical structure Organic compounds - Synthesis Chemistry Asymmetric Synthesis Structure And Bonding Synthetic Chemistry Methodology Reactive Precursor |
| ISBN | 3-658-30020-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Traditional Umpolung Reactions in Organic Chemistry -- Insight into Electrophilic Amide Activation -- Results and Discussion of a New α-Amination Method via Umpolung of Amides -- α-Arylation of Carbonlys via a Smiles Rearrangement. |
| Record Nr. | UNINA-9910410046703321 |
|
Lemmerer Miran
|
||
| Wiesbaden : , : Springer Fachmedien Wiesbaden : , : Imprint : Springer Spektrum, , 2020 | ||
| 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 |
| 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 | ||
| ||
Formation, structure and properties of enzyme resistant starch : dissertationes de agricultura / Relinde Eerlingen
| Formation, structure and properties of enzyme resistant starch : dissertationes de agricultura / Relinde Eerlingen |
| Autore | Eerlingen, Relinde |
| Pubbl/distr/stampa | Leuven : Katholieke Universiteit, 1994 |
| Descrizione fisica | 135 p. ; 24 cm |
| Disciplina | 547.042 |
| Soggetto non controllato |
Amido
Enzimi |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ita |
| Record Nr. | UNINA-990001785690403321 |
|
Eerlingen, Relinde
|
||
| Leuven : Katholieke Universiteit, 1994 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
