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Organic reactions in water [[electronic resource] ] : principles, strategies and applications / / edited by U. Marcus Lindström
| Organic reactions in water [[electronic resource] ] : principles, strategies and applications / / edited by U. Marcus Lindström |
| Pubbl/distr/stampa | Oxford ; ; Ames, Iowa, : Blackwell Pub., 2007 |
| Descrizione fisica | 1 online resource (424 p.) |
| Disciplina |
547.2
547/.2 |
| Altri autori (Persone) | LindströmU. Marcus <1971-> (Ulf Marcus) |
| Soggetto topico |
Water chemistry
Solvents - Environmental aspects Organic compounds - Synthesis - Environmental aspects |
| ISBN |
1-281-32026-9
9786611320263 0-470-98881-9 0-470-99424-X |
| Classificazione |
35.52
35.51 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Organic Reactions in Water : Principles, Strategies and Applications; Contents; Contributors; Preface; Foreword; 1 A Fifty-Year Perspective on Chemistry in Water; 1.1 Enzyme mimics and models; 1.1.1 Thiamine; 1.1.2 Cyclodextrins; 1.1.3 Cyclodextrins with bound metal ions; 1.1.4 Cyclodextrin dimers; 1.1.5 Ribonuclease mimics; 1.1.6 Transaminase mimics; 1.1.7 Cytochrome P-450 mimics; 1.2 Reactions in water promoted by hydrophobic binding of small molecules; 1.2.1 Diels-Alder reactions; 1.2.2 The benzoin condensation; 1.2.3 Atom transfer reactions
1.3 Quantitative antihydrophobic effects in water and the geometries of transition states1.4 The importance of water as a reaction solvent; References; 2 Structure and Properties of Water; 2.1 Water, the molecule and the liquid; 2.1.1 The single water molecule; 2.1.2 Liquid water; 2.2 Properties of water; 2.2.1 Solvent properties and parameters; 2.2.2 Thermodynamics of hydration; 2.2.3 Hydrophobic interactions; 2.3 Kinetic solvent effects in aqueous solution; References; 3 Acid Catalysis in Water; 3.1 Homogeneous catalysis; 3.1.1 Bronsted acid catalysis; 3.1.2 Lewis acid catalysis 3.1.3 Asymmetric catalysis3.2 Heterogeneous catalysis; 3.2.1 Polymer-supported Bronsted catalysis; 3.2.2 Polymer-supported metal catalysis; 3.3 Micellar catalysis; 3.3.1 LASC (Lewis acid-surfactant-combined catalysts); 3.3.2 BASC (Bronsted acid-surfactant-combined catalyst); 3.4 Conclusion; References; 4 Metal-Mediated C-C Bond Formations in Aqueous Media; 4.1 Introduction; 4.2 Reactivity of organometallic compounds with water; 4.2.1 C-M bonding; 4.2.2 C-M hydrolysis; 4.2.3 C M-reactions; 4.2.4 C-C bond formations via C-M reactions in water; 4.3 Allylation of carbonyls and imines 4.3.1 Alyllation of carbonyl compounds4.3.2 Allylation of imines and related compounds; 4.4 Propargylation/allenylation of carbonyls, imines, and related compounds; 4.5 Metal-mediated benzylation of carbonyls and imines; 4.6 Arylation and vinylation of carbonyls and imines; 4.6.1 Arylation and vinylation of aldehydes; 4.6.2 Arylation and vinylation of imines and related compounds; 4.7 Alkynylation of carbonyls, imines, and related compounds; 4.7.1 Alkynylation of aldehydes; 4.7.2 Alkynylation of imines and related compounds; 4.7.3 Asymmetric alkynylation 4.8 Metal-mediated aldol and Reformatsky-type reactions4.9 Metal-mediated alkylation of carbonyls and imines; 4.9.1 Alkylation of aldehydes; 4.9.2 Alkylation of imines; 4.10 Metal-mediated conjugate addition reactions; 4.10.1 Addition of alkyl groups; 4.10.2 Addition of vinyl and aryl groups; 4.10.3 Addition of alkynes; 4.11 Metal-mediated coupling reactions; 4.11.1 Pinacol coupling; 4.11.2 Other reductive couplings; 4.11.3 Cross-dehydrogenative coupling; 4.12 Conclusion; References; 5 Pericyclic Reactions in Aqueous Media; 5.1 Diels-Alder cycloaddition reactions 5.1.1 Carbo Diels-Alder reactions |
| Record Nr. | UNISA-996203979703316 |
| Oxford ; ; Ames, Iowa, : Blackwell Pub., 2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Organic reactions in water [[electronic resource] ] : principles, strategies and applications / / edited by U. Marcus Lindström
| Organic reactions in water [[electronic resource] ] : principles, strategies and applications / / edited by U. Marcus Lindström |
| Pubbl/distr/stampa | Oxford ; ; Ames, Iowa, : Blackwell Pub., 2007 |
| Descrizione fisica | 1 online resource (424 p.) |
| Disciplina |
547.2
547/.2 |
| Altri autori (Persone) | LindströmU. Marcus <1971-> (Ulf Marcus) |
| Soggetto topico |
Water chemistry
Solvents - Environmental aspects Organic compounds - Synthesis - Environmental aspects |
| ISBN |
1-281-32026-9
9786611320263 0-470-98881-9 0-470-99424-X |
| Classificazione |
35.52
35.51 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Organic Reactions in Water : Principles, Strategies and Applications; Contents; Contributors; Preface; Foreword; 1 A Fifty-Year Perspective on Chemistry in Water; 1.1 Enzyme mimics and models; 1.1.1 Thiamine; 1.1.2 Cyclodextrins; 1.1.3 Cyclodextrins with bound metal ions; 1.1.4 Cyclodextrin dimers; 1.1.5 Ribonuclease mimics; 1.1.6 Transaminase mimics; 1.1.7 Cytochrome P-450 mimics; 1.2 Reactions in water promoted by hydrophobic binding of small molecules; 1.2.1 Diels-Alder reactions; 1.2.2 The benzoin condensation; 1.2.3 Atom transfer reactions
1.3 Quantitative antihydrophobic effects in water and the geometries of transition states1.4 The importance of water as a reaction solvent; References; 2 Structure and Properties of Water; 2.1 Water, the molecule and the liquid; 2.1.1 The single water molecule; 2.1.2 Liquid water; 2.2 Properties of water; 2.2.1 Solvent properties and parameters; 2.2.2 Thermodynamics of hydration; 2.2.3 Hydrophobic interactions; 2.3 Kinetic solvent effects in aqueous solution; References; 3 Acid Catalysis in Water; 3.1 Homogeneous catalysis; 3.1.1 Bronsted acid catalysis; 3.1.2 Lewis acid catalysis 3.1.3 Asymmetric catalysis3.2 Heterogeneous catalysis; 3.2.1 Polymer-supported Bronsted catalysis; 3.2.2 Polymer-supported metal catalysis; 3.3 Micellar catalysis; 3.3.1 LASC (Lewis acid-surfactant-combined catalysts); 3.3.2 BASC (Bronsted acid-surfactant-combined catalyst); 3.4 Conclusion; References; 4 Metal-Mediated C-C Bond Formations in Aqueous Media; 4.1 Introduction; 4.2 Reactivity of organometallic compounds with water; 4.2.1 C-M bonding; 4.2.2 C-M hydrolysis; 4.2.3 C M-reactions; 4.2.4 C-C bond formations via C-M reactions in water; 4.3 Allylation of carbonyls and imines 4.3.1 Alyllation of carbonyl compounds4.3.2 Allylation of imines and related compounds; 4.4 Propargylation/allenylation of carbonyls, imines, and related compounds; 4.5 Metal-mediated benzylation of carbonyls and imines; 4.6 Arylation and vinylation of carbonyls and imines; 4.6.1 Arylation and vinylation of aldehydes; 4.6.2 Arylation and vinylation of imines and related compounds; 4.7 Alkynylation of carbonyls, imines, and related compounds; 4.7.1 Alkynylation of aldehydes; 4.7.2 Alkynylation of imines and related compounds; 4.7.3 Asymmetric alkynylation 4.8 Metal-mediated aldol and Reformatsky-type reactions4.9 Metal-mediated alkylation of carbonyls and imines; 4.9.1 Alkylation of aldehydes; 4.9.2 Alkylation of imines; 4.10 Metal-mediated conjugate addition reactions; 4.10.1 Addition of alkyl groups; 4.10.2 Addition of vinyl and aryl groups; 4.10.3 Addition of alkynes; 4.11 Metal-mediated coupling reactions; 4.11.1 Pinacol coupling; 4.11.2 Other reductive couplings; 4.11.3 Cross-dehydrogenative coupling; 4.12 Conclusion; References; 5 Pericyclic Reactions in Aqueous Media; 5.1 Diels-Alder cycloaddition reactions 5.1.1 Carbo Diels-Alder reactions |
| Record Nr. | UNINA-9910830256103321 |
| Oxford ; ; Ames, Iowa, : Blackwell Pub., 2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic reactions in water [[electronic resource] ] : principles, strategies and applications / / edited by U. Marcus Lindström
| Organic reactions in water [[electronic resource] ] : principles, strategies and applications / / edited by U. Marcus Lindström |
| Pubbl/distr/stampa | Oxford ; ; Ames, Iowa, : Blackwell Pub., 2007 |
| Descrizione fisica | 1 online resource (424 p.) |
| Disciplina |
547.2
547/.2 |
| Altri autori (Persone) | LindströmU. Marcus <1971-> (Ulf Marcus) |
| Soggetto topico |
Water chemistry
Solvents - Environmental aspects Organic compounds - Synthesis - Environmental aspects |
| ISBN |
1-281-32026-9
9786611320263 0-470-98881-9 0-470-99424-X |
| Classificazione |
35.52
35.51 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Organic Reactions in Water : Principles, Strategies and Applications; Contents; Contributors; Preface; Foreword; 1 A Fifty-Year Perspective on Chemistry in Water; 1.1 Enzyme mimics and models; 1.1.1 Thiamine; 1.1.2 Cyclodextrins; 1.1.3 Cyclodextrins with bound metal ions; 1.1.4 Cyclodextrin dimers; 1.1.5 Ribonuclease mimics; 1.1.6 Transaminase mimics; 1.1.7 Cytochrome P-450 mimics; 1.2 Reactions in water promoted by hydrophobic binding of small molecules; 1.2.1 Diels-Alder reactions; 1.2.2 The benzoin condensation; 1.2.3 Atom transfer reactions
1.3 Quantitative antihydrophobic effects in water and the geometries of transition states1.4 The importance of water as a reaction solvent; References; 2 Structure and Properties of Water; 2.1 Water, the molecule and the liquid; 2.1.1 The single water molecule; 2.1.2 Liquid water; 2.2 Properties of water; 2.2.1 Solvent properties and parameters; 2.2.2 Thermodynamics of hydration; 2.2.3 Hydrophobic interactions; 2.3 Kinetic solvent effects in aqueous solution; References; 3 Acid Catalysis in Water; 3.1 Homogeneous catalysis; 3.1.1 Bronsted acid catalysis; 3.1.2 Lewis acid catalysis 3.1.3 Asymmetric catalysis3.2 Heterogeneous catalysis; 3.2.1 Polymer-supported Bronsted catalysis; 3.2.2 Polymer-supported metal catalysis; 3.3 Micellar catalysis; 3.3.1 LASC (Lewis acid-surfactant-combined catalysts); 3.3.2 BASC (Bronsted acid-surfactant-combined catalyst); 3.4 Conclusion; References; 4 Metal-Mediated C-C Bond Formations in Aqueous Media; 4.1 Introduction; 4.2 Reactivity of organometallic compounds with water; 4.2.1 C-M bonding; 4.2.2 C-M hydrolysis; 4.2.3 C M-reactions; 4.2.4 C-C bond formations via C-M reactions in water; 4.3 Allylation of carbonyls and imines 4.3.1 Alyllation of carbonyl compounds4.3.2 Allylation of imines and related compounds; 4.4 Propargylation/allenylation of carbonyls, imines, and related compounds; 4.5 Metal-mediated benzylation of carbonyls and imines; 4.6 Arylation and vinylation of carbonyls and imines; 4.6.1 Arylation and vinylation of aldehydes; 4.6.2 Arylation and vinylation of imines and related compounds; 4.7 Alkynylation of carbonyls, imines, and related compounds; 4.7.1 Alkynylation of aldehydes; 4.7.2 Alkynylation of imines and related compounds; 4.7.3 Asymmetric alkynylation 4.8 Metal-mediated aldol and Reformatsky-type reactions4.9 Metal-mediated alkylation of carbonyls and imines; 4.9.1 Alkylation of aldehydes; 4.9.2 Alkylation of imines; 4.10 Metal-mediated conjugate addition reactions; 4.10.1 Addition of alkyl groups; 4.10.2 Addition of vinyl and aryl groups; 4.10.3 Addition of alkynes; 4.11 Metal-mediated coupling reactions; 4.11.1 Pinacol coupling; 4.11.2 Other reductive couplings; 4.11.3 Cross-dehydrogenative coupling; 4.12 Conclusion; References; 5 Pericyclic Reactions in Aqueous Media; 5.1 Diels-Alder cycloaddition reactions 5.1.1 Carbo Diels-Alder reactions |
| Record Nr. | UNINA-9910841876403321 |
| Oxford ; ; Ames, Iowa, : Blackwell Pub., 2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic syntheses based on name reactions [[electronic resource] ] : a practical guide to over 750 transformations / / A. Hassner, I. Namboothiri
| Organic syntheses based on name reactions [[electronic resource] ] : a practical guide to over 750 transformations / / A. Hassner, I. Namboothiri |
| Autore | Hassner Alfred |
| Edizione | [3rd ed.] |
| Pubbl/distr/stampa | Oxford, : Elsevier, 2012 |
| Descrizione fisica | 1 online resource (612 p.) |
| Disciplina |
547.2
547/.2 |
| Altri autori (Persone) | NamboothiriI |
| Soggetto topico | Organic compounds - Synthesis |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-283-34773-3
9786613347732 0-08-096631-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Organic Syntheses Basedon Name Reactions: A Practical Guide to 750 Transformations; Copyright; Contents; Foreword by D. Seebach; Foreword by S. Danishefsky; Preface to the Third Edition; Preface to the Second Edition; Preface to the First Edition; An Overview of Synthesis Related Name Reactions; Overview - Pd Catalyzed C-C Coupling Name Reactions; List of Abbreviations; ABIKO-MASAMUNE Asymmetric Aldol Reaction; ABRAMOV Asymmetric Phosphonylation; ACHMATOWICZ Furanylcarbinol Rearrangement; ACYLOIN Rearrangement; ADLER Phenol Oxidation; ALDER (Ene) Reaction
ALDER-RICKERT Acetylene CycloadditionALDOL Reactions; ALLEN Phosphonium Rearrangement; ALPER Carbonylation; AMADORI Glucosamine Rearrangement; ANGELI-RIMINI Hydroxamic Acid Synthesis; APPEL Displacement Reagent; ARBUZOV Phosphonate Synthesis; ARNDT-EISTERT RCOOH Homologation; ASINGER Thiazoline Synthesis; ATHERTON-TODD Phosphoramidate Synthesis; AUWERS Flavone Synthesis; AUWERS-INHOFFEN Dienone-Phenol Rearrangement; BAER-FISCHER Amino Sugar Synthesis; BAEYER Pyridine Synthesis; BAEYER Diarylmethane Synthesis; BAEYER-DREWSON Indoxyl Synthesis; BAEYER Oxindole Synthesis BAEYER-VILLIGER Aromatic TritylationBAEYER-VILLIGER Ketone Oxidation; BAILEY Crisscross Cycloaddition; BAKER-VENKATARAMAN Flavone Synthesis; BALABAN Pyrylium Salt Synthesis; BALLY-SCHOLL Benzanthrene Synthesis; BALSON Aromatic Alkylation; BAMBERGER Benzotriazine Synthesis; BAMBERGER Imidazole Cleavage; BAMFORD-STEVENS Tosylhydrazone Decomposition; BARBAS-LIST Asymmetric Michael Reaction; BARBIER In Situ Grignard Reaction; BARBIER-WIELAND Ester Chain Degradation; BARDHAN-SENGUPTA Phenanthrene Synthesis; BARGELLINI 3-Component Carboxylic Acid Synthesis; BARLUENGA Iodination Reagent BARTON ArylationBARTON Deamination; BARTON Decarboxylation; BARTON Nitrite Photolysis; BARTON-KELLOG Olefination; BARTON-McCOMBIE Alcohol Deoxygenation; BART-SCHELLER Aromatic Arsonylation; BAUDISCH Nitrosophenol Synthesis; BECHAMP Phenol, Aniline Arsonilation; BECKMANN Oxime Rearrangement or Fragmentation; BELLER Multicomponent Amino Acid Synthesis; BENARY Conjugated Aldehyde Synthesis; BERCHTOLD Enamine Homologation; BERGMAN Cycloaromatization; BERNTHSEN Acridine Synthesis; BERTRAND-STEPHAN Metal-free Bond Activation; BESTMANN Cumulene Ylides; BIGINELLI Pyrimidone Synthesis BIRCH Na-NH3 ReductionBISCHLER Benzotriazine Synthesis; BISCHLER-MOHLAU Indole Synthesis; BISCHLER-NAPIERALSKI Isoquinoline Synthesis; BLACK Enol Carbonate Rearrangement; BLANC-QUELLET Chloroalkylation; BLICKE-PACHTER Pteridines Synthesis; BLOMQUIST Macrocycles Synthesis; BLUM Aziridine Synthesis; BODROUX-CHICHIBABIN Aromatic Aldehyde Synthesis; BOEKELHEIDE Dipole Ring Expansions; BOGER Thermal Cycloadditions; BOGER N-Heterocycles by Reverse Demand Diels-Alder; BOORD Enol Ether Synthesis; BORCH Reductive Amination; BORSCHE-BEECH Aromatic Aldehyde Synthesis BOULTON-KATRITZKY Heterocyclic Rearrangement |
| Record Nr. | UNINA-9910457790103321 |
Hassner Alfred
|
||
| Oxford, : Elsevier, 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic syntheses based on name reactions [[electronic resource] ] : a practical guide to over 750 transformations / / A. Hassner, I. Namboothiri
| Organic syntheses based on name reactions [[electronic resource] ] : a practical guide to over 750 transformations / / A. Hassner, I. Namboothiri |
| Autore | Hassner Alfred |
| Edizione | [3rd ed.] |
| Pubbl/distr/stampa | Oxford, : Elsevier, 2012 |
| Descrizione fisica | 1 online resource (612 p.) |
| Disciplina |
547.2
547/.2 |
| Altri autori (Persone) | NamboothiriI |
| Soggetto topico | Organic compounds - Synthesis |
| ISBN |
1-283-34773-3
9786613347732 0-08-096631-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Organic Syntheses Basedon Name Reactions: A Practical Guide to 750 Transformations; Copyright; Contents; Foreword by D. Seebach; Foreword by S. Danishefsky; Preface to the Third Edition; Preface to the Second Edition; Preface to the First Edition; An Overview of Synthesis Related Name Reactions; Overview - Pd Catalyzed C-C Coupling Name Reactions; List of Abbreviations; ABIKO-MASAMUNE Asymmetric Aldol Reaction; ABRAMOV Asymmetric Phosphonylation; ACHMATOWICZ Furanylcarbinol Rearrangement; ACYLOIN Rearrangement; ADLER Phenol Oxidation; ALDER (Ene) Reaction
ALDER-RICKERT Acetylene CycloadditionALDOL Reactions; ALLEN Phosphonium Rearrangement; ALPER Carbonylation; AMADORI Glucosamine Rearrangement; ANGELI-RIMINI Hydroxamic Acid Synthesis; APPEL Displacement Reagent; ARBUZOV Phosphonate Synthesis; ARNDT-EISTERT RCOOH Homologation; ASINGER Thiazoline Synthesis; ATHERTON-TODD Phosphoramidate Synthesis; AUWERS Flavone Synthesis; AUWERS-INHOFFEN Dienone-Phenol Rearrangement; BAER-FISCHER Amino Sugar Synthesis; BAEYER Pyridine Synthesis; BAEYER Diarylmethane Synthesis; BAEYER-DREWSON Indoxyl Synthesis; BAEYER Oxindole Synthesis BAEYER-VILLIGER Aromatic TritylationBAEYER-VILLIGER Ketone Oxidation; BAILEY Crisscross Cycloaddition; BAKER-VENKATARAMAN Flavone Synthesis; BALABAN Pyrylium Salt Synthesis; BALLY-SCHOLL Benzanthrene Synthesis; BALSON Aromatic Alkylation; BAMBERGER Benzotriazine Synthesis; BAMBERGER Imidazole Cleavage; BAMFORD-STEVENS Tosylhydrazone Decomposition; BARBAS-LIST Asymmetric Michael Reaction; BARBIER In Situ Grignard Reaction; BARBIER-WIELAND Ester Chain Degradation; BARDHAN-SENGUPTA Phenanthrene Synthesis; BARGELLINI 3-Component Carboxylic Acid Synthesis; BARLUENGA Iodination Reagent BARTON ArylationBARTON Deamination; BARTON Decarboxylation; BARTON Nitrite Photolysis; BARTON-KELLOG Olefination; BARTON-McCOMBIE Alcohol Deoxygenation; BART-SCHELLER Aromatic Arsonylation; BAUDISCH Nitrosophenol Synthesis; BECHAMP Phenol, Aniline Arsonilation; BECKMANN Oxime Rearrangement or Fragmentation; BELLER Multicomponent Amino Acid Synthesis; BENARY Conjugated Aldehyde Synthesis; BERCHTOLD Enamine Homologation; BERGMAN Cycloaromatization; BERNTHSEN Acridine Synthesis; BERTRAND-STEPHAN Metal-free Bond Activation; BESTMANN Cumulene Ylides; BIGINELLI Pyrimidone Synthesis BIRCH Na-NH3 ReductionBISCHLER Benzotriazine Synthesis; BISCHLER-MOHLAU Indole Synthesis; BISCHLER-NAPIERALSKI Isoquinoline Synthesis; BLACK Enol Carbonate Rearrangement; BLANC-QUELLET Chloroalkylation; BLICKE-PACHTER Pteridines Synthesis; BLOMQUIST Macrocycles Synthesis; BLUM Aziridine Synthesis; BODROUX-CHICHIBABIN Aromatic Aldehyde Synthesis; BOEKELHEIDE Dipole Ring Expansions; BOGER Thermal Cycloadditions; BOGER N-Heterocycles by Reverse Demand Diels-Alder; BOORD Enol Ether Synthesis; BORCH Reductive Amination; BORSCHE-BEECH Aromatic Aldehyde Synthesis BOULTON-KATRITZKY Heterocyclic Rearrangement |
| Record Nr. | UNINA-9910781531303321 |
|
Hassner Alfred
|
||
| Oxford, : Elsevier, 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic syntheses based on name reactions [[electronic resource] ] : a practical guide to over 750 transformations / / A. Hassner, I. Namboothiri
| Organic syntheses based on name reactions [[electronic resource] ] : a practical guide to over 750 transformations / / A. Hassner, I. Namboothiri |
| Autore | Hassner Alfred |
| Edizione | [3rd ed.] |
| Pubbl/distr/stampa | Oxford, : Elsevier, 2012 |
| Descrizione fisica | 1 online resource (612 p.) |
| Disciplina |
547.2
547/.2 |
| Altri autori (Persone) | NamboothiriI |
| Soggetto topico | Organic compounds - Synthesis |
| ISBN |
1-283-34773-3
9786613347732 0-08-096631-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Organic Syntheses Basedon Name Reactions: A Practical Guide to 750 Transformations; Copyright; Contents; Foreword by D. Seebach; Foreword by S. Danishefsky; Preface to the Third Edition; Preface to the Second Edition; Preface to the First Edition; An Overview of Synthesis Related Name Reactions; Overview - Pd Catalyzed C-C Coupling Name Reactions; List of Abbreviations; ABIKO-MASAMUNE Asymmetric Aldol Reaction; ABRAMOV Asymmetric Phosphonylation; ACHMATOWICZ Furanylcarbinol Rearrangement; ACYLOIN Rearrangement; ADLER Phenol Oxidation; ALDER (Ene) Reaction
ALDER-RICKERT Acetylene CycloadditionALDOL Reactions; ALLEN Phosphonium Rearrangement; ALPER Carbonylation; AMADORI Glucosamine Rearrangement; ANGELI-RIMINI Hydroxamic Acid Synthesis; APPEL Displacement Reagent; ARBUZOV Phosphonate Synthesis; ARNDT-EISTERT RCOOH Homologation; ASINGER Thiazoline Synthesis; ATHERTON-TODD Phosphoramidate Synthesis; AUWERS Flavone Synthesis; AUWERS-INHOFFEN Dienone-Phenol Rearrangement; BAER-FISCHER Amino Sugar Synthesis; BAEYER Pyridine Synthesis; BAEYER Diarylmethane Synthesis; BAEYER-DREWSON Indoxyl Synthesis; BAEYER Oxindole Synthesis BAEYER-VILLIGER Aromatic TritylationBAEYER-VILLIGER Ketone Oxidation; BAILEY Crisscross Cycloaddition; BAKER-VENKATARAMAN Flavone Synthesis; BALABAN Pyrylium Salt Synthesis; BALLY-SCHOLL Benzanthrene Synthesis; BALSON Aromatic Alkylation; BAMBERGER Benzotriazine Synthesis; BAMBERGER Imidazole Cleavage; BAMFORD-STEVENS Tosylhydrazone Decomposition; BARBAS-LIST Asymmetric Michael Reaction; BARBIER In Situ Grignard Reaction; BARBIER-WIELAND Ester Chain Degradation; BARDHAN-SENGUPTA Phenanthrene Synthesis; BARGELLINI 3-Component Carboxylic Acid Synthesis; BARLUENGA Iodination Reagent BARTON ArylationBARTON Deamination; BARTON Decarboxylation; BARTON Nitrite Photolysis; BARTON-KELLOG Olefination; BARTON-McCOMBIE Alcohol Deoxygenation; BART-SCHELLER Aromatic Arsonylation; BAUDISCH Nitrosophenol Synthesis; BECHAMP Phenol, Aniline Arsonilation; BECKMANN Oxime Rearrangement or Fragmentation; BELLER Multicomponent Amino Acid Synthesis; BENARY Conjugated Aldehyde Synthesis; BERCHTOLD Enamine Homologation; BERGMAN Cycloaromatization; BERNTHSEN Acridine Synthesis; BERTRAND-STEPHAN Metal-free Bond Activation; BESTMANN Cumulene Ylides; BIGINELLI Pyrimidone Synthesis BIRCH Na-NH3 ReductionBISCHLER Benzotriazine Synthesis; BISCHLER-MOHLAU Indole Synthesis; BISCHLER-NAPIERALSKI Isoquinoline Synthesis; BLACK Enol Carbonate Rearrangement; BLANC-QUELLET Chloroalkylation; BLICKE-PACHTER Pteridines Synthesis; BLOMQUIST Macrocycles Synthesis; BLUM Aziridine Synthesis; BODROUX-CHICHIBABIN Aromatic Aldehyde Synthesis; BOEKELHEIDE Dipole Ring Expansions; BOGER Thermal Cycloadditions; BOGER N-Heterocycles by Reverse Demand Diels-Alder; BOORD Enol Ether Synthesis; BORCH Reductive Amination; BORSCHE-BEECH Aromatic Aldehyde Synthesis BOULTON-KATRITZKY Heterocyclic Rearrangement |
| Record Nr. | UNINA-9910814672603321 |
|
Hassner Alfred
|
||
| Oxford, : Elsevier, 2012 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic synthesis [[electronic resource] /] / Michael B. Smith
| Organic synthesis [[electronic resource] /] / Michael B. Smith |
| Autore | Smith Michael <1946 October 17-> |
| Edizione | [3rd ed.] |
| Pubbl/distr/stampa | [Boston], : Academic Press, an imprint of Elsevier, [2011] |
| Descrizione fisica | 1 online resource (1536 p.) |
| Disciplina | 547/.2 |
| Soggetto topico | Organic compounds - Synthesis |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-58131-X
9786613611093 0-12-415884-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Organic Synthesis; Copyright Page; About the Author; Table of Contents; Preface to the 3rd edition; Preface to the 1st edition. Why I wrote this book!; Common Abbreviations; Chapter 1: Retrosynthesis, Stereochemistry, and Conformations; 1.1. Introduction; 1.2. The Disconnection Protocol; 1.3. Bond Proximity and Implications for Chemical Reactions; 1.4. Stereochemistry; 1.5. Conformations; 1.6. Conclusion; Homework; Chapter 2: Acids, Bases and Functional Group Exchange Reactions; 2.1. Introduction; 2.2. Brønsted-Lowry Acids and Bases; 2.3. Lewis Acids
4.6. Borane, Aluminum Hydride, and Derivatives4.7. Stereoselectivity in Reductions; 4.8. Catalytic Hydrogenation; 4.9. Dissolving Metal Reductions; 4.10. Nonmetallic Reducing Agents; 4.11. Conclusion; Homework; Chapter 5 : Hydroboration; 5.1. Introduction; 5.2. Preparation of Alkyl and Alkenyl Boranes; 5.3. Synthetic Transformations; 5.4. Formation of Oxygen-Containing Functional Groups; 5.5. Amines and Sulfides via Hydroboration; 5.6. Conclusion; Homework; Chapter 6 : Stereocontrol and Ring Formation; 6.1. Introduction; 6.2. Stereocontrol in AcyclIc Systems 8.5. OrganoLithium Reagents (C-Li) |
| Record Nr. | UNINA-9910461489703321 |
|
Smith Michael <1946 October 17->
|
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| [Boston], : Academic Press, an imprint of Elsevier, [2011] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic synthesis [[electronic resource] /] / Michael B. Smith
| Organic synthesis [[electronic resource] /] / Michael B. Smith |
| Autore | Smith Michael <1946 October 17-> |
| Edizione | [3rd ed.] |
| Pubbl/distr/stampa | [Boston], : Academic Press, an imprint of Elsevier, [2011] |
| Descrizione fisica | 1 online resource (1536 p.) |
| Disciplina | 547/.2 |
| Soggetto topico | Organic compounds - Synthesis |
| ISBN |
1-280-58131-X
9786613611093 0-12-415884-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Organic Synthesis; Copyright Page; About the Author; Table of Contents; Preface to the 3rd edition; Preface to the 1st edition. Why I wrote this book!; Common Abbreviations; Chapter 1: Retrosynthesis, Stereochemistry, and Conformations; 1.1. Introduction; 1.2. The Disconnection Protocol; 1.3. Bond Proximity and Implications for Chemical Reactions; 1.4. Stereochemistry; 1.5. Conformations; 1.6. Conclusion; Homework; Chapter 2: Acids, Bases and Functional Group Exchange Reactions; 2.1. Introduction; 2.2. Brønsted-Lowry Acids and Bases; 2.3. Lewis Acids
4.6. Borane, Aluminum Hydride, and Derivatives4.7. Stereoselectivity in Reductions; 4.8. Catalytic Hydrogenation; 4.9. Dissolving Metal Reductions; 4.10. Nonmetallic Reducing Agents; 4.11. Conclusion; Homework; Chapter 5 : Hydroboration; 5.1. Introduction; 5.2. Preparation of Alkyl and Alkenyl Boranes; 5.3. Synthetic Transformations; 5.4. Formation of Oxygen-Containing Functional Groups; 5.5. Amines and Sulfides via Hydroboration; 5.6. Conclusion; Homework; Chapter 6 : Stereocontrol and Ring Formation; 6.1. Introduction; 6.2. Stereocontrol in AcyclIc Systems 8.5. OrganoLithium Reagents (C-Li) |
| Record Nr. | UNINA-9910790466603321 |
|
Smith Michael <1946 October 17->
|
||
| [Boston], : Academic Press, an imprint of Elsevier, [2011] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic synthesis / / Michael B. Smith
| Organic synthesis / / Michael B. Smith |
| Autore | Smith Michael <1946 October 17-> |
| Edizione | [3rd ed.] |
| Pubbl/distr/stampa | [Boston], : Academic Press, an imprint of Elsevier, [2011] |
| Descrizione fisica | 1 online resource (1536 p.) |
| Disciplina | 547/.2 |
| Soggetto topico | Organic compounds - Synthesis |
| ISBN |
1-280-58131-X
9786613611093 0-12-415884-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Organic Synthesis; Copyright Page; About the Author; Table of Contents; Preface to the 3rd edition; Preface to the 1st edition. Why I wrote this book!; Common Abbreviations; Chapter 1: Retrosynthesis, Stereochemistry, and Conformations; 1.1. Introduction; 1.2. The Disconnection Protocol; 1.3. Bond Proximity and Implications for Chemical Reactions; 1.4. Stereochemistry; 1.5. Conformations; 1.6. Conclusion; Homework; Chapter 2: Acids, Bases and Functional Group Exchange Reactions; 2.1. Introduction; 2.2. Brønsted-Lowry Acids and Bases; 2.3. Lewis Acids
4.6. Borane, Aluminum Hydride, and Derivatives4.7. Stereoselectivity in Reductions; 4.8. Catalytic Hydrogenation; 4.9. Dissolving Metal Reductions; 4.10. Nonmetallic Reducing Agents; 4.11. Conclusion; Homework; Chapter 5 : Hydroboration; 5.1. Introduction; 5.2. Preparation of Alkyl and Alkenyl Boranes; 5.3. Synthetic Transformations; 5.4. Formation of Oxygen-Containing Functional Groups; 5.5. Amines and Sulfides via Hydroboration; 5.6. Conclusion; Homework; Chapter 6 : Stereocontrol and Ring Formation; 6.1. Introduction; 6.2. Stereocontrol in AcyclIc Systems 8.5. OrganoLithium Reagents (C-Li) |
| Record Nr. | UNINA-9910820073903321 |
|
Smith Michael <1946 October 17->
|
||
| [Boston], : Academic Press, an imprint of Elsevier, [2011] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Organic synthesis [[electronic resource] ] : state of the art 2007-2009 / / Douglass F. Taber
| Organic synthesis [[electronic resource] ] : state of the art 2007-2009 / / Douglass F. Taber |
| Autore | Taber D. F (Douglass F.), <1948-> |
| Pubbl/distr/stampa | Oxford ; ; New York, : Oxford University Press, 2011 |
| Descrizione fisica | 1 online resource (253 p.) |
| Disciplina | 547/.2 |
| Collana | Oxford scholarship online |
| Soggetto topico | Organic compounds - Synthesis - Research |
| Soggetto genere / forma | Electronic books. |
| ISBN |
0-19-756309-0
1-283-23231-6 9786613232311 0-19-984239-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Contents; Preface; Organic Functional Group Interconversion and Protection; 1. Best Synthetic Methods: Oxidation and Reduction; 2. Functional Group Transformations; 3. Best Synthetic Methods: Oxidation; 4. Best Synthetic Methods: Reduction; 5. Best Synthetic Methods: Functional Group Transformation; 6. New Methods for Functional Group Conversion; 7. Organic Functional Group Interconversion: (-)-β-Conhydrine (Barua) and (+)-6'-Hydroxyarenarol (Anderson); 8. New Methods for Functional Group Conversion; 9. Protection of Organic Functional Groups
10. Best Synthetic Methods: Functional Group Protection11. Functional Group Protection; C-H Functionalization; 12. Intermolecular and Intramolecular C-H Functionalization; 13. C-H Functionalization to Form C-O, C-N, and C-C Bonds; 14. Functionalization of C-H Bonds: The Baran Synthesis of Dihydroxyeudesmane; Carbon-Carbon Bond Construction; 15. New Methods for Carbon-Carbon Bond Construction; 16. Best Synthetic Methods: Carbon-Carbon Bond Construction; 17. C-C Single Bond Construction; 18. Construction of Alkenes, Alkynes and Allenes; Reactions of Alkenes 19. Reduction, Oxidation and Homologation of Alkenes20. Reactions of Alkenes; 21. Selective Reactions of Alkenes; Alkene and Alkyne Metathesis; 22. Developments in Alkene Metathesis; 23. Developments in Alkene and Alkyne Metathesis; 24. Advances in Alkene and Alkyne Metathesis; 25. Developments in Alkene Metathesis; 26. Alkene Metathesis: Synthesis of Kainic Acid, Pladienolide B and Amphidinolide Y; 27. Alkene and Alkyne Metathesis: Phaseolinic Acid (Selvakumar), Methyl 7-Dihydro-trioxacarcinoside B (Koert), Arglabin (Reiser) and Amphidinolide V (Fürstner) 28. Alkene Metathesis: Synthesis of Panaxytriol (Lee), Isofagomine (Imahori and Takahata), Elatol (Stoltz), 5-F[Sub(2t)]-Isoprostane (Snapper), and Ottelione B (Clive)29. Total Synthesis by Alkene Metathesis: Amphidinolide X (Urpí/Vilarrasa), Dactylolide (Jennings), Cytotrienin A (Hayashi), Lepadin B (Charette), Blumiolide C (Altmann); Enantioselective Construction of Acyclic Stereogenic Centers; 30. Enantioselective Assembly of Oxygenated Stereogenic Centers; 31. Enantioselective Assembly of Aminated Stereogenic Centers; 32. Enantioselective Preparation of Secondary Alcohols and Amines 33. Enantioselective Preparation of Alcohols and Amines34. Enantioselective Synthesis of Alcohols and Amines; 35. Enantioselective Assembly of Alkylated Stereogenic Centers; 36. Enantioselective Construction of Alkylated Stereogenic Centers; 37. Enantioselective Construction of Alkylated Centers; 38. Enantioselective Construction of Alkylated Stereogenic Centers; 39. Stereocontrolled Construction of Arrays of Stereogenic Centers; 40. Enantioselective Construction of Arrays of Stereogenic Centers; 41. Stereocontrolled Construction of Arrays of Stereogenic Centers 42. Practical Enantioselective Construction of Arrays of Stereogenic Centers: The Jørgensen Synthesis of the Autoregulator IM-2 |
| Record Nr. | UNINA-9910461356803321 |
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Taber D. F (Douglass F.), <1948->
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| Oxford ; ; New York, : Oxford University Press, 2011 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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