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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 : a practical guide to over 750 transformations / / A. Hassner, I. Namboothiri
| Organic syntheses based on name reactions : 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 | ||
| ||