Info
- Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.
Carbonyl compounds : reactants, catalysts and products / / Feng Shi, Hongli Wang, Xingchao Dai
| Carbonyl compounds : reactants, catalysts and products / / Feng Shi, Hongli Wang, Xingchao Dai |
| Autore | Shi Feng |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH, , [2022] |
| Descrizione fisica | 1 online resource (375 pages) |
| Disciplina | 547.036 |
| Soggetto topico | Carbonyl compounds |
| Soggetto genere / forma | Electronic books. |
| ISBN |
3-527-82561-4
3-527-82562-2 3-527-82560-6 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Title Page -- Copyright -- Contents -- Preface -- Part I Carbonyl Molecules as Reactants -- Chapter 1 Carbon Monoxide -- 1.1 Hydroformylation of Alkenes and Alkynes -- 1.1.1 Co Catalysts -- 1.1.2 Rh Catalysts -- 1.1.3 Au Catalysts -- 1.1.4 Ligand‐Modified Heterogeneous Catalysts -- 1.1.5 Single‐Atom Catalysts -- 1.2 Hydroxy-, Alkoxy-, and Aminocarbonylation of Alkenes and Alkynes -- 1.2.1 Hydroxycarbonylation of Alkenes -- 1.2.2 Hydroxycarbonylation of Alkynes -- 1.2.3 Alkoxycarbonylation of Alkenes -- 1.2.4 Alkoxycarbonylation of Alkynes -- 1.2.5 Aminocarbonylation of Alkenes -- 1.2.6 Aminocarbonylation of Alkynes -- 1.3 The Pauson-Khand Reaction -- 1.3.1 The Catalytic Pauson-Khand Reaction -- 1.3.2 Stereoselective Pauson-Khand Reactions -- 1.3.3 Pauson-Khand Transfer Carbonylation Reactions -- 1.4 Synthesis of Acetic Acid -- 1.4.1 Process Considerations -- 1.4.2 Rhodium‐Catalyzed Carbonylation -- 1.4.3 Iridium‐Catalyzed Carbonylation -- 1.5 Carbonylation of C X Bonds -- 1.5.1 Hydroxy‐, Alkoxy‐, and Aminocarbonylations of C X Bonds -- 1.5.2 Reductive Carbonylations -- 1.5.3 Carbonylative Coupling Reactions with Organometallic Reagents -- 1.5.4 Carbonylative Sonogashira Reactions -- 1.5.5 Carbonylative C-H Activation Reactions -- 1.5.6 Carbonylative Heck Reactions -- 1.6 Carbonylation of Epoxides -- 1.6.1 Ring‐expansion Carbonylation of Epoxides -- 1.6.2 Hydroformylation and Silylformylation of Epoxides -- 1.6.3 Alternating Copolymerization of Epoxides -- 1.6.4 Alkoxycarbonylation and Aminocarbonylation of Epoxides -- 1.7 Carbonylation of Aldehydes -- 1.7.1 Amidocarbonylations of Aldehydes -- 1.7.2 Hydroformylation and Silylformylation of Aldehydes -- 1.7.3 Hetero Pauson-Khand Reactions of Aldehydes -- 1.7.4 Reactions of Aldehydes with Acylanions -- 1.7.5 Miscellaneous of Aldehydes -- 1.8 Oxidative Carbonylation Reaction.
1.8.1 Oxidative Carbonylation of Alkenes -- 1.8.2 Oxidative Carbonylation of Alkynes -- 1.8.3 Oxidative Carbonylation of Organometallic Reagents -- 1.8.4 Oxidative Carbonylation of Arenes -- 1.8.5 Oxidative Carbonylation of Amines -- 1.9 Other Reactions -- 1.9.1 Reactions of Diazoalkanes with Carbon Monoxide -- 1.9.2 Reaction of C-NO2 with CO -- Chapter 2 Carbon Dioxide -- 2.1 Synthesis of Urea Derivatives -- 2.1.1 Metal‐free Catalyst Systems -- 2.1.2 Ph3SbO as Catalyst -- 2.1.3 Pd Catalyst Systems -- 2.1.4 Ionic Liquids as Catalyst -- 2.1.5 CeO2 as Catalyst -- 2.2 Synthesis of Carbamate Derivatives -- 2.2.1 Ru Catalyst Systems -- 2.2.2 Sn or Ni Catalyst Systems -- 2.2.3 Zeolite as Catalyst -- 2.2.4 Other Catalyst Systems -- 2.3 Synthesis of Carboxyl Acid Derivatives -- 2.4 Cycloaddition of Epoxide with CO2 -- 2.4.1 Oxides Catalysts -- 2.4.2 Zeolite Catalysts -- 2.4.3 Supported Nanoparticle and Lewis Acid Catalysts -- 2.4.4 Carbon Catalysts -- 2.4.5 Salen, Porphyrins, and Phthalocyanines Catalysts -- 2.4.6 Ionic Liquid Catalysts -- 2.4.7 Metal-Organic Framework (MOF) Catalysts -- 2.4.8 Bifunctional Catalysts -- 2.4.9 Other Catalysts -- 2.5 Reaction of Polyalcohols/Olefins with CO2 -- 2.6 Formylation of Amines with CO2 -- 2.7 Reactions of Propargyl Alcohols/Propargyl Amines with CO2 -- 2.8 Other Reactions -- 2.8.1 Reactions of Aromatic Halides with CO2 -- 2.8.2 Reactions of 2‐Aminobenzonitriles with CO2 -- Chapter 3 Other C1 Carbonyl Molecules -- 3.1 Formaldehyde (HCHO) -- 3.1.1 Carbonylation of Halides with HCHO -- 3.1.2 Carbonylation of Olefins with HCHO -- 3.1.3 Carbonylation of Alkynes with HCHO -- 3.2 Formic Acid (HCOOH) -- 3.2.1 Hydroxycarbonylation of Arenes with Formic Acid -- 3.2.2 Carbonylation of Alkenes with Formic Acid -- 3.2.3 Carbonylation of Alkynes with Formic Acid -- 3.2.4 N‐Formylation Reactions with Formic Acid. 3.2.4.1 Metal Oxides Catalysts -- 3.2.4.2 Brønsted Acidic as Catalyst -- 3.2.4.3 Amberlite IR‐120 Resins as Catalysts -- 3.2.4.4 Magnetic Catalysts -- 3.2.4.5 Zeolite as Catalyst -- 3.2.4.6 Ionic Liquids (ILs) as Catalyst -- 3.2.4.7 Other Catalysts -- 3.2.5 Carbonylation of C-X with Formic Acid -- 3.2.6 Other Reactions -- Chapter 4 CO Surrogates -- 4.1 Carbonyl Metal -- 4.2 Formates -- 4.3 Formamides -- 4.4 Formic Anhydride -- 4.5 Silacarboxylic Acid -- 4.6 N‐Formylsaccharin -- 4.7 Acyl Chloride -- 4.8 In Situ Generated Carbonyl Source -- 4.8.1 Methanol -- 4.8.2 Glycerol -- 4.8.3 Aldoses -- 4.8.4 Epoxide -- 4.8.5 Chloroform -- 4.8.5.1 Pd‐catalyzed Carbonylation Reactions -- 4.8.5.2 Fe‐Catalyzed Carbonylation Reactions -- 4.8.5.3 Zn‐Catalyzed Carbonylation Reactions -- Part I References -- Part II Carbonyl Compounds as Catalysts -- Chapter 5 Acid‐Catalyzed Reactions with -CO2H -- 5.1 Carboxylic Acid Molecules Catalyzed Reactions -- 5.1.1 Hydrolysis/Aminolysis/Ethanolysis Reactions -- 5.1.2 Mutarotation of 2,3,4,6‐Tetramethyl‐d‐glucose (TM‐G) -- 5.1.3 Depolymerization of Polyoxymethylenes -- 5.1.4 Elimination Reactions -- 5.1.5 Hydrogen-Deuterium Exchange Reactions -- 5.1.6 Reduction Reactions -- 5.1.7 Decomposition of Diazodiphenylmethane -- 5.1.8 Amino-Imino Tautomerism Reactions -- 5.1.9 Aldol Reaction -- 5.1.10 Friedel-Crafts Reaction -- 5.1.11 Hydrogen Shifts Reaction -- 5.1.12 Cyclization Reaction -- 5.1.13 Hydroboration Reaction -- 5.1.14 Trifluoromethylation Reaction -- 5.2 Carbon Material-Catalyzed Reactions -- 5.2.1 Reduction of Nitric Oxide -- 5.2.2 Oxidative Coupling of Amines to Imines -- 5.2.3 Depolymerization of Cellulose and Lignocellulose -- 5.2.4 Nitrobenzene Reduction Reaction and Beckmann Rearrangement Reaction -- 5.2.5 Ring‐Opening Reaction of Styrene Oxide -- Chapter 6 Reactions via Carbonyl and Hydroxyl Groups Recycling. 6.1 Carbon‐Catalyzed Selective Oxidation Reactions -- 6.1.1 Oxidative Dehydrogenation of Ethylbenzene -- 6.1.2 Oxidative Dehydrogenation of n‐Butane -- 6.1.3 Oxidative Dehydrogenation of Isobutane -- 6.1.4 Oxidative Dehydrogenation of Propane -- 6.2 Polymer‐Catalyzed Selective Oxidation Reactions -- 6.2.1 Oxidative Dehydrogenation of Ethylbenzene -- 6.2.2 Oxidative Dehydrogenation of Heterocyclic Compounds -- 6.3 Aldehyde/Ketone‐Catalyzed Borrowing‐Hydrogen Reactions -- 6.3.1 Dehydrative β‐C‐Alkylation Reaction of Methyl Carbinols with Alcohols -- 6.3.2 Dehydrative α‐Alkylation Reactions of Ketones with Alcohols -- 6.3.3 Dehydrative Alkylation Reactions of Fluorenes with Alcohols -- 6.3.4 Dehydrative N‐Alkylation Reactions of Amines with Alcohols -- 6.4 Carbon‐Catalyzed Borrowing‐Hydrogen Reactions -- Part II References -- Part III The Synthetic Applications of Carbonyl Compounds -- Chapter 7 Synthesis of Functional Molecules -- 7.1 Reduction of Carbonyl Compounds -- 7.1.1 Aldehydes and Ketones to Alcohol -- 7.1.2 Acids to the Alcohols and Aldehydes -- 7.1.2.1 To Alcohols -- 7.1.2.2 To Aldehydes -- 7.1.3 Ester to Alcohols and Ethers -- 7.1.3.1 To Alcohols -- 7.1.3.2 To Ethers -- 7.1.4 Amides to Amines -- 7.1.5 Clemmensen Reduction -- 7.1.6 Wolff-Kishner Reduction -- 7.2 Nucleophilic Addition Reactions of Aldehydes and Ketones -- 7.2.1 Carbon Nucleophiles -- 7.2.1.1 Grignard Reagent and Other Organometallic Reagents -- 7.2.1.2 Reformatsky Reaction -- 7.2.1.3 Benzoin Condensation -- 7.2.1.4 CN Group -- 7.2.1.5 Aromatic and Aliphatic C H Bond -- 7.2.2 Nitrogen Nucleophiles -- 7.2.3 Oxygen Nucleophiles -- 7.2.3.1 H2O as a Nucleophile -- 7.2.3.2 ROH as a Nucleophile -- 7.3 Addition Elimination Reactions of Aldehydes and Ketones -- 7.3.1 Aldol Reaction -- 7.3.2 Perkin Reaction -- 7.3.3 Knoevenagel Condensation -- 7.4 Oxidation of Aldehydes and Ketones. 7.4.1 Baeyer-Villiger Oxidation -- 7.4.2 To Acid -- 7.5 Wittig Reaction -- 7.6 Reductive Amination Reaction -- 7.6.1 Homogeneous Catalyst System -- 7.6.2 Heterogeneous Catalyst System -- 7.7 Hydroboration/Hydrophosphonylation/Hydrosilylation/Hydroacylation of Aldehydes and Ketones -- 7.7.1 Hydroboration -- 7.7.2 Hydrophosphonylation -- 7.7.3 Hydrosilylation Reactions -- 7.7.4 Hydroacylation Reactions -- 7.8 Oxidative Cross‐Coupling Reaction of Aldehydes -- 7.8.1 Homogeneous Catalyst System -- 7.8.2 Heterogeneous Catalyst System -- 7.9 Reductive Coupling Reactions of Aldehydes -- 7.10 Reaction of Acids as Starting Materials -- 7.10.1 Esterification Reactions -- 7.10.2 Amidation Reactions -- 7.10.3 Decarboxylation Coupling Reactions -- 7.11 Reaction of Esters as Starting Materials -- 7.11.1 Hydrolysis Reaction -- 7.11.2 Transesterification Reaction -- 7.11.3 Aminolysis Reaction -- 7.12 Reaction of Amides as Starting Materials -- 7.12.1 Hydrolysis Reaction -- 7.12.2 Alcoholysis Reaction -- Chapter 8 Synthesis of Functional Materials -- 8.1 Polyamides -- 8.1.1 Aliphatic Polyamides -- 8.1.2 Aromatic Polyamides -- 8.1.3 Long‐Chain Semiaromatic Polyamides -- 8.2 Phenol Formaldehyde Resins -- 8.2.1 Novolac Resins -- 8.2.2 Resole Resins -- 8.3 Polyurethanes -- 8.4 Polyesters -- Part III References -- Chapter 9 Conclusion and Perspectives -- 9.1 Conclusion -- 9.2 Perspectives -- Index -- EULA. |
| Record Nr. | UNINA-9910555179403321 |
Shi Feng
|
||
| Weinheim, Germany : , : Wiley-VCH, , [2022] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Carbonyl compounds : reactants, catalysts and products / / Feng Shi, Hongli Wang, Xingchao Dai
| Carbonyl compounds : reactants, catalysts and products / / Feng Shi, Hongli Wang, Xingchao Dai |
| Autore | Shi Feng |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH, , [2022] |
| Descrizione fisica | 1 online resource (375 pages) |
| Disciplina | 547.036 |
| Soggetto topico | Carbonyl compounds |
| ISBN |
3-527-82561-4
3-527-82562-2 3-527-82560-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Title Page -- Copyright -- Contents -- Preface -- Part I Carbonyl Molecules as Reactants -- Chapter 1 Carbon Monoxide -- 1.1 Hydroformylation of Alkenes and Alkynes -- 1.1.1 Co Catalysts -- 1.1.2 Rh Catalysts -- 1.1.3 Au Catalysts -- 1.1.4 Ligand‐Modified Heterogeneous Catalysts -- 1.1.5 Single‐Atom Catalysts -- 1.2 Hydroxy-, Alkoxy-, and Aminocarbonylation of Alkenes and Alkynes -- 1.2.1 Hydroxycarbonylation of Alkenes -- 1.2.2 Hydroxycarbonylation of Alkynes -- 1.2.3 Alkoxycarbonylation of Alkenes -- 1.2.4 Alkoxycarbonylation of Alkynes -- 1.2.5 Aminocarbonylation of Alkenes -- 1.2.6 Aminocarbonylation of Alkynes -- 1.3 The Pauson-Khand Reaction -- 1.3.1 The Catalytic Pauson-Khand Reaction -- 1.3.2 Stereoselective Pauson-Khand Reactions -- 1.3.3 Pauson-Khand Transfer Carbonylation Reactions -- 1.4 Synthesis of Acetic Acid -- 1.4.1 Process Considerations -- 1.4.2 Rhodium‐Catalyzed Carbonylation -- 1.4.3 Iridium‐Catalyzed Carbonylation -- 1.5 Carbonylation of C X Bonds -- 1.5.1 Hydroxy‐, Alkoxy‐, and Aminocarbonylations of C X Bonds -- 1.5.2 Reductive Carbonylations -- 1.5.3 Carbonylative Coupling Reactions with Organometallic Reagents -- 1.5.4 Carbonylative Sonogashira Reactions -- 1.5.5 Carbonylative C-H Activation Reactions -- 1.5.6 Carbonylative Heck Reactions -- 1.6 Carbonylation of Epoxides -- 1.6.1 Ring‐expansion Carbonylation of Epoxides -- 1.6.2 Hydroformylation and Silylformylation of Epoxides -- 1.6.3 Alternating Copolymerization of Epoxides -- 1.6.4 Alkoxycarbonylation and Aminocarbonylation of Epoxides -- 1.7 Carbonylation of Aldehydes -- 1.7.1 Amidocarbonylations of Aldehydes -- 1.7.2 Hydroformylation and Silylformylation of Aldehydes -- 1.7.3 Hetero Pauson-Khand Reactions of Aldehydes -- 1.7.4 Reactions of Aldehydes with Acylanions -- 1.7.5 Miscellaneous of Aldehydes -- 1.8 Oxidative Carbonylation Reaction.
1.8.1 Oxidative Carbonylation of Alkenes -- 1.8.2 Oxidative Carbonylation of Alkynes -- 1.8.3 Oxidative Carbonylation of Organometallic Reagents -- 1.8.4 Oxidative Carbonylation of Arenes -- 1.8.5 Oxidative Carbonylation of Amines -- 1.9 Other Reactions -- 1.9.1 Reactions of Diazoalkanes with Carbon Monoxide -- 1.9.2 Reaction of C-NO2 with CO -- Chapter 2 Carbon Dioxide -- 2.1 Synthesis of Urea Derivatives -- 2.1.1 Metal‐free Catalyst Systems -- 2.1.2 Ph3SbO as Catalyst -- 2.1.3 Pd Catalyst Systems -- 2.1.4 Ionic Liquids as Catalyst -- 2.1.5 CeO2 as Catalyst -- 2.2 Synthesis of Carbamate Derivatives -- 2.2.1 Ru Catalyst Systems -- 2.2.2 Sn or Ni Catalyst Systems -- 2.2.3 Zeolite as Catalyst -- 2.2.4 Other Catalyst Systems -- 2.3 Synthesis of Carboxyl Acid Derivatives -- 2.4 Cycloaddition of Epoxide with CO2 -- 2.4.1 Oxides Catalysts -- 2.4.2 Zeolite Catalysts -- 2.4.3 Supported Nanoparticle and Lewis Acid Catalysts -- 2.4.4 Carbon Catalysts -- 2.4.5 Salen, Porphyrins, and Phthalocyanines Catalysts -- 2.4.6 Ionic Liquid Catalysts -- 2.4.7 Metal-Organic Framework (MOF) Catalysts -- 2.4.8 Bifunctional Catalysts -- 2.4.9 Other Catalysts -- 2.5 Reaction of Polyalcohols/Olefins with CO2 -- 2.6 Formylation of Amines with CO2 -- 2.7 Reactions of Propargyl Alcohols/Propargyl Amines with CO2 -- 2.8 Other Reactions -- 2.8.1 Reactions of Aromatic Halides with CO2 -- 2.8.2 Reactions of 2‐Aminobenzonitriles with CO2 -- Chapter 3 Other C1 Carbonyl Molecules -- 3.1 Formaldehyde (HCHO) -- 3.1.1 Carbonylation of Halides with HCHO -- 3.1.2 Carbonylation of Olefins with HCHO -- 3.1.3 Carbonylation of Alkynes with HCHO -- 3.2 Formic Acid (HCOOH) -- 3.2.1 Hydroxycarbonylation of Arenes with Formic Acid -- 3.2.2 Carbonylation of Alkenes with Formic Acid -- 3.2.3 Carbonylation of Alkynes with Formic Acid -- 3.2.4 N‐Formylation Reactions with Formic Acid. 3.2.4.1 Metal Oxides Catalysts -- 3.2.4.2 Brønsted Acidic as Catalyst -- 3.2.4.3 Amberlite IR‐120 Resins as Catalysts -- 3.2.4.4 Magnetic Catalysts -- 3.2.4.5 Zeolite as Catalyst -- 3.2.4.6 Ionic Liquids (ILs) as Catalyst -- 3.2.4.7 Other Catalysts -- 3.2.5 Carbonylation of C-X with Formic Acid -- 3.2.6 Other Reactions -- Chapter 4 CO Surrogates -- 4.1 Carbonyl Metal -- 4.2 Formates -- 4.3 Formamides -- 4.4 Formic Anhydride -- 4.5 Silacarboxylic Acid -- 4.6 N‐Formylsaccharin -- 4.7 Acyl Chloride -- 4.8 In Situ Generated Carbonyl Source -- 4.8.1 Methanol -- 4.8.2 Glycerol -- 4.8.3 Aldoses -- 4.8.4 Epoxide -- 4.8.5 Chloroform -- 4.8.5.1 Pd‐catalyzed Carbonylation Reactions -- 4.8.5.2 Fe‐Catalyzed Carbonylation Reactions -- 4.8.5.3 Zn‐Catalyzed Carbonylation Reactions -- Part I References -- Part II Carbonyl Compounds as Catalysts -- Chapter 5 Acid‐Catalyzed Reactions with -CO2H -- 5.1 Carboxylic Acid Molecules Catalyzed Reactions -- 5.1.1 Hydrolysis/Aminolysis/Ethanolysis Reactions -- 5.1.2 Mutarotation of 2,3,4,6‐Tetramethyl‐d‐glucose (TM‐G) -- 5.1.3 Depolymerization of Polyoxymethylenes -- 5.1.4 Elimination Reactions -- 5.1.5 Hydrogen-Deuterium Exchange Reactions -- 5.1.6 Reduction Reactions -- 5.1.7 Decomposition of Diazodiphenylmethane -- 5.1.8 Amino-Imino Tautomerism Reactions -- 5.1.9 Aldol Reaction -- 5.1.10 Friedel-Crafts Reaction -- 5.1.11 Hydrogen Shifts Reaction -- 5.1.12 Cyclization Reaction -- 5.1.13 Hydroboration Reaction -- 5.1.14 Trifluoromethylation Reaction -- 5.2 Carbon Material-Catalyzed Reactions -- 5.2.1 Reduction of Nitric Oxide -- 5.2.2 Oxidative Coupling of Amines to Imines -- 5.2.3 Depolymerization of Cellulose and Lignocellulose -- 5.2.4 Nitrobenzene Reduction Reaction and Beckmann Rearrangement Reaction -- 5.2.5 Ring‐Opening Reaction of Styrene Oxide -- Chapter 6 Reactions via Carbonyl and Hydroxyl Groups Recycling. 6.1 Carbon‐Catalyzed Selective Oxidation Reactions -- 6.1.1 Oxidative Dehydrogenation of Ethylbenzene -- 6.1.2 Oxidative Dehydrogenation of n‐Butane -- 6.1.3 Oxidative Dehydrogenation of Isobutane -- 6.1.4 Oxidative Dehydrogenation of Propane -- 6.2 Polymer‐Catalyzed Selective Oxidation Reactions -- 6.2.1 Oxidative Dehydrogenation of Ethylbenzene -- 6.2.2 Oxidative Dehydrogenation of Heterocyclic Compounds -- 6.3 Aldehyde/Ketone‐Catalyzed Borrowing‐Hydrogen Reactions -- 6.3.1 Dehydrative β‐C‐Alkylation Reaction of Methyl Carbinols with Alcohols -- 6.3.2 Dehydrative α‐Alkylation Reactions of Ketones with Alcohols -- 6.3.3 Dehydrative Alkylation Reactions of Fluorenes with Alcohols -- 6.3.4 Dehydrative N‐Alkylation Reactions of Amines with Alcohols -- 6.4 Carbon‐Catalyzed Borrowing‐Hydrogen Reactions -- Part II References -- Part III The Synthetic Applications of Carbonyl Compounds -- Chapter 7 Synthesis of Functional Molecules -- 7.1 Reduction of Carbonyl Compounds -- 7.1.1 Aldehydes and Ketones to Alcohol -- 7.1.2 Acids to the Alcohols and Aldehydes -- 7.1.2.1 To Alcohols -- 7.1.2.2 To Aldehydes -- 7.1.3 Ester to Alcohols and Ethers -- 7.1.3.1 To Alcohols -- 7.1.3.2 To Ethers -- 7.1.4 Amides to Amines -- 7.1.5 Clemmensen Reduction -- 7.1.6 Wolff-Kishner Reduction -- 7.2 Nucleophilic Addition Reactions of Aldehydes and Ketones -- 7.2.1 Carbon Nucleophiles -- 7.2.1.1 Grignard Reagent and Other Organometallic Reagents -- 7.2.1.2 Reformatsky Reaction -- 7.2.1.3 Benzoin Condensation -- 7.2.1.4 CN Group -- 7.2.1.5 Aromatic and Aliphatic C H Bond -- 7.2.2 Nitrogen Nucleophiles -- 7.2.3 Oxygen Nucleophiles -- 7.2.3.1 H2O as a Nucleophile -- 7.2.3.2 ROH as a Nucleophile -- 7.3 Addition Elimination Reactions of Aldehydes and Ketones -- 7.3.1 Aldol Reaction -- 7.3.2 Perkin Reaction -- 7.3.3 Knoevenagel Condensation -- 7.4 Oxidation of Aldehydes and Ketones. 7.4.1 Baeyer-Villiger Oxidation -- 7.4.2 To Acid -- 7.5 Wittig Reaction -- 7.6 Reductive Amination Reaction -- 7.6.1 Homogeneous Catalyst System -- 7.6.2 Heterogeneous Catalyst System -- 7.7 Hydroboration/Hydrophosphonylation/Hydrosilylation/Hydroacylation of Aldehydes and Ketones -- 7.7.1 Hydroboration -- 7.7.2 Hydrophosphonylation -- 7.7.3 Hydrosilylation Reactions -- 7.7.4 Hydroacylation Reactions -- 7.8 Oxidative Cross‐Coupling Reaction of Aldehydes -- 7.8.1 Homogeneous Catalyst System -- 7.8.2 Heterogeneous Catalyst System -- 7.9 Reductive Coupling Reactions of Aldehydes -- 7.10 Reaction of Acids as Starting Materials -- 7.10.1 Esterification Reactions -- 7.10.2 Amidation Reactions -- 7.10.3 Decarboxylation Coupling Reactions -- 7.11 Reaction of Esters as Starting Materials -- 7.11.1 Hydrolysis Reaction -- 7.11.2 Transesterification Reaction -- 7.11.3 Aminolysis Reaction -- 7.12 Reaction of Amides as Starting Materials -- 7.12.1 Hydrolysis Reaction -- 7.12.2 Alcoholysis Reaction -- Chapter 8 Synthesis of Functional Materials -- 8.1 Polyamides -- 8.1.1 Aliphatic Polyamides -- 8.1.2 Aromatic Polyamides -- 8.1.3 Long‐Chain Semiaromatic Polyamides -- 8.2 Phenol Formaldehyde Resins -- 8.2.1 Novolac Resins -- 8.2.2 Resole Resins -- 8.3 Polyurethanes -- 8.4 Polyesters -- Part III References -- Chapter 9 Conclusion and Perspectives -- 9.1 Conclusion -- 9.2 Perspectives -- Index -- EULA. |
| Record Nr. | UNINA-9910830037203321 |
|
Shi Feng
|
||
| Weinheim, Germany : , : Wiley-VCH, , [2022] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chemistry characterization of jet aircraft engine particulate by XPS : results from APEX III / / Randy L. Vander Wal, Victoria M. Bryg
| Chemistry characterization of jet aircraft engine particulate by XPS : results from APEX III / / Randy L. Vander Wal, Victoria M. Bryg |
| Autore | Vander Wal R (Randy L.) |
| Pubbl/distr/stampa | Cleveland, Ohio : , : National Aeronautics and Space Administration, Glenn Research Center, , June 2014 |
| Descrizione fisica | 1 online resource (9 pages) : illustrations |
| Collana | NASA/CR |
| Soggetto topico |
Jet exhaust
Exhaust emission Carboxylic acids Carbonyl compounds Photoelectron spectroscopy X ray spectroscopy |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Chemistry characterization of jet aircraft engine particulate by XPS |
| Record Nr. | UNINA-9910702720803321 |
|
Vander Wal R (Randy L.)
|
||
| Cleveland, Ohio : , : National Aeronautics and Space Administration, Glenn Research Center, , June 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
The Chemistry of Carbonyl Group
| The Chemistry of Carbonyl Group |
| Autore | Patai Saul E |
| Pubbl/distr/stampa | [Place of publication not identified], : John Wiley & Sons Incorporated, 1966 |
| Descrizione fisica | 1 online resource |
| Disciplina | 547.43 |
| Collana | Chemistry of functional groups |
| Soggetto topico | Carbonyl compounds |
| ISBN |
0-470-77820-2
0-470-77105-4 0-470-77113-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | v. 1. General and theoretical aspects of the carbonyl group -- G. Berthier and J. Serre -- Carbonyl-forming oxidations -- C.F. Cullis and A. Fish -- Formation of carbonyl groups in hydrolytic reactions -- Pentti Salomaa -- Formation of aldehydes and ketones from carboxylic acids and their derivatives -- Reynold. C. Fuson -- Formation of ketones and aldehydes by acylation, formylation and some related processes -- D.P.N. Satchell and R.S. Satchell -- Carbonyl syntheses through organometallics -- Michael Cais and Asher Mandelbaum -- Biological formation and reactions of carbonyl groups -- Frank Eisenberg -- Chemical and physical methods of analysis -- J. Gordon Hanna -- Basicity of carbonyl compounds -- V.A. Palm, Ü.L. Haldna and A.J. Talvik -- Oxidation of aldehydes by transition metals -- Jan Roček -- Reduction of carbonyl groups -- Owen H. Wheeler -- Condensations leading to double bonds -- Richard L. Reeves -- Reactions of carbonyl groups with organometallic compounds -- Theophil Eicher -- Decarbonylation -- W.M. Schubert and Robert Roy Kintner -- Rearrangements involving the carbonyl group -- Clair J. Collins and Jerome F. Eastham -- Photochemistry of ketones and aldehydes - J.N. Pitts and J.K.S. Wan -- Thioketones -- E. Campaigne -- v. 2. Equilibrium additions to carbonyl compounds -- Yoshiro Ogata and Atsushi Kawasaki -- Oxidation of aldehydes and ketones -- Herbert S. Verter -- Enolization -- S. Forsén and M. Nilsson -- Oxocarbons and their reactions -- Robert West and Joseph Niu -- Mass spectrometry of carbonyl compounds -- J.H. Bowie -- Radiation chemistry of ketones and aldehydes -- Gordon R. Freeman. |
| Record Nr. | UNINA-9910830029503321 |
|
Patai Saul E
|
||
| [Place of publication not identified], : John Wiley & Sons Incorporated, 1966 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
The Chemistry of Carbonyl Group
| The Chemistry of Carbonyl Group |
| Autore | Patai Saul E |
| Pubbl/distr/stampa | [Place of publication not identified], : John Wiley & Sons Incorporated, 1966 |
| Descrizione fisica | 1 online resource |
| Disciplina | 547.43 |
| Collana | Chemistry of functional groups |
| Soggetto topico | Carbonyl compounds |
| ISBN |
0-470-77820-2
0-470-77105-4 0-470-77113-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | v. 1. General and theoretical aspects of the carbonyl group -- G. Berthier and J. Serre -- Carbonyl-forming oxidations -- C.F. Cullis and A. Fish -- Formation of carbonyl groups in hydrolytic reactions -- Pentti Salomaa -- Formation of aldehydes and ketones from carboxylic acids and their derivatives -- Reynold. C. Fuson -- Formation of ketones and aldehydes by acylation, formylation and some related processes -- D.P.N. Satchell and R.S. Satchell -- Carbonyl syntheses through organometallics -- Michael Cais and Asher Mandelbaum -- Biological formation and reactions of carbonyl groups -- Frank Eisenberg -- Chemical and physical methods of analysis -- J. Gordon Hanna -- Basicity of carbonyl compounds -- V.A. Palm, Ü.L. Haldna and A.J. Talvik -- Oxidation of aldehydes by transition metals -- Jan Roček -- Reduction of carbonyl groups -- Owen H. Wheeler -- Condensations leading to double bonds -- Richard L. Reeves -- Reactions of carbonyl groups with organometallic compounds -- Theophil Eicher -- Decarbonylation -- W.M. Schubert and Robert Roy Kintner -- Rearrangements involving the carbonyl group -- Clair J. Collins and Jerome F. Eastham -- Photochemistry of ketones and aldehydes - J.N. Pitts and J.K.S. Wan -- Thioketones -- E. Campaigne -- v. 2. Equilibrium additions to carbonyl compounds -- Yoshiro Ogata and Atsushi Kawasaki -- Oxidation of aldehydes and ketones -- Herbert S. Verter -- Enolization -- S. Forsén and M. Nilsson -- Oxocarbons and their reactions -- Robert West and Joseph Niu -- Mass spectrometry of carbonyl compounds -- J.H. Bowie -- Radiation chemistry of ketones and aldehydes -- Gordon R. Freeman. |
| Record Nr. | UNINA-9910841636203321 |
|
Patai Saul E
|
||
| [Place of publication not identified], : John Wiley & Sons Incorporated, 1966 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chemistry of Enones and Related Compounds
| Chemistry of Enones and Related Compounds |
| Autore | Patai Saul E |
| Pubbl/distr/stampa | [Place of publication not identified], : John Wiley & Sons Incorporated, 1989 |
| Descrizione fisica | 1 online resource (xvi, 1267 pages) : illustrations |
| Disciplina | 547.036 |
| Collana | PATAI'S Chemistry of Functional Groups |
| Soggetto topico | Carbonyl compounds |
| ISBN |
0-470-77883-0
0-470-77221-2 0-470-77232-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | [pt. 1.] General and theoretical / A.Y. Meyer -- Structural chemistry of enones / B. Schweizer -- Conformations, chiroptical and related spectral properties of enones / J. Gawronksi -- Thermochemistry of enones and related species / J.F. Liebman and R.M. Pollack -- NMR spectroscopy of enones / H.E. Gottlieb -- The chemistry of ionized enones in the gas phase / F. Tureček -- Synthesis of enones / C. Thebtaranonth and Y. Thebtaranonth -- Synthetic uses of enones / G.V. Boyd -- Acid-base behaviour of enones / R.I. Zalewski -- Nucleophilic attacks on enones / D. Duval and S. Géribaldi -- Additions of electrons or radicals to [alpha], [beta]-unsaturated enones / G.A. Russell -- The reaction of enones with electrophiles / K. Müllen and P. Wolf -- Chemical and enzymatic conversion of [beta], [gamma]-enomes to [alpha], [beta]-enones / R.M. Pollack, P.L. Bounds and C.L. Bevins -- [pt. 2.] Enone electrochemistry / R.D. Little and M.M. Baizer -- The photochemistry of enones / D.I. Schuster -- Radiation chemistry of enones / P. Neta and M. Dizdaroglu -- The oxygenation of enones / A.A. Frimer -- The reduction of [alpha], [beta]-unsaturated carbonyl compounds / E. Keinan and N. Greenspoon -- Organometallic derivatives of [alpha], [beta]-unsaturated enones / J.A.S. Howell -- Dienols (enolization of enones) / B. Capon -- Asymmetric synthesis with chiral enones / M.R. Peel and C.R. Johnson -- Dimerization and polymerization of enones in the fluid and solid states / C.R. Theocharis. |
| Record Nr. | UNINA-9910830853203321 |
|
Patai Saul E
|
||
| [Place of publication not identified], : John Wiley & Sons Incorporated, 1989 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chemistry of Enones and Related Compounds
| Chemistry of Enones and Related Compounds |
| Autore | Patai Saul E |
| Pubbl/distr/stampa | [Place of publication not identified], : John Wiley & Sons Incorporated, 1989 |
| Descrizione fisica | 1 online resource (xvi, 1267 pages) : illustrations |
| Disciplina | 547.036 |
| Collana | PATAI'S Chemistry of Functional Groups |
| Soggetto topico | Carbonyl compounds |
| ISBN |
0-470-77883-0
0-470-77221-2 0-470-77232-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | [pt. 1.] General and theoretical / A.Y. Meyer -- Structural chemistry of enones / B. Schweizer -- Conformations, chiroptical and related spectral properties of enones / J. Gawronksi -- Thermochemistry of enones and related species / J.F. Liebman and R.M. Pollack -- NMR spectroscopy of enones / H.E. Gottlieb -- The chemistry of ionized enones in the gas phase / F. Tureček -- Synthesis of enones / C. Thebtaranonth and Y. Thebtaranonth -- Synthetic uses of enones / G.V. Boyd -- Acid-base behaviour of enones / R.I. Zalewski -- Nucleophilic attacks on enones / D. Duval and S. Géribaldi -- Additions of electrons or radicals to [alpha], [beta]-unsaturated enones / G.A. Russell -- The reaction of enones with electrophiles / K. Müllen and P. Wolf -- Chemical and enzymatic conversion of [beta], [gamma]-enomes to [alpha], [beta]-enones / R.M. Pollack, P.L. Bounds and C.L. Bevins -- [pt. 2.] Enone electrochemistry / R.D. Little and M.M. Baizer -- The photochemistry of enones / D.I. Schuster -- Radiation chemistry of enones / P. Neta and M. Dizdaroglu -- The oxygenation of enones / A.A. Frimer -- The reduction of [alpha], [beta]-unsaturated carbonyl compounds / E. Keinan and N. Greenspoon -- Organometallic derivatives of [alpha], [beta]-unsaturated enones / J.A.S. Howell -- Dienols (enolization of enones) / B. Capon -- Asymmetric synthesis with chiral enones / M.R. Peel and C.R. Johnson -- Dimerization and polymerization of enones in the fluid and solid states / C.R. Theocharis. |
| Record Nr. | UNINA-9910841157803321 |
|
Patai Saul E
|
||
| [Place of publication not identified], : John Wiley & Sons Incorporated, 1989 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
The Chemistry of Enones. Vol. 2
| The Chemistry of Enones. Vol. 2 |
| Autore | Patai Saul E |
| Pubbl/distr/stampa | [Place of publication not identified], : John Wiley & Sons Incorporated, 1989 |
| Descrizione fisica | 1 online resource (xvi, 1267 pages) : illustrations |
| Disciplina | 547.036 |
| Collana | PATAI'S Chemistry of Functional Groups |
| Soggetto topico |
Carbonyl compounds
Functional groups |
| ISBN |
0-470-77884-9
0-470-77222-0 0-470-77233-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | [pt. 1.] General and theoretical / A.Y. Meyer -- Structural chemistry of enones / B. Schweizer -- Conformations, chiroptical and related spectral properties of enones / J. Gawronksi -- Thermochemistry of enones and related species / J.F. Liebman and R.M. Pollack -- NMR spectroscopy of enones / H.E. Gottlieb -- The chemistry of ionized enones in the gas phase / F. Tureček -- Synthesis of enones / C. Thebtaranonth and Y. Thebtaranonth -- Synthetic uses of enones / G.V. Boyd -- Acid-base behaviour of enones / R.I. Zalewski -- Nucleophilic attacks on enones / D. Duval and S. Géribaldi -- Additions of electrons or radicals to [alpha], [beta]-unsaturated enones / G.A. Russell -- The reaction of enones with electrophiles / K. Müllen and P. Wolf -- Chemical and enzymatic conversion of [beta], [gamma]-enomes to [alpha], [beta]-enones / R.M. Pollack, P.L. Bounds and C.L. Bevins -- [pt. 2.] Enone electrochemistry / R.D. Little and M.M. Baizer -- The photochemistry of enones / D.I. Schuster -- Radiation chemistry of enones / P. Neta and M. Dizdaroglu -- The oxygenation of enones / A.A. Frimer -- The reduction of [alpha], [beta]-unsaturated carbonyl compounds / E. Keinan and N. Greenspoon -- Organometallic derivatives of [alpha], [beta]-unsaturated enones / J.A.S. Howell -- Dienols (enolization of enones) / B. Capon -- Asymmetric synthesis with chiral enones / M.R. Peel and C.R. Johnson -- Dimerization and polymerization of enones in the fluid and solid states / C.R. Theocharis. |
| Record Nr. | UNINA-9910829971303321 |
|
Patai Saul E
|
||
| [Place of publication not identified], : John Wiley & Sons Incorporated, 1989 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
The Chemistry of Enones. Vol. 2
| The Chemistry of Enones. Vol. 2 |
| Autore | Patai Saul E |
| Pubbl/distr/stampa | [Place of publication not identified], : John Wiley & Sons Incorporated, 1989 |
| Descrizione fisica | 1 online resource (xvi, 1267 pages) : illustrations |
| Disciplina | 547.036 |
| Collana | PATAI'S Chemistry of Functional Groups |
| Soggetto topico |
Carbonyl compounds
Functional groups |
| ISBN |
0-470-77884-9
0-470-77222-0 0-470-77233-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | [pt. 1.] General and theoretical / A.Y. Meyer -- Structural chemistry of enones / B. Schweizer -- Conformations, chiroptical and related spectral properties of enones / J. Gawronksi -- Thermochemistry of enones and related species / J.F. Liebman and R.M. Pollack -- NMR spectroscopy of enones / H.E. Gottlieb -- The chemistry of ionized enones in the gas phase / F. Tureček -- Synthesis of enones / C. Thebtaranonth and Y. Thebtaranonth -- Synthetic uses of enones / G.V. Boyd -- Acid-base behaviour of enones / R.I. Zalewski -- Nucleophilic attacks on enones / D. Duval and S. Géribaldi -- Additions of electrons or radicals to [alpha], [beta]-unsaturated enones / G.A. Russell -- The reaction of enones with electrophiles / K. Müllen and P. Wolf -- Chemical and enzymatic conversion of [beta], [gamma]-enomes to [alpha], [beta]-enones / R.M. Pollack, P.L. Bounds and C.L. Bevins -- [pt. 2.] Enone electrochemistry / R.D. Little and M.M. Baizer -- The photochemistry of enones / D.I. Schuster -- Radiation chemistry of enones / P. Neta and M. Dizdaroglu -- The oxygenation of enones / A.A. Frimer -- The reduction of [alpha], [beta]-unsaturated carbonyl compounds / E. Keinan and N. Greenspoon -- Organometallic derivatives of [alpha], [beta]-unsaturated enones / J.A.S. Howell -- Dienols (enolization of enones) / B. Capon -- Asymmetric synthesis with chiral enones / M.R. Peel and C.R. Johnson -- Dimerization and polymerization of enones in the fluid and solid states / C.R. Theocharis. |
| Record Nr. | UNINA-9910841432303321 |
|
Patai Saul E
|
||
| [Place of publication not identified], : John Wiley & Sons Incorporated, 1989 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Inhibition of premixed carbon monoxide-hydrogen-oxygen-nitrogen flames by iron pentacarbonyl [[electronic resource] /] / Marc D. Rumminger and Gregory T. Linteris
| Inhibition of premixed carbon monoxide-hydrogen-oxygen-nitrogen flames by iron pentacarbonyl [[electronic resource] /] / Marc D. Rumminger and Gregory T. Linteris |
| Autore | Rumminger Marc D |
| Pubbl/distr/stampa | Gaithersburg, Md. : , : U.S. Dept. of Commerce, Technology Administration, National Institute of Standards and Technology, , [1999] |
| Descrizione fisica | 1 online resource (35 pages) : illustrations |
| Altri autori (Persone) | LinterisGregory T |
| Collana | NISTIR |
| Soggetto topico |
Fire extinguishing agents
Carbonyl compounds Combustion - Measurement |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910703073603321 |
|
Rumminger Marc D
|
||
| Gaithersburg, Md. : , : U.S. Dept. of Commerce, Technology Administration, National Institute of Standards and Technology, , [1999] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Soggetto topico
-
Carbonyl compounds
(27)
- Inorganic polymers (3)
- Phosgene (3)
- Functional groups (2)
- Carboxylic acids (1)