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Phosgenations [[electronic resource] ] : a handbook / / L. Cotarca, H. Eckert
Phosgenations [[electronic resource] ] : a handbook / / L. Cotarca, H. Eckert
Autore Cotarca L (Livius)
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2004
Descrizione fisica 1 online resource (670 p.)
Disciplina 661.06812
661.891
Altri autori (Persone) EckertH (Heiner)
Soggetto topico Phosgene
Carbonyl compounds
ISBN 1-280-52018-3
9786610520183
3-527-60503-7
3-527-60262-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Phosgenations - A Handbook; Contents; Preface; 1 Contradictions; References; 2 Phosgenation Reagents; 2.1 Phosgene; 2.1.1 Conventional Manufacturing Processes; 2.1.2 Manufacturing Processes "On Demand of Consumer"; 2.2 Phosgene "Oligomers"; 2.2.1 Diphosgene; 2.2.2 Triphosgene; 2.2.2.1 Triphosgene as a Phosgene Equivalent or Phosgene Source; 2.2.2.2 Stability: Thermally and Chemically Induced Decomposition; 2.2.2.3 Preparation; 2.3 Other Phosgene Equivalents and Substitutes; 2.3.1 Oxalyl Chloride; 2.3.2 1,1-Carbonyldiimidazole; 2.3.3 Dimethyl Carbonate (DMC); 2.4 References
3 Evaluation of Phosgenation Reagents3.1 Definition; 3.2 Reactivity; 3.3 Physical Properties; 3.4 Physiological Data; 3.5 References; 4 Phosgenation Reactions; 4.1 Classification of Phosgenation Reactions; 4.2 Chloroformylation (Chlorocarbonylation); 4.2.1 Chloroformates (Chlorocarbonylation of Alcohols); 4.2.2 Carbamoyl Chlorides (Chlorocarbonylation of Amines); 4.2.2.1 Reactions with Primary Amines; 4.2.2.2 Reactions with Secondary Amines; 4.2.2.3 Reactions with Tertiary Amines; 4.2.2.4 Reactions with Amides; 4.3 Carbonylation; 4.3.1 Isocyanates; 4.3.1.1 Introduction
4.3.1.2 Aromatic Isocyanates4.3.1.3 Alkyl and Alkenyl Isocyanates; 4.3.1.4 Heterocyclic Isocyanates; 4.3.1.5 Isocyanates of Amino Acids; 4.3.1.6 Acyl Isocyanates; 4.3.1.7 Silane Isocyanates; 4.3.2 Carbamates; 4.3.2.1 Phosgene and Haloformates as Reagents; 4.3.2.2 Carbamates Prepared with Isocyanates or Carbamoyl Chlorides; 4.3.2.3 Carbamates Prepared with N,N ́-Carbonyldiimidazole (CDI); 4.3.2.4 Carbamates by Aminolysis of Carbonate or Dithiocarbonate Esters; 4.3.2.5 Enol Carbamates; 4.3.2.6 Carbamates from Isocyanides; 4.3.2.7 Potassium Carbonate as a Carbonylating Reagent
4.3.2.8 Carbamates Prepared with Acryloyl Azide4.3.2.9 Carbon Monoxide; 4.3.2.10 Carbon Dioxide; 4.3.2.11 Sodium Nitrite/HCl; 4.3.3 Carbonates; 4.3.3.1 Chloroformates; 4.3.3.2 Phosgene; 4.3.3.3 Diphosgene; 4.3.3.4 Triphosgene; 4.3.3.5 Carbonyldiimidazole (CDI); 4.3.3.6 Acyl Carbonates; 4.3.3.7 Carbonates (Interchanges); 4.3.3.8 Carbon Oxides, CO, CO(2), and MCO(3); 4.3.3.9 Ureas; 4.3.3.10 Enzyme Catalysis; 4.3.4 Ureas; 4.3.4.1 Phosgene and Symmetrical Phosgene Equivalents; 4.3.4.2 Unsymmetrical Phosgene Equivalents; 4.3.4.3 Carbon Monoxide; 4.3.4.4 Carbon Dioxide; 4.3.4.5 Organic Carbonates
4.3.4.6 Aminolysis of S-Methylthiocarbamates Prepared from Carbonimidodithioates4.3.4.7 Diiodosilane Method; 4.3.4.8 N-Alkylation of Simple Ureas; 4.3.4.9 The Reductive Amination of Aldehydes with Monoalkylureas; 4.3.4.10 Catalytic [Ru(PPh(3))(3)] Aminolysis of Formamides; 4.3.4.11 HY Zeolite HSZ-360 Catalyzed Aminolysis of Acetoacetanilides; 4.3.5 Reactions with Binucleophiles; 4.3.5.1 N,O- and N,S-Binucleophiles. Formation of Oxazolidin-2-ones and Thiazolidin-2-ones; 4.3.5.2 N,N-Binucleophiles. Formation of 2-Oxoimidazolidines; 4.3.5.3 O,O-Binucleophiles. Formation of Cyclic Carbonates
4.3.5.4 N,COOH Binucleophiles. Formation of N-Carboxyanhydrides of α-Amino Acids
Record Nr. UNINA-9910146054103321
Cotarca L (Livius)  
Weinheim, : Wiley-VCH, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Phosgenations [[electronic resource] ] : a handbook / / L. Cotarca, H. Eckert
Phosgenations [[electronic resource] ] : a handbook / / L. Cotarca, H. Eckert
Autore Cotarca L (Livius)
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2004
Descrizione fisica 1 online resource (670 p.)
Disciplina 661.06812
661.891
Altri autori (Persone) EckertH (Heiner)
Soggetto topico Phosgene
Carbonyl compounds
ISBN 1-280-52018-3
9786610520183
3-527-60503-7
3-527-60262-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Phosgenations - A Handbook; Contents; Preface; 1 Contradictions; References; 2 Phosgenation Reagents; 2.1 Phosgene; 2.1.1 Conventional Manufacturing Processes; 2.1.2 Manufacturing Processes "On Demand of Consumer"; 2.2 Phosgene "Oligomers"; 2.2.1 Diphosgene; 2.2.2 Triphosgene; 2.2.2.1 Triphosgene as a Phosgene Equivalent or Phosgene Source; 2.2.2.2 Stability: Thermally and Chemically Induced Decomposition; 2.2.2.3 Preparation; 2.3 Other Phosgene Equivalents and Substitutes; 2.3.1 Oxalyl Chloride; 2.3.2 1,1-Carbonyldiimidazole; 2.3.3 Dimethyl Carbonate (DMC); 2.4 References
3 Evaluation of Phosgenation Reagents3.1 Definition; 3.2 Reactivity; 3.3 Physical Properties; 3.4 Physiological Data; 3.5 References; 4 Phosgenation Reactions; 4.1 Classification of Phosgenation Reactions; 4.2 Chloroformylation (Chlorocarbonylation); 4.2.1 Chloroformates (Chlorocarbonylation of Alcohols); 4.2.2 Carbamoyl Chlorides (Chlorocarbonylation of Amines); 4.2.2.1 Reactions with Primary Amines; 4.2.2.2 Reactions with Secondary Amines; 4.2.2.3 Reactions with Tertiary Amines; 4.2.2.4 Reactions with Amides; 4.3 Carbonylation; 4.3.1 Isocyanates; 4.3.1.1 Introduction
4.3.1.2 Aromatic Isocyanates4.3.1.3 Alkyl and Alkenyl Isocyanates; 4.3.1.4 Heterocyclic Isocyanates; 4.3.1.5 Isocyanates of Amino Acids; 4.3.1.6 Acyl Isocyanates; 4.3.1.7 Silane Isocyanates; 4.3.2 Carbamates; 4.3.2.1 Phosgene and Haloformates as Reagents; 4.3.2.2 Carbamates Prepared with Isocyanates or Carbamoyl Chlorides; 4.3.2.3 Carbamates Prepared with N,N ́-Carbonyldiimidazole (CDI); 4.3.2.4 Carbamates by Aminolysis of Carbonate or Dithiocarbonate Esters; 4.3.2.5 Enol Carbamates; 4.3.2.6 Carbamates from Isocyanides; 4.3.2.7 Potassium Carbonate as a Carbonylating Reagent
4.3.2.8 Carbamates Prepared with Acryloyl Azide4.3.2.9 Carbon Monoxide; 4.3.2.10 Carbon Dioxide; 4.3.2.11 Sodium Nitrite/HCl; 4.3.3 Carbonates; 4.3.3.1 Chloroformates; 4.3.3.2 Phosgene; 4.3.3.3 Diphosgene; 4.3.3.4 Triphosgene; 4.3.3.5 Carbonyldiimidazole (CDI); 4.3.3.6 Acyl Carbonates; 4.3.3.7 Carbonates (Interchanges); 4.3.3.8 Carbon Oxides, CO, CO(2), and MCO(3); 4.3.3.9 Ureas; 4.3.3.10 Enzyme Catalysis; 4.3.4 Ureas; 4.3.4.1 Phosgene and Symmetrical Phosgene Equivalents; 4.3.4.2 Unsymmetrical Phosgene Equivalents; 4.3.4.3 Carbon Monoxide; 4.3.4.4 Carbon Dioxide; 4.3.4.5 Organic Carbonates
4.3.4.6 Aminolysis of S-Methylthiocarbamates Prepared from Carbonimidodithioates4.3.4.7 Diiodosilane Method; 4.3.4.8 N-Alkylation of Simple Ureas; 4.3.4.9 The Reductive Amination of Aldehydes with Monoalkylureas; 4.3.4.10 Catalytic [Ru(PPh(3))(3)] Aminolysis of Formamides; 4.3.4.11 HY Zeolite HSZ-360 Catalyzed Aminolysis of Acetoacetanilides; 4.3.5 Reactions with Binucleophiles; 4.3.5.1 N,O- and N,S-Binucleophiles. Formation of Oxazolidin-2-ones and Thiazolidin-2-ones; 4.3.5.2 N,N-Binucleophiles. Formation of 2-Oxoimidazolidines; 4.3.5.3 O,O-Binucleophiles. Formation of Cyclic Carbonates
4.3.5.4 N,COOH Binucleophiles. Formation of N-Carboxyanhydrides of α-Amino Acids
Record Nr. UNINA-9910831078703321
Cotarca L (Livius)  
Weinheim, : Wiley-VCH, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Phosgenations [[electronic resource] ] : a handbook / / L. Cotarca, H. Eckert
Phosgenations [[electronic resource] ] : a handbook / / L. Cotarca, H. Eckert
Autore Cotarca L (Livius)
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2004
Descrizione fisica 1 online resource (670 p.)
Disciplina 661.06812
661.891
Altri autori (Persone) EckertH (Heiner)
Soggetto topico Phosgene
Carbonyl compounds
ISBN 1-280-52018-3
9786610520183
3-527-60503-7
3-527-60262-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Phosgenations - A Handbook; Contents; Preface; 1 Contradictions; References; 2 Phosgenation Reagents; 2.1 Phosgene; 2.1.1 Conventional Manufacturing Processes; 2.1.2 Manufacturing Processes "On Demand of Consumer"; 2.2 Phosgene "Oligomers"; 2.2.1 Diphosgene; 2.2.2 Triphosgene; 2.2.2.1 Triphosgene as a Phosgene Equivalent or Phosgene Source; 2.2.2.2 Stability: Thermally and Chemically Induced Decomposition; 2.2.2.3 Preparation; 2.3 Other Phosgene Equivalents and Substitutes; 2.3.1 Oxalyl Chloride; 2.3.2 1,1-Carbonyldiimidazole; 2.3.3 Dimethyl Carbonate (DMC); 2.4 References
3 Evaluation of Phosgenation Reagents3.1 Definition; 3.2 Reactivity; 3.3 Physical Properties; 3.4 Physiological Data; 3.5 References; 4 Phosgenation Reactions; 4.1 Classification of Phosgenation Reactions; 4.2 Chloroformylation (Chlorocarbonylation); 4.2.1 Chloroformates (Chlorocarbonylation of Alcohols); 4.2.2 Carbamoyl Chlorides (Chlorocarbonylation of Amines); 4.2.2.1 Reactions with Primary Amines; 4.2.2.2 Reactions with Secondary Amines; 4.2.2.3 Reactions with Tertiary Amines; 4.2.2.4 Reactions with Amides; 4.3 Carbonylation; 4.3.1 Isocyanates; 4.3.1.1 Introduction
4.3.1.2 Aromatic Isocyanates4.3.1.3 Alkyl and Alkenyl Isocyanates; 4.3.1.4 Heterocyclic Isocyanates; 4.3.1.5 Isocyanates of Amino Acids; 4.3.1.6 Acyl Isocyanates; 4.3.1.7 Silane Isocyanates; 4.3.2 Carbamates; 4.3.2.1 Phosgene and Haloformates as Reagents; 4.3.2.2 Carbamates Prepared with Isocyanates or Carbamoyl Chlorides; 4.3.2.3 Carbamates Prepared with N,N ́-Carbonyldiimidazole (CDI); 4.3.2.4 Carbamates by Aminolysis of Carbonate or Dithiocarbonate Esters; 4.3.2.5 Enol Carbamates; 4.3.2.6 Carbamates from Isocyanides; 4.3.2.7 Potassium Carbonate as a Carbonylating Reagent
4.3.2.8 Carbamates Prepared with Acryloyl Azide4.3.2.9 Carbon Monoxide; 4.3.2.10 Carbon Dioxide; 4.3.2.11 Sodium Nitrite/HCl; 4.3.3 Carbonates; 4.3.3.1 Chloroformates; 4.3.3.2 Phosgene; 4.3.3.3 Diphosgene; 4.3.3.4 Triphosgene; 4.3.3.5 Carbonyldiimidazole (CDI); 4.3.3.6 Acyl Carbonates; 4.3.3.7 Carbonates (Interchanges); 4.3.3.8 Carbon Oxides, CO, CO(2), and MCO(3); 4.3.3.9 Ureas; 4.3.3.10 Enzyme Catalysis; 4.3.4 Ureas; 4.3.4.1 Phosgene and Symmetrical Phosgene Equivalents; 4.3.4.2 Unsymmetrical Phosgene Equivalents; 4.3.4.3 Carbon Monoxide; 4.3.4.4 Carbon Dioxide; 4.3.4.5 Organic Carbonates
4.3.4.6 Aminolysis of S-Methylthiocarbamates Prepared from Carbonimidodithioates4.3.4.7 Diiodosilane Method; 4.3.4.8 N-Alkylation of Simple Ureas; 4.3.4.9 The Reductive Amination of Aldehydes with Monoalkylureas; 4.3.4.10 Catalytic [Ru(PPh(3))(3)] Aminolysis of Formamides; 4.3.4.11 HY Zeolite HSZ-360 Catalyzed Aminolysis of Acetoacetanilides; 4.3.5 Reactions with Binucleophiles; 4.3.5.1 N,O- and N,S-Binucleophiles. Formation of Oxazolidin-2-ones and Thiazolidin-2-ones; 4.3.5.2 N,N-Binucleophiles. Formation of 2-Oxoimidazolidines; 4.3.5.3 O,O-Binucleophiles. Formation of Cyclic Carbonates
4.3.5.4 N,COOH Binucleophiles. Formation of N-Carboxyanhydrides of α-Amino Acids
Record Nr. UNINA-9910841350703321
Cotarca L (Livius)  
Weinheim, : Wiley-VCH, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui