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Chemistry and technology of carbodiimides [[electronic resource] /] / Henri Ulrich
| Chemistry and technology of carbodiimides [[electronic resource] /] / Henri Ulrich |
| Autore | Ulrich Henri <1925-> |
| Pubbl/distr/stampa | Chichester, England ; ; Hoboken, NJ, : John Wiley & Sons, 2007 |
| Descrizione fisica | 1 online resource (312 p.) |
| Disciplina | 661/.894 |
| Soggetto topico | Carbodiimides |
| ISBN |
1-282-23753-5
9786612237539 0-470-51668-2 0-470-51667-4 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Chemistry and Technology of Carbodiimides; Contents; Preface; Acknowledgements; 1 General Introduction; 1.1 References; 2 Alkyl- and Arylcarbodiimides; 2.1 Introduction; 2.2 Synthesis of Alkyl- and Arylcarbodiimides; 2.2.1 From Thioureas, Isothioureas and Selenoureas; 2.2.2 By Dehydration of Ureas; 2.2.3 From Isocyanates or Isothiocyanates; 2.2.4 From Cyanamides; 2.2.5 By Nitrene Rearrangements; 2.2.6 From Haloformamidines or Carbonimidoyl Dihalides; 2.2.7 By Thermolysis Reactions; 2.2.8 By Miscellaneous Other Methods; 2.3 References I; 2.4 Reactions of Alkyl- and Arylcarbodiimides
2.4.1 Oligomerization and Polymerization2.4.2 Cycloaddition Reactions; 2.4.3 Reaction of Ylides with Carbodiimides; 2.4.4 Insertion Reactions; 2.4.5 Nucleophilic Reactions; 2.4.6 Heterocycles from Carbodiimides; 2.4.7 Use of Carbodiimides In Condensation Reactions; 2.4.8 Miscellaneous Reactions; 2.5 References II; 3 Unsaturated Carbodiimides; 3.1 Introduction; 3.2 Synthesis of Unsaturated Carbodiimides; 3.2.1 From Thioureas; 3.2.2 From Unsaturated Isocyanates; 3.2.3 From Unsaturated Iminophosphoranes and Isocyanates or Isothiocyanates; 3.2.4 By Other Methods 3.3 Reactions of Unsaturated Carbodiimides3.3.1 Polymerization Reactions; 3.3.2 Cycloaddition Reactions; 3.3.3 Other Reactions; 3.4 References; 4 Halogenated Carbodiimides; 4.1 Introduction; 4.2 Synthesis of Halogenated Carbodiimides; 4.2.1 From -Haloisocyanates; 4.2.2 By Halogenation of Carbodiimides; 4.2.3 From Carbonimidoyl Dichlorides or Imidoyl Chlorides; 4.2.4 By Other Methods; 4.3 Reactions of Halogenated Carbodiimides; 4.3.1 Cycloaddition Reactions; 4.3.2 Nucleophilic Reactions; 4.3.3 Other Reactions; 4.4 References; 5 Acyl-, Thioacyl- and Imidoylcarbodiimides; 5.1 Introduction 5.2 Synthesis of Acyl-, Thioacyl- and Imidoylcarbodiimides5.2.1 From Thioureas; 5.2.2 From Ureas; 5.2.3 From Isocyanates; 5.2.4 From Carbonimidoyl Dichlorides or Chloroformamidines; 5.2.5 From Cyanamides; 5.2.6 From Other Carbodiimides; 5.2.7 By Other Methods; 5.3 Reactions of Acyl-, Thioacyl- and Imidoylcarbodiimides; 5.3.1 Cycloaddition Reactions; 5.3.2 Other Reaction; 5.4 References; 6 Silicon Substituted Carbodiimides; 6.1 Introduction; 6.2 Synthesis of Silicon Substituted Carbodiimides; 6.2.1 From Cyanamides; 6.2.2 From Ureas; 6.2.3 From Isocyanates and Isothiocyanates 6.2.4 From Silylamines6.2.5 From Other Carbodiimides; 6.2.6 By Other Methods; 6.3 Reactions of Silicon Substituted Carbodiimides; 6.3.1 Oligomerization Reactions; 6.3.2 Cycloaddition Reactions; 6.3.3 Other Reactions; 6.4 References; 7 Nitrogen Substituted Carbodiimides; 7.1 Introduction; 7.2 Synthesis of Nitrogen Substituted Carbodiimides; 7.3 Reactions of Nitrogen Substituted Carbodiimides; 7.4 References; 8 Phosphorous Substituted Carbodiimides; 8.1 Introduction; 8.2 Synthesis of Phosphorous Substituted Carbodiimides; 8.2.1 From Thioureas; 8.2.2 From Iminophosphoranes 8.2.3 From Carbonimidoyl Dichlorides |
| Record Nr. | UNINA-9910144291603321 |
Ulrich Henri <1925->
|
||
| Chichester, England ; ; Hoboken, NJ, : John Wiley & Sons, 2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chemistry and technology of carbodiimides / / Henri Ulrich
| Chemistry and technology of carbodiimides / / Henri Ulrich |
| Autore | Ulrich Henri <1925-> |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Chichester, England ; ; Hoboken, NJ, : John Wiley & Sons, 2007 |
| Descrizione fisica | 1 online resource (312 p.) |
| Disciplina | 661/.894 |
| Soggetto topico | Carbodiimides |
| ISBN |
1-282-23753-5
9786612237539 0-470-51668-2 0-470-51667-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Chemistry and Technology of Carbodiimides; Contents; Preface; Acknowledgements; 1 General Introduction; 1.1 References; 2 Alkyl- and Arylcarbodiimides; 2.1 Introduction; 2.2 Synthesis of Alkyl- and Arylcarbodiimides; 2.2.1 From Thioureas, Isothioureas and Selenoureas; 2.2.2 By Dehydration of Ureas; 2.2.3 From Isocyanates or Isothiocyanates; 2.2.4 From Cyanamides; 2.2.5 By Nitrene Rearrangements; 2.2.6 From Haloformamidines or Carbonimidoyl Dihalides; 2.2.7 By Thermolysis Reactions; 2.2.8 By Miscellaneous Other Methods; 2.3 References I; 2.4 Reactions of Alkyl- and Arylcarbodiimides
2.4.1 Oligomerization and Polymerization2.4.2 Cycloaddition Reactions; 2.4.3 Reaction of Ylides with Carbodiimides; 2.4.4 Insertion Reactions; 2.4.5 Nucleophilic Reactions; 2.4.6 Heterocycles from Carbodiimides; 2.4.7 Use of Carbodiimides In Condensation Reactions; 2.4.8 Miscellaneous Reactions; 2.5 References II; 3 Unsaturated Carbodiimides; 3.1 Introduction; 3.2 Synthesis of Unsaturated Carbodiimides; 3.2.1 From Thioureas; 3.2.2 From Unsaturated Isocyanates; 3.2.3 From Unsaturated Iminophosphoranes and Isocyanates or Isothiocyanates; 3.2.4 By Other Methods 3.3 Reactions of Unsaturated Carbodiimides3.3.1 Polymerization Reactions; 3.3.2 Cycloaddition Reactions; 3.3.3 Other Reactions; 3.4 References; 4 Halogenated Carbodiimides; 4.1 Introduction; 4.2 Synthesis of Halogenated Carbodiimides; 4.2.1 From -Haloisocyanates; 4.2.2 By Halogenation of Carbodiimides; 4.2.3 From Carbonimidoyl Dichlorides or Imidoyl Chlorides; 4.2.4 By Other Methods; 4.3 Reactions of Halogenated Carbodiimides; 4.3.1 Cycloaddition Reactions; 4.3.2 Nucleophilic Reactions; 4.3.3 Other Reactions; 4.4 References; 5 Acyl-, Thioacyl- and Imidoylcarbodiimides; 5.1 Introduction 5.2 Synthesis of Acyl-, Thioacyl- and Imidoylcarbodiimides5.2.1 From Thioureas; 5.2.2 From Ureas; 5.2.3 From Isocyanates; 5.2.4 From Carbonimidoyl Dichlorides or Chloroformamidines; 5.2.5 From Cyanamides; 5.2.6 From Other Carbodiimides; 5.2.7 By Other Methods; 5.3 Reactions of Acyl-, Thioacyl- and Imidoylcarbodiimides; 5.3.1 Cycloaddition Reactions; 5.3.2 Other Reaction; 5.4 References; 6 Silicon Substituted Carbodiimides; 6.1 Introduction; 6.2 Synthesis of Silicon Substituted Carbodiimides; 6.2.1 From Cyanamides; 6.2.2 From Ureas; 6.2.3 From Isocyanates and Isothiocyanates 6.2.4 From Silylamines6.2.5 From Other Carbodiimides; 6.2.6 By Other Methods; 6.3 Reactions of Silicon Substituted Carbodiimides; 6.3.1 Oligomerization Reactions; 6.3.2 Cycloaddition Reactions; 6.3.3 Other Reactions; 6.4 References; 7 Nitrogen Substituted Carbodiimides; 7.1 Introduction; 7.2 Synthesis of Nitrogen Substituted Carbodiimides; 7.3 Reactions of Nitrogen Substituted Carbodiimides; 7.4 References; 8 Phosphorous Substituted Carbodiimides; 8.1 Introduction; 8.2 Synthesis of Phosphorous Substituted Carbodiimides; 8.2.1 From Thioureas; 8.2.2 From Iminophosphoranes 8.2.3 From Carbonimidoyl Dichlorides |
| Record Nr. | UNINA-9910828098003321 |
|
Ulrich Henri <1925->
|
||
| Chichester, England ; ; Hoboken, NJ, : John Wiley & Sons, 2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Cumulenes in click reactions [[electronic resource] /] / Henri Ulrich
| Cumulenes in click reactions [[electronic resource] /] / Henri Ulrich |
| Autore | Ulrich Henri <1925-> |
| Pubbl/distr/stampa | Hoboken, NJ, : Wiley, 2009 |
| Descrizione fisica | 1 online resource (566 p.) |
| Disciplina |
547.2
547.412 |
| Soggetto topico |
Alkenes
Chemical reactions |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-46107-9
9786612461071 0-470-74795-1 0-470-74793-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cumulenes in Click Reactions; Contents; Preface; Acknowledgements; 1 General Introduction; References; 2 1-Carbon Cumulenes; 2.1 Sulfines, R2C SO; 2.1.1 Introduction; 2.1.2 Dimerization Reactions; 2.1.3 Cycloaddition Reactions; References; 2.2 Sulfenes, R2C S(O)O; 2.2.1 Introduction; 2.2.2 Dimerization Reactions; 2.2.3 Cycloaddition Reactions; References; 2.3 Other 1-Carbon Cumulenes; 2.3.1 Thiocarbonyl S-Imides; 2.3.2 Thiocarbonyl S-Sulfides; 2.3.3 1-Aza-2-azoniaallene Salts; References; 3 2-Carbon Cumulenes; 3.1 Carbon Oxides, O C O, :CO; 3.1.1 Introduction; 3.1.2 Cycloaddition Reactions
3.1.3 Insertion ReactionsReferences; 3.2 Carbon Sulfides, S C S, S CO; 3.2.1 Introduction; 3.2.2 Cycloaddition Reactions; 3.2.3 Insertion Reactions; References; 3.3 Carbon Nitrides; 3.3.1 Isocyanates, RN CO; References; 3.3.2 Isothiocyanates, RN C S; References; 3.3.3 Carbodiimides, RN C NR; References; 3.4 Center Carbon Phosphorallenes, P C P; 3.4.1 Introduction; 3.4.2 Dimerization Reactions; 3.4.3 Cycloaddition Reactions; References; 4 1,2-Dicarbon Cumulenes; 4.1 Ketenes, R2C C O; 4.1.1 Introduction; 4.1.2 Dimerization Reactions; 4.1.3 Trimerization Reactions; 4.1.4 Cycloaddition Reactions References4.2 Thioketenes, R2C C S; 4.2.1 Introduction; 4.2.2 Dimerization Reactions; 4.2.3 Cycloaddition Reactions; References; 4.3 Ketenimines, R2C C NR; 4.3.1 Introduction; 4.3.2 Dimerization Reactions; 4.3.3 Cycloaddition Reactions; References; 4.4 1-Silaallenes, R2C C Si; 4.4.1 Introduction; 4.4.2 Dimerization Reactions; 4.4.3 Cycloaddition Reactions; References; 4.5 1-Phosphaallenes, R2C C P; 4.5.1 Introduction; 4.5.2 Dimerization Reactions; 4.5.3 Cycloaddition Reactions; References; 4.6 Other Metal Allenes; 4.6.1 Introduction; 4.6.2 Cycloaddition Reactions; References 5 1,3-Dicarbon Cumulenes5.1 Thiocarbonyl S-ylides, R2C S CH2; 5.2 2-Azaallenium Salts, R2C N+ CR2; 5.3 1-Oxa-3-azoniabutatriene Salts, R2C N+ C O; 5.4 1-Thia-3-azabutatriene Salts, R2C N+ C S; 5.5 Phosphorus Ylides; References; 6 1,2,3-Tricarbon Cumulenes; 6.1 Allenes, R2C C CR2; 6.1.1 Introduction; 6.1.2 Dimerization Reactions; 6.1.3 Oligomerization Reactions; 6.1.4 Cycloaddition Reactions; References; 6.2 [3] Cumulenes, R2C C C CR2; 6.2.1 Introduction; 6.2.2 Dimerization Reactions; 6.2.3 Trimerization Reactions; 6.2.4 Cycloaddition Reactions; References; 6.3 [4] Cumulenes, R2C C C C CR2 6.3.1 Introduction6.3.2 Dimerization Reactions; 6.3.3 Cycloaddition Reactions; References; 6.4 [5] Cumulenes, R2C C C C C CR2; 6.4.1 Introduction; 6.4.2 Dimerization Reactions; 6.4.3 Cycloaddition Reactions; References; 7 Noncarbon Cumulenes; 7.1 Azides, RN N N; 7.1.1 Introduction; 7.1.2 Oligomers; 7.1.3 [3+2] Cycloaddition Reactions; References; 7.1.4 Some Applications in Modifications of Biopolymers; Application References; 7.2 Triazaallenium Salts, RN N+ NR; 7.2.1 Introduction; 7.2.2 Cycloaddition Reactions; References; 7.3 Sulfur Oxides; 7.3.1 Introduction; 7.3.2 Sulfur Dioxide, O S O 7.3.3 Sulfur Trioxide, O SO2 |
| Record Nr. | UNINA-9910139957803321 |
|
Ulrich Henri <1925->
|
||
| Hoboken, NJ, : Wiley, 2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Cumulenes in click reactions [[electronic resource] /] / Henri Ulrich
| Cumulenes in click reactions [[electronic resource] /] / Henri Ulrich |
| Autore | Ulrich Henri <1925-> |
| Pubbl/distr/stampa | Hoboken, NJ, : Wiley, 2009 |
| Descrizione fisica | 1 online resource (566 p.) |
| Disciplina |
547.2
547.412 |
| Soggetto topico |
Alkenes
Chemical reactions |
| ISBN |
1-282-46107-9
9786612461071 0-470-74795-1 0-470-74793-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cumulenes in Click Reactions; Contents; Preface; Acknowledgements; 1 General Introduction; References; 2 1-Carbon Cumulenes; 2.1 Sulfines, R2C SO; 2.1.1 Introduction; 2.1.2 Dimerization Reactions; 2.1.3 Cycloaddition Reactions; References; 2.2 Sulfenes, R2C S(O)O; 2.2.1 Introduction; 2.2.2 Dimerization Reactions; 2.2.3 Cycloaddition Reactions; References; 2.3 Other 1-Carbon Cumulenes; 2.3.1 Thiocarbonyl S-Imides; 2.3.2 Thiocarbonyl S-Sulfides; 2.3.3 1-Aza-2-azoniaallene Salts; References; 3 2-Carbon Cumulenes; 3.1 Carbon Oxides, O C O, :CO; 3.1.1 Introduction; 3.1.2 Cycloaddition Reactions
3.1.3 Insertion ReactionsReferences; 3.2 Carbon Sulfides, S C S, S CO; 3.2.1 Introduction; 3.2.2 Cycloaddition Reactions; 3.2.3 Insertion Reactions; References; 3.3 Carbon Nitrides; 3.3.1 Isocyanates, RN CO; References; 3.3.2 Isothiocyanates, RN C S; References; 3.3.3 Carbodiimides, RN C NR; References; 3.4 Center Carbon Phosphorallenes, P C P; 3.4.1 Introduction; 3.4.2 Dimerization Reactions; 3.4.3 Cycloaddition Reactions; References; 4 1,2-Dicarbon Cumulenes; 4.1 Ketenes, R2C C O; 4.1.1 Introduction; 4.1.2 Dimerization Reactions; 4.1.3 Trimerization Reactions; 4.1.4 Cycloaddition Reactions References4.2 Thioketenes, R2C C S; 4.2.1 Introduction; 4.2.2 Dimerization Reactions; 4.2.3 Cycloaddition Reactions; References; 4.3 Ketenimines, R2C C NR; 4.3.1 Introduction; 4.3.2 Dimerization Reactions; 4.3.3 Cycloaddition Reactions; References; 4.4 1-Silaallenes, R2C C Si; 4.4.1 Introduction; 4.4.2 Dimerization Reactions; 4.4.3 Cycloaddition Reactions; References; 4.5 1-Phosphaallenes, R2C C P; 4.5.1 Introduction; 4.5.2 Dimerization Reactions; 4.5.3 Cycloaddition Reactions; References; 4.6 Other Metal Allenes; 4.6.1 Introduction; 4.6.2 Cycloaddition Reactions; References 5 1,3-Dicarbon Cumulenes5.1 Thiocarbonyl S-ylides, R2C S CH2; 5.2 2-Azaallenium Salts, R2C N+ CR2; 5.3 1-Oxa-3-azoniabutatriene Salts, R2C N+ C O; 5.4 1-Thia-3-azabutatriene Salts, R2C N+ C S; 5.5 Phosphorus Ylides; References; 6 1,2,3-Tricarbon Cumulenes; 6.1 Allenes, R2C C CR2; 6.1.1 Introduction; 6.1.2 Dimerization Reactions; 6.1.3 Oligomerization Reactions; 6.1.4 Cycloaddition Reactions; References; 6.2 [3] Cumulenes, R2C C C CR2; 6.2.1 Introduction; 6.2.2 Dimerization Reactions; 6.2.3 Trimerization Reactions; 6.2.4 Cycloaddition Reactions; References; 6.3 [4] Cumulenes, R2C C C C CR2 6.3.1 Introduction6.3.2 Dimerization Reactions; 6.3.3 Cycloaddition Reactions; References; 6.4 [5] Cumulenes, R2C C C C C CR2; 6.4.1 Introduction; 6.4.2 Dimerization Reactions; 6.4.3 Cycloaddition Reactions; References; 7 Noncarbon Cumulenes; 7.1 Azides, RN N N; 7.1.1 Introduction; 7.1.2 Oligomers; 7.1.3 [3+2] Cycloaddition Reactions; References; 7.1.4 Some Applications in Modifications of Biopolymers; Application References; 7.2 Triazaallenium Salts, RN N+ NR; 7.2.1 Introduction; 7.2.2 Cycloaddition Reactions; References; 7.3 Sulfur Oxides; 7.3.1 Introduction; 7.3.2 Sulfur Dioxide, O S O 7.3.3 Sulfur Trioxide, O SO2 |
| Record Nr. | UNINA-9910831093303321 |
|
Ulrich Henri <1925->
|
||
| Hoboken, NJ, : Wiley, 2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Cumulenes in click reactions / / Henri Ulrich
| Cumulenes in click reactions / / Henri Ulrich |
| Autore | Ulrich Henri <1925-> |
| Pubbl/distr/stampa | Hoboken, NJ, : Wiley, 2009 |
| Descrizione fisica | 1 online resource (566 p.) |
| Disciplina |
547.2
547.412 |
| Soggetto topico |
Alkenes
Chemical reactions |
| ISBN |
1-282-46107-9
9786612461071 0-470-74795-1 0-470-74793-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cumulenes in Click Reactions; Contents; Preface; Acknowledgements; 1 General Introduction; References; 2 1-Carbon Cumulenes; 2.1 Sulfines, R2C SO; 2.1.1 Introduction; 2.1.2 Dimerization Reactions; 2.1.3 Cycloaddition Reactions; References; 2.2 Sulfenes, R2C S(O)O; 2.2.1 Introduction; 2.2.2 Dimerization Reactions; 2.2.3 Cycloaddition Reactions; References; 2.3 Other 1-Carbon Cumulenes; 2.3.1 Thiocarbonyl S-Imides; 2.3.2 Thiocarbonyl S-Sulfides; 2.3.3 1-Aza-2-azoniaallene Salts; References; 3 2-Carbon Cumulenes; 3.1 Carbon Oxides, O C O, :CO; 3.1.1 Introduction; 3.1.2 Cycloaddition Reactions
3.1.3 Insertion ReactionsReferences; 3.2 Carbon Sulfides, S C S, S CO; 3.2.1 Introduction; 3.2.2 Cycloaddition Reactions; 3.2.3 Insertion Reactions; References; 3.3 Carbon Nitrides; 3.3.1 Isocyanates, RN CO; References; 3.3.2 Isothiocyanates, RN C S; References; 3.3.3 Carbodiimides, RN C NR; References; 3.4 Center Carbon Phosphorallenes, P C P; 3.4.1 Introduction; 3.4.2 Dimerization Reactions; 3.4.3 Cycloaddition Reactions; References; 4 1,2-Dicarbon Cumulenes; 4.1 Ketenes, R2C C O; 4.1.1 Introduction; 4.1.2 Dimerization Reactions; 4.1.3 Trimerization Reactions; 4.1.4 Cycloaddition Reactions References4.2 Thioketenes, R2C C S; 4.2.1 Introduction; 4.2.2 Dimerization Reactions; 4.2.3 Cycloaddition Reactions; References; 4.3 Ketenimines, R2C C NR; 4.3.1 Introduction; 4.3.2 Dimerization Reactions; 4.3.3 Cycloaddition Reactions; References; 4.4 1-Silaallenes, R2C C Si; 4.4.1 Introduction; 4.4.2 Dimerization Reactions; 4.4.3 Cycloaddition Reactions; References; 4.5 1-Phosphaallenes, R2C C P; 4.5.1 Introduction; 4.5.2 Dimerization Reactions; 4.5.3 Cycloaddition Reactions; References; 4.6 Other Metal Allenes; 4.6.1 Introduction; 4.6.2 Cycloaddition Reactions; References 5 1,3-Dicarbon Cumulenes5.1 Thiocarbonyl S-ylides, R2C S CH2; 5.2 2-Azaallenium Salts, R2C N+ CR2; 5.3 1-Oxa-3-azoniabutatriene Salts, R2C N+ C O; 5.4 1-Thia-3-azabutatriene Salts, R2C N+ C S; 5.5 Phosphorus Ylides; References; 6 1,2,3-Tricarbon Cumulenes; 6.1 Allenes, R2C C CR2; 6.1.1 Introduction; 6.1.2 Dimerization Reactions; 6.1.3 Oligomerization Reactions; 6.1.4 Cycloaddition Reactions; References; 6.2 [3] Cumulenes, R2C C C CR2; 6.2.1 Introduction; 6.2.2 Dimerization Reactions; 6.2.3 Trimerization Reactions; 6.2.4 Cycloaddition Reactions; References; 6.3 [4] Cumulenes, R2C C C C CR2 6.3.1 Introduction6.3.2 Dimerization Reactions; 6.3.3 Cycloaddition Reactions; References; 6.4 [5] Cumulenes, R2C C C C C CR2; 6.4.1 Introduction; 6.4.2 Dimerization Reactions; 6.4.3 Cycloaddition Reactions; References; 7 Noncarbon Cumulenes; 7.1 Azides, RN N N; 7.1.1 Introduction; 7.1.2 Oligomers; 7.1.3 [3+2] Cycloaddition Reactions; References; 7.1.4 Some Applications in Modifications of Biopolymers; Application References; 7.2 Triazaallenium Salts, RN N+ NR; 7.2.1 Introduction; 7.2.2 Cycloaddition Reactions; References; 7.3 Sulfur Oxides; 7.3.1 Introduction; 7.3.2 Sulfur Dioxide, O S O 7.3.3 Sulfur Trioxide, O SO2 |
| Record Nr. | UNINA-9910877710203321 |
|
Ulrich Henri <1925->
|
||
| Hoboken, NJ, : Wiley, 2009 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||