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The Chemistry of Heterocyclic Compounds, since its inception, has been recognized as a cornerstone of heterocyclic chemistry. Each volume attempts to discuss all aspects - properties, synthesis, reactions, physiological and industrial significance - of a specific ring system. To keep the series up-to-date, supplementary volumes covering the recent literature on each individual ring system have been published. Many ring systems (such as pyridines and oxazoles) are treated in distinct books, each consisting of separate volumes or parts dealing with different individual topics. With all authors…mehr
The Chemistry of Heterocyclic Compounds, since its inception, has been recognized as a cornerstone of heterocyclic chemistry. Each volume attempts to discuss all aspects - properties, synthesis, reactions, physiological and industrial significance - of a specific ring system. To keep the series up-to-date, supplementary volumes covering the recent literature on each individual ring system have been published. Many ring systems (such as pyridines and oxazoles) are treated in distinct books, each consisting of separate volumes or parts dealing with different individual topics. With all authors are recognized authorities, the Chemistry of Heterocyclic Chemistry is considered worldwide as the indispensable resource for organic, bioorganic, and medicinal chemists.
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Klaus Hofmann is the editor of Imidazole and Its Derivatives, Part 1, Volume 6, published by Wiley.
Inhaltsangabe
Preface ix Section I Chemistry of Classes and Derivatives I. General Properties and Structure of the Imidazoles 3 A. Nomenclature 3 B. Physical Properties 5 C. Chemical Properties 13 D. Structural Considerations 17 E. Tautomeric Character 26 II. The Alkyl- and Arylimidazoles 33 A. Synthetic Procedures 33 B. Properties and Chemical Behavior 45 III. The Oxo- and Hydroxyimidazoles and Their Sulfur Analogues 55 A. The Oxoimidazoles 55 B. The Hydroxyalkylimidazoles 99 IV. The Halogenoimidazoles 111 A. Bromoimidazoles 111 B. Chloroimidazoles 119 C. Chloroalky limidazoles 121 V. The Nitro-, Arylazo-, and Aminoimidazoles 127 A. Nitroimidazoles 127 B. Arylazoimidazolcs 136 C. Aminoimidazoles 141 D. Histamine 143 VI. The Imidazolecarboxylic and Sulfonic Acids 175 A. Imidazolecarhoxylic Acids 175 B. Imidazolesulfonic Acids 206 VII. The Imidazolines, 2-Imidazolidones, 2-Imidazolidinethiones, 2-Iminoimidazolidines, and Imidazolidines 213 A. Nomenclature 213 B. 2-ImidazoIines 213 C. 2-Imidazolidones 226 D. 2-Imidazolidinethiones 234 E. 2-Iminoimidazolidines 238 F. Imidazolidines 242 VIII. The Benzimidazoles 247 A Nomenclature 247 B General Properties 248 C. Synthetic Procedures 258 D. The 1-Acylbenzimidazoles and tire Bamberger Reaction 273 E. The Alkyl- and Arylbenzimidazoles and 1,3-Dialkyibenzimiduzolium Salts 276 F. The Oxo- and Hydroxybenzimidazolcs and Their Sulfur Analogues 284 G The Halogenobenzimidazoles 300 H The Nitro- and Aminobenzimidazoles 304 I. The Benzimidazolecarboxylic and Sulfonic Acids 313 Section 2 Systematic Survey and Bibliography Key to Abbreviations 320 I. Imidazoles 327 A. Alkyl-and Arylimidazoles 327 B Alkyl- and Arylimidazolium Salts 330 C. Oxo- and Hydroxyimidazolos and Their Sulfur Analogues 330 D. Halogenoimidazoles 342 E. Nitroimidazoles 345 F. Arylazoimidazoles 346 G. Aminoimidazoles 347 H. Cyano- and Isocyanatoimidazolcs 351 I. Tinidazolcearboxylic Acids 352 J. Imidnzolcsulftnic and Sulfonic Acids 363 K. Imidazole Arscnicals 363 L. Isoimidazolcs 363 M. Heteroring-Substituted Imidazoles 364 N Bi- and Bisimidazoles 366 II. Imidazolines 367 A. 2-Tmidazolines 367 B. 3-Imidazolines 372 C. 4-Imidazolines 372 D. Heteroring-Substituted 2-Imiriaznliiics 372 III. Imidazolidines 373 A. Alkyl- and Arylimidazolidines 373 B. 4- and 5-Imidazolidones 378 C. 2-Iraidazolidinethiones (Ethylenethioureas) 378 D. 4-Imidazolidinethiones 379 E. 2-Iminoimiriazoliriines (Ethyleneguanidines) 379 V. Benzimidazoles 379 A. Alkyl- and Arylbenrimidazoles 379 B. Alkyl- and Arylbenzimidazolium Salts 382 C. Oxo-and Hydroxybenzimidazoles and Their Sulfur Analogues 382 D. Halogeno-, Halogenoalkyl-, and Halogenoarylbenzimidazoles 388 E. Nitro-, Nitroalkyl-, and Nitroarylbenzimidazoles Including Those Containing Additional Functional Groups 388 F. Aminobenzimidazoles 389 G. Cyanobenzimidazoles 394 H Benzimidazolecarboxylic Acids 395 I. Benzimidazolcsulfonic Acids, Sulfoalkyl-, and Sulfoarylbenzimidazoles 398 J. Benzimidazole Arscnicals 398 K. 2,3-DihydroIxaizimidazoles (Benzimidizolines) 399 L. Heteroring-Substituted Benzimidazoles 399 M Bi-, Di-, and Bisbonzimidazoles 401 Bibliography 401 Subject Index 421
Preface ix Section I Chemistry of Classes and Derivatives I. General Properties and Structure of the Imidazoles 3 A. Nomenclature 3 B. Physical Properties 5 C. Chemical Properties 13 D. Structural Considerations 17 E. Tautomeric Character 26 II. The Alkyl- and Arylimidazoles 33 A. Synthetic Procedures 33 B. Properties and Chemical Behavior 45 III. The Oxo- and Hydroxyimidazoles and Their Sulfur Analogues 55 A. The Oxoimidazoles 55 B. The Hydroxyalkylimidazoles 99 IV. The Halogenoimidazoles 111 A. Bromoimidazoles 111 B. Chloroimidazoles 119 C. Chloroalky limidazoles 121 V. The Nitro-, Arylazo-, and Aminoimidazoles 127 A. Nitroimidazoles 127 B. Arylazoimidazolcs 136 C. Aminoimidazoles 141 D. Histamine 143 VI. The Imidazolecarboxylic and Sulfonic Acids 175 A. Imidazolecarhoxylic Acids 175 B. Imidazolesulfonic Acids 206 VII. The Imidazolines, 2-Imidazolidones, 2-Imidazolidinethiones, 2-Iminoimidazolidines, and Imidazolidines 213 A. Nomenclature 213 B. 2-ImidazoIines 213 C. 2-Imidazolidones 226 D. 2-Imidazolidinethiones 234 E. 2-Iminoimidazolidines 238 F. Imidazolidines 242 VIII. The Benzimidazoles 247 A Nomenclature 247 B General Properties 248 C. Synthetic Procedures 258 D. The 1-Acylbenzimidazoles and tire Bamberger Reaction 273 E. The Alkyl- and Arylbenzimidazoles and 1,3-Dialkyibenzimiduzolium Salts 276 F. The Oxo- and Hydroxybenzimidazolcs and Their Sulfur Analogues 284 G The Halogenobenzimidazoles 300 H The Nitro- and Aminobenzimidazoles 304 I. The Benzimidazolecarboxylic and Sulfonic Acids 313 Section 2 Systematic Survey and Bibliography Key to Abbreviations 320 I. Imidazoles 327 A. Alkyl-and Arylimidazoles 327 B Alkyl- and Arylimidazolium Salts 330 C. Oxo- and Hydroxyimidazolos and Their Sulfur Analogues 330 D. Halogenoimidazoles 342 E. Nitroimidazoles 345 F. Arylazoimidazoles 346 G. Aminoimidazoles 347 H. Cyano- and Isocyanatoimidazolcs 351 I. Tinidazolcearboxylic Acids 352 J. Imidnzolcsulftnic and Sulfonic Acids 363 K. Imidazole Arscnicals 363 L. Isoimidazolcs 363 M. Heteroring-Substituted Imidazoles 364 N Bi- and Bisimidazoles 366 II. Imidazolines 367 A. 2-Tmidazolines 367 B. 3-Imidazolines 372 C. 4-Imidazolines 372 D. Heteroring-Substituted 2-Imiriaznliiics 372 III. Imidazolidines 373 A. Alkyl- and Arylimidazolidines 373 B. 4- and 5-Imidazolidones 378 C. 2-Iraidazolidinethiones (Ethylenethioureas) 378 D. 4-Imidazolidinethiones 379 E. 2-Iminoimiriazoliriines (Ethyleneguanidines) 379 V. Benzimidazoles 379 A. Alkyl- and Arylbenrimidazoles 379 B. Alkyl- and Arylbenzimidazolium Salts 382 C. Oxo-and Hydroxybenzimidazoles and Their Sulfur Analogues 382 D. Halogeno-, Halogenoalkyl-, and Halogenoarylbenzimidazoles 388 E. Nitro-, Nitroalkyl-, and Nitroarylbenzimidazoles Including Those Containing Additional Functional Groups 388 F. Aminobenzimidazoles 389 G. Cyanobenzimidazoles 394 H Benzimidazolecarboxylic Acids 395 I. Benzimidazolcsulfonic Acids, Sulfoalkyl-, and Sulfoarylbenzimidazoles 398 J. Benzimidazole Arscnicals 398 K. 2,3-DihydroIxaizimidazoles (Benzimidizolines) 399 L. Heteroring-Substituted Benzimidazoles 399 M Bi-, Di-, and Bisbonzimidazoles 401 Bibliography 401 Subject Index 421
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