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Benzofurans [[electronic resource]]
Benzofurans [[electronic resource]]
Autore Mustafa Ahmed <1918->
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Wiley, 1974
Descrizione fisica 1 online resource (538 p.)
Disciplina 547.592
547/.59/05
547/.592
Collana The Chemistry of heterocyclic compounds
Soggetto topico Benzofuran
Heterocyclic compounds
ISBN 1-282-30174-8
9786612301742
0-470-18699-2
0-470-18850-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Matter; Preface; Contents; I. Benzofurans; 1. Introduction and Nomenclature; 2. Benzofuran and Its Alkyl Derivatives; A. Preparation; a. Catalytic Dehydrocyclization; b. Cyclizution of Allylphenols; c. Cyclodehydration of Ary foxy ketones; d. Rearrangement of' O-Aryloximes; e. Dehydrogenation of Bz-AIkyldihydrobenzofurans; f. Reduction of 2-Acetonyl-o-benzoquinols; g. Hydrogenation of 2-Acetylbenzofuran; h. Reaction of Copper Acetylides with Aryl Halides; i. Decarboxylation of Benzofurancarboxylic Acids; j. Photochemical Formation of Benzofurans; k. Adsorptive Cyclization
l. Condensation of Methylene Bis (ethyl sulfone)with Salicylaldehydes3. Aryl benzofurans; A. Preparation; a. Cychdehydration of w-Arloxyacetophenones; b. Condensation of Benzoins with Phenols; c. 1,3-Dipolar Additions of Oxocarbenes; d. Copper-Catalyzed Decomposition of Diazoketones; e. Ethynation of P-Benzoquinone; f Oxidation of Flavylium and Pyrylium Salts; g. Algar-Flynn-Oyamada Oxidation of 2'-Hydroxychalcones; h. Acid-Catalyzed Cyclization of O-Aryloximes; i. Photolytic Cyclizalions.; j. Miscellaneous; 4. Halobenzofurans; A. Caloro Derivatives; B. Bromo Derivatives; C. Iodo Derivatives
D. Fluoro Derivatives5. Nitrobenzofurans; 6. Benzofuranols; 7. Aminobenzofurans; 8. Benzofuranquinones; 9. Miscellaneous Reactions and Properties; A. Catalytic Hydrogenation; B. Oxidation; C. Ozonolysis; D. Nitration; E. Halogenation; F. Benzofuranylmetallic Compounds; G. Friedel-Crafts Techniques; H. Hoesch and Gatterman Techniques; I. With Diazoalkanes; J. With Dihalocarbene; K. Cyclophotochemical Addition; L. Polymerization; M. Miscellaneous Reactions; References; II. Acylbenzofurans; 1. Formylbenzofurans; 2. Acylbenzofurans; 3. Miscellaneous reactions; A. Reduction; B. Oxidation
C. Alkaline DegradationD. Rearrangement of Acylbenzofuran Oximes; E. Rearrangement (Migration) in Acylbenzofurans; F. Willgerodt-Kindler Reaction; G. Wittig Reaction; H. Miscellaneous; References; III. Benzofurancarboxylic acids; 1. Benzofuran monocarboxylic Acids; A. 2-Benzofurancarboxylic Acids; B. 3-Benzofurancarboxylic Acids; C. Hydroxybenzofurancarboxylic Acids; 2. Benzofuran Dicarboxylic Acids; 3. Benzofuranylalkanoic Acids; A. Benzofuranylacetic Acids; B. Benzofuranylpropionic Acids; C. Benzofuranylbutyric Acids; D. Miscellaneous Benzofuranylalkanoic Acids
4. Miscellaneous Reactions of Benzofurancarboxylic AcidsA. Halogenation; B. Chloromethylation; C. Nitration; D. Saponification; E. Catalytic Hydrogenation; F. Peroxide Formation and Ozonolysis; G. Acylation; H. Alkylation; I. Miscellaneous Reactions; References; IV. Hydrogenated Benzofurans; 1. Dihydrobenzofurans; A. Alkyl- (or Aryl-) Substituted 2.3-Dihydrobenzofurans; B. Halogen-Substituted 2,3-Dihydrobenzofurans; C. Nitro-Substituted 2,3-Dihydrobenzofurans; D. Amino-Substituted 2,3-Dihydrobenzofurans; E. 2.3-Dihydrobenzofuranols; F. Geometrical Isomers of 2,3-Dihydrobenzofurans
G. Miscellaneous Reactions of 2,3-Dihydrobenzofurans
Record Nr. UNINA-9910144280803321
Mustafa Ahmed <1918->  
New York, : Wiley, 1974
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Benzofurans [[electronic resource]]
Benzofurans [[electronic resource]]
Autore Mustafa Ahmed <1918->
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Wiley, 1974
Descrizione fisica 1 online resource (538 p.)
Disciplina 547.592
547/.59/05
547/.592
Collana The Chemistry of heterocyclic compounds
Soggetto topico Benzofuran - lemac
Heterocyclic compounds
ISBN 1-282-30174-8
9786612301742
0-470-18699-2
0-470-18850-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Matter; Preface; Contents; I. Benzofurans; 1. Introduction and Nomenclature; 2. Benzofuran and Its Alkyl Derivatives; A. Preparation; a. Catalytic Dehydrocyclization; b. Cyclizution of Allylphenols; c. Cyclodehydration of Ary foxy ketones; d. Rearrangement of' O-Aryloximes; e. Dehydrogenation of Bz-AIkyldihydrobenzofurans; f. Reduction of 2-Acetonyl-o-benzoquinols; g. Hydrogenation of 2-Acetylbenzofuran; h. Reaction of Copper Acetylides with Aryl Halides; i. Decarboxylation of Benzofurancarboxylic Acids; j. Photochemical Formation of Benzofurans; k. Adsorptive Cyclization
l. Condensation of Methylene Bis (ethyl sulfone)with Salicylaldehydes3. Aryl benzofurans; A. Preparation; a. Cychdehydration of w-Arloxyacetophenones; b. Condensation of Benzoins with Phenols; c. 1,3-Dipolar Additions of Oxocarbenes; d. Copper-Catalyzed Decomposition of Diazoketones; e. Ethynation of P-Benzoquinone; f Oxidation of Flavylium and Pyrylium Salts; g. Algar-Flynn-Oyamada Oxidation of 2'-Hydroxychalcones; h. Acid-Catalyzed Cyclization of O-Aryloximes; i. Photolytic Cyclizalions.; j. Miscellaneous; 4. Halobenzofurans; A. Caloro Derivatives; B. Bromo Derivatives; C. Iodo Derivatives
D. Fluoro Derivatives5. Nitrobenzofurans; 6. Benzofuranols; 7. Aminobenzofurans; 8. Benzofuranquinones; 9. Miscellaneous Reactions and Properties; A. Catalytic Hydrogenation; B. Oxidation; C. Ozonolysis; D. Nitration; E. Halogenation; F. Benzofuranylmetallic Compounds; G. Friedel-Crafts Techniques; H. Hoesch and Gatterman Techniques; I. With Diazoalkanes; J. With Dihalocarbene; K. Cyclophotochemical Addition; L. Polymerization; M. Miscellaneous Reactions; References; II. Acylbenzofurans; 1. Formylbenzofurans; 2. Acylbenzofurans; 3. Miscellaneous reactions; A. Reduction; B. Oxidation
C. Alkaline DegradationD. Rearrangement of Acylbenzofuran Oximes; E. Rearrangement (Migration) in Acylbenzofurans; F. Willgerodt-Kindler Reaction; G. Wittig Reaction; H. Miscellaneous; References; III. Benzofurancarboxylic acids; 1. Benzofuran monocarboxylic Acids; A. 2-Benzofurancarboxylic Acids; B. 3-Benzofurancarboxylic Acids; C. Hydroxybenzofurancarboxylic Acids; 2. Benzofuran Dicarboxylic Acids; 3. Benzofuranylalkanoic Acids; A. Benzofuranylacetic Acids; B. Benzofuranylpropionic Acids; C. Benzofuranylbutyric Acids; D. Miscellaneous Benzofuranylalkanoic Acids
4. Miscellaneous Reactions of Benzofurancarboxylic AcidsA. Halogenation; B. Chloromethylation; C. Nitration; D. Saponification; E. Catalytic Hydrogenation; F. Peroxide Formation and Ozonolysis; G. Acylation; H. Alkylation; I. Miscellaneous Reactions; References; IV. Hydrogenated Benzofurans; 1. Dihydrobenzofurans; A. Alkyl- (or Aryl-) Substituted 2.3-Dihydrobenzofurans; B. Halogen-Substituted 2,3-Dihydrobenzofurans; C. Nitro-Substituted 2,3-Dihydrobenzofurans; D. Amino-Substituted 2,3-Dihydrobenzofurans; E. 2.3-Dihydrobenzofuranols; F. Geometrical Isomers of 2,3-Dihydrobenzofurans
G. Miscellaneous Reactions of 2,3-Dihydrobenzofurans
Record Nr. UNINA-9910642680003321
Mustafa Ahmed <1918->  
New York, : Wiley, 1974
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Benzofurans [[electronic resource]]
Benzofurans [[electronic resource]]
Autore Mustafa Ahmed <1918->
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Wiley, 1974
Descrizione fisica 1 online resource (538 p.)
Disciplina 547.592
547/.59/05
547/.592
Collana The Chemistry of heterocyclic compounds
Soggetto topico Benzofuran - lemac
Heterocyclic compounds
ISBN 1-282-30174-8
9786612301742
0-470-18699-2
0-470-18850-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Matter; Preface; Contents; I. Benzofurans; 1. Introduction and Nomenclature; 2. Benzofuran and Its Alkyl Derivatives; A. Preparation; a. Catalytic Dehydrocyclization; b. Cyclizution of Allylphenols; c. Cyclodehydration of Ary foxy ketones; d. Rearrangement of' O-Aryloximes; e. Dehydrogenation of Bz-AIkyldihydrobenzofurans; f. Reduction of 2-Acetonyl-o-benzoquinols; g. Hydrogenation of 2-Acetylbenzofuran; h. Reaction of Copper Acetylides with Aryl Halides; i. Decarboxylation of Benzofurancarboxylic Acids; j. Photochemical Formation of Benzofurans; k. Adsorptive Cyclization
l. Condensation of Methylene Bis (ethyl sulfone)with Salicylaldehydes3. Aryl benzofurans; A. Preparation; a. Cychdehydration of w-Arloxyacetophenones; b. Condensation of Benzoins with Phenols; c. 1,3-Dipolar Additions of Oxocarbenes; d. Copper-Catalyzed Decomposition of Diazoketones; e. Ethynation of P-Benzoquinone; f Oxidation of Flavylium and Pyrylium Salts; g. Algar-Flynn-Oyamada Oxidation of 2'-Hydroxychalcones; h. Acid-Catalyzed Cyclization of O-Aryloximes; i. Photolytic Cyclizalions.; j. Miscellaneous; 4. Halobenzofurans; A. Caloro Derivatives; B. Bromo Derivatives; C. Iodo Derivatives
D. Fluoro Derivatives5. Nitrobenzofurans; 6. Benzofuranols; 7. Aminobenzofurans; 8. Benzofuranquinones; 9. Miscellaneous Reactions and Properties; A. Catalytic Hydrogenation; B. Oxidation; C. Ozonolysis; D. Nitration; E. Halogenation; F. Benzofuranylmetallic Compounds; G. Friedel-Crafts Techniques; H. Hoesch and Gatterman Techniques; I. With Diazoalkanes; J. With Dihalocarbene; K. Cyclophotochemical Addition; L. Polymerization; M. Miscellaneous Reactions; References; II. Acylbenzofurans; 1. Formylbenzofurans; 2. Acylbenzofurans; 3. Miscellaneous reactions; A. Reduction; B. Oxidation
C. Alkaline DegradationD. Rearrangement of Acylbenzofuran Oximes; E. Rearrangement (Migration) in Acylbenzofurans; F. Willgerodt-Kindler Reaction; G. Wittig Reaction; H. Miscellaneous; References; III. Benzofurancarboxylic acids; 1. Benzofuran monocarboxylic Acids; A. 2-Benzofurancarboxylic Acids; B. 3-Benzofurancarboxylic Acids; C. Hydroxybenzofurancarboxylic Acids; 2. Benzofuran Dicarboxylic Acids; 3. Benzofuranylalkanoic Acids; A. Benzofuranylacetic Acids; B. Benzofuranylpropionic Acids; C. Benzofuranylbutyric Acids; D. Miscellaneous Benzofuranylalkanoic Acids
4. Miscellaneous Reactions of Benzofurancarboxylic AcidsA. Halogenation; B. Chloromethylation; C. Nitration; D. Saponification; E. Catalytic Hydrogenation; F. Peroxide Formation and Ozonolysis; G. Acylation; H. Alkylation; I. Miscellaneous Reactions; References; IV. Hydrogenated Benzofurans; 1. Dihydrobenzofurans; A. Alkyl- (or Aryl-) Substituted 2.3-Dihydrobenzofurans; B. Halogen-Substituted 2,3-Dihydrobenzofurans; C. Nitro-Substituted 2,3-Dihydrobenzofurans; D. Amino-Substituted 2,3-Dihydrobenzofurans; E. 2.3-Dihydrobenzofuranols; F. Geometrical Isomers of 2,3-Dihydrobenzofurans
G. Miscellaneous Reactions of 2,3-Dihydrobenzofurans
Record Nr. UNINA-9910830944703321
Mustafa Ahmed <1918->  
New York, : Wiley, 1974
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Benzofurans
Benzofurans
Autore Mustafa Ahmed <1918->
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Wiley, 1974
Descrizione fisica 1 online resource (538 p.)
Disciplina 547.592
547/.59/05
547/.592
Collana The Chemistry of heterocyclic compounds
Soggetto topico Benzofuran
Heterocyclic compounds
ISBN 1-282-30174-8
9786612301742
0-470-18699-2
0-470-18850-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Matter; Preface; Contents; I. Benzofurans; 1. Introduction and Nomenclature; 2. Benzofuran and Its Alkyl Derivatives; A. Preparation; a. Catalytic Dehydrocyclization; b. Cyclizution of Allylphenols; c. Cyclodehydration of Ary foxy ketones; d. Rearrangement of' O-Aryloximes; e. Dehydrogenation of Bz-AIkyldihydrobenzofurans; f. Reduction of 2-Acetonyl-o-benzoquinols; g. Hydrogenation of 2-Acetylbenzofuran; h. Reaction of Copper Acetylides with Aryl Halides; i. Decarboxylation of Benzofurancarboxylic Acids; j. Photochemical Formation of Benzofurans; k. Adsorptive Cyclization
l. Condensation of Methylene Bis (ethyl sulfone)with Salicylaldehydes3. Aryl benzofurans; A. Preparation; a. Cychdehydration of w-Arloxyacetophenones; b. Condensation of Benzoins with Phenols; c. 1,3-Dipolar Additions of Oxocarbenes; d. Copper-Catalyzed Decomposition of Diazoketones; e. Ethynation of P-Benzoquinone; f Oxidation of Flavylium and Pyrylium Salts; g. Algar-Flynn-Oyamada Oxidation of 2'-Hydroxychalcones; h. Acid-Catalyzed Cyclization of O-Aryloximes; i. Photolytic Cyclizalions.; j. Miscellaneous; 4. Halobenzofurans; A. Caloro Derivatives; B. Bromo Derivatives; C. Iodo Derivatives
D. Fluoro Derivatives5. Nitrobenzofurans; 6. Benzofuranols; 7. Aminobenzofurans; 8. Benzofuranquinones; 9. Miscellaneous Reactions and Properties; A. Catalytic Hydrogenation; B. Oxidation; C. Ozonolysis; D. Nitration; E. Halogenation; F. Benzofuranylmetallic Compounds; G. Friedel-Crafts Techniques; H. Hoesch and Gatterman Techniques; I. With Diazoalkanes; J. With Dihalocarbene; K. Cyclophotochemical Addition; L. Polymerization; M. Miscellaneous Reactions; References; II. Acylbenzofurans; 1. Formylbenzofurans; 2. Acylbenzofurans; 3. Miscellaneous reactions; A. Reduction; B. Oxidation
C. Alkaline DegradationD. Rearrangement of Acylbenzofuran Oximes; E. Rearrangement (Migration) in Acylbenzofurans; F. Willgerodt-Kindler Reaction; G. Wittig Reaction; H. Miscellaneous; References; III. Benzofurancarboxylic acids; 1. Benzofuran monocarboxylic Acids; A. 2-Benzofurancarboxylic Acids; B. 3-Benzofurancarboxylic Acids; C. Hydroxybenzofurancarboxylic Acids; 2. Benzofuran Dicarboxylic Acids; 3. Benzofuranylalkanoic Acids; A. Benzofuranylacetic Acids; B. Benzofuranylpropionic Acids; C. Benzofuranylbutyric Acids; D. Miscellaneous Benzofuranylalkanoic Acids
4. Miscellaneous Reactions of Benzofurancarboxylic AcidsA. Halogenation; B. Chloromethylation; C. Nitration; D. Saponification; E. Catalytic Hydrogenation; F. Peroxide Formation and Ozonolysis; G. Acylation; H. Alkylation; I. Miscellaneous Reactions; References; IV. Hydrogenated Benzofurans; 1. Dihydrobenzofurans; A. Alkyl- (or Aryl-) Substituted 2.3-Dihydrobenzofurans; B. Halogen-Substituted 2,3-Dihydrobenzofurans; C. Nitro-Substituted 2,3-Dihydrobenzofurans; D. Amino-Substituted 2,3-Dihydrobenzofurans; E. 2.3-Dihydrobenzofuranols; F. Geometrical Isomers of 2,3-Dihydrobenzofurans
G. Miscellaneous Reactions of 2,3-Dihydrobenzofurans
Record Nr. UNINA-9910877531703321
Mustafa Ahmed <1918->  
New York, : Wiley, 1974
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chromenes, chromanones, and chromones [[electronic resource] /] / edited by G. P. Ellis
Chromenes, chromanones, and chromones [[electronic resource] /] / edited by G. P. Ellis
Pubbl/distr/stampa New York, : Wiley, c1977
Descrizione fisica 1 online resource (1213 p.)
Disciplina 547.592
547/.59/05
547/.592
Altri autori (Persone) EllisG. P (Gwynn Pennant)
Collana Chemistry of heterocyclic compounds
Soggetto topico Benzopyrans
Chromenes
Chromones
Soggetto genere / forma Electronic books.
ISBN 1-282-30176-4
9786612301766
0-470-18701-8
0-470-18852-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CHROMENES, CHROMANONES, AND CHROMONES; Contents; I. Chromenes, Chromanones, and Chromones-Introduction; II. 2H- and 4H-1-Benzopyrans; Ill. 3- and 4-Chromanols; IV. 3-Chromanones; V. 4-Chromanones; VI. 2,4-Chromandiones and 2,3,4-Chromantriones; VII. Naturally Occurring Chromones; VIII. Analytical Aspects of Chromones; IX. General Methods of Preparing Chromones; X. Chromone and Its Benzo Derivatives; XI. Alkylchromones; XII. Hydroxychromones; XIII. Alkoxychromones; XIV. Halochromones; XV. Nitrochromones; XVI. Aminochromones; XVII. Ketonic Chromones
XVIII. Chromone Carbonitriles and Tetrazole DerivativesXIX. C hromone Carboxaldehydes; XX. Chromone Carboxylic Acids and Their Derivatives; XXI. Bischromones and Bichromones; Author Index; Subject Index
Record Nr. UNINA-9910144280403321
New York, : Wiley, c1977
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chromenes, chromanones, and chromones [[electronic resource] /] / edited by G. P. Ellis
Chromenes, chromanones, and chromones [[electronic resource] /] / edited by G. P. Ellis
Pubbl/distr/stampa New York, : Wiley, c1977
Descrizione fisica 1 online resource (1213 p.)
Disciplina 547.592
547/.59/05
547/.592
Altri autori (Persone) EllisG. P (Gwynn Pennant)
Collana Chemistry of heterocyclic compounds
Soggetto topico Benzopyrans
Chromenes
Chromones
ISBN 1-282-30176-4
9786612301766
0-470-18701-8
0-470-18852-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CHROMENES, CHROMANONES, AND CHROMONES; Contents; I. Chromenes, Chromanones, and Chromones-Introduction; II. 2H- and 4H-1-Benzopyrans; Ill. 3- and 4-Chromanols; IV. 3-Chromanones; V. 4-Chromanones; VI. 2,4-Chromandiones and 2,3,4-Chromantriones; VII. Naturally Occurring Chromones; VIII. Analytical Aspects of Chromones; IX. General Methods of Preparing Chromones; X. Chromone and Its Benzo Derivatives; XI. Alkylchromones; XII. Hydroxychromones; XIII. Alkoxychromones; XIV. Halochromones; XV. Nitrochromones; XVI. Aminochromones; XVII. Ketonic Chromones
XVIII. Chromone Carbonitriles and Tetrazole DerivativesXIX. C hromone Carboxaldehydes; XX. Chromone Carboxylic Acids and Their Derivatives; XXI. Bischromones and Bichromones; Author Index; Subject Index
Record Nr. UNINA-9910643039903321
New York, : Wiley, c1977
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chromenes, chromanones, and chromones [[electronic resource] /] / edited by G. P. Ellis
Chromenes, chromanones, and chromones [[electronic resource] /] / edited by G. P. Ellis
Pubbl/distr/stampa New York, : Wiley, c1977
Descrizione fisica 1 online resource (1213 p.)
Disciplina 547.592
547/.59/05
547/.592
Altri autori (Persone) EllisG. P (Gwynn Pennant)
Collana Chemistry of heterocyclic compounds
Soggetto topico Benzopyrans
Chromenes
Chromones
ISBN 1-282-30176-4
9786612301766
0-470-18701-8
0-470-18852-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CHROMENES, CHROMANONES, AND CHROMONES; Contents; I. Chromenes, Chromanones, and Chromones-Introduction; II. 2H- and 4H-1-Benzopyrans; Ill. 3- and 4-Chromanols; IV. 3-Chromanones; V. 4-Chromanones; VI. 2,4-Chromandiones and 2,3,4-Chromantriones; VII. Naturally Occurring Chromones; VIII. Analytical Aspects of Chromones; IX. General Methods of Preparing Chromones; X. Chromone and Its Benzo Derivatives; XI. Alkylchromones; XII. Hydroxychromones; XIII. Alkoxychromones; XIV. Halochromones; XV. Nitrochromones; XVI. Aminochromones; XVII. Ketonic Chromones
XVIII. Chromone Carbonitriles and Tetrazole DerivativesXIX. C hromone Carboxaldehydes; XX. Chromone Carboxylic Acids and Their Derivatives; XXI. Bischromones and Bichromones; Author Index; Subject Index
Record Nr. UNINA-9910830430303321
New York, : Wiley, c1977
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chromenes, chromanones, and chromones / / edited by G. P. Ellis
Chromenes, chromanones, and chromones / / edited by G. P. Ellis
Pubbl/distr/stampa New York, : Wiley, c1977
Descrizione fisica 1 online resource (1213 p.)
Disciplina 547.592
547/.59/05
547/.592
Altri autori (Persone) EllisG. P (Gwynn Pennant)
Collana Chemistry of heterocyclic compounds
Soggetto topico Benzopyrans
Chromans
Chromone
ISBN 1-282-30176-4
9786612301766
0-470-18701-8
0-470-18852-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CHROMENES, CHROMANONES, AND CHROMONES; Contents; I. Chromenes, Chromanones, and Chromones-Introduction; II. 2H- and 4H-1-Benzopyrans; Ill. 3- and 4-Chromanols; IV. 3-Chromanones; V. 4-Chromanones; VI. 2,4-Chromandiones and 2,3,4-Chromantriones; VII. Naturally Occurring Chromones; VIII. Analytical Aspects of Chromones; IX. General Methods of Preparing Chromones; X. Chromone and Its Benzo Derivatives; XI. Alkylchromones; XII. Hydroxychromones; XIII. Alkoxychromones; XIV. Halochromones; XV. Nitrochromones; XVI. Aminochromones; XVII. Ketonic Chromones
XVIII. Chromone Carbonitriles and Tetrazole DerivativesXIX. C hromone Carboxaldehydes; XX. Chromone Carboxylic Acids and Their Derivatives; XXI. Bischromones and Bichromones; Author Index; Subject Index
Record Nr. UNINA-9910876803703321
New York, : Wiley, c1977
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Isoxazoles . Part two / / edited by Paolo Grunanger, Paola Vita-Finzi; developmental editing by James E. Dowling
Isoxazoles . Part two / / edited by Paolo Grunanger, Paola Vita-Finzi; developmental editing by James E. Dowling
Autore Grunanger Paolo
Pubbl/distr/stampa New York, : John Wiley & Sons, 1999
Descrizione fisica 1 online resource (905 p.)
Disciplina 547.592
547/.59/05
547/.592
Altri autori (Persone) Vita-FinziPaola
DowlingJames Edward <1966->
Collana Chemistry of heterocyclic compounds
Soggetto topico Oxazoles
Chemistry
ISBN 1-282-30715-0
9786612307157
0-470-18736-0
0-470-18888-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto ISOXAZOLES; Contents; 1 1,2 BENZISOXALES; 2 2,1-BENZISOXAZOLES; 3 HETEROCYCLES CONDENSED TO THE ISOXAZOLE RING; 4 PARTIALLY SATURATED POLYNUCLEAR ISOXAZOLES; INDEX
Record Nr. UNINA-9910876803603321
Grunanger Paolo  
New York, : John Wiley & Sons, 1999
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Isoxazoles . Part one / / Paolo Grunanger, Paola Vita-Finzi
Isoxazoles . Part one / / Paolo Grunanger, Paola Vita-Finzi
Autore Grunanger Paolo
Pubbl/distr/stampa New York, : John Wiley & Sons, 1991
Descrizione fisica 1 online resource (904 p.)
Disciplina 547.592
547/.59/05
547/.592
Altri autori (Persone) Vita-FinziPaola
DowlingJames Edward <1966->
Collana Chemistry of heterocyclic compounds
Soggetto topico Oxazoles
Chemistry
ISBN 1-282-30723-1
9786612307232
0-470-18735-2
0-470-18887-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto ISOXAZOLES; The Chemistry of Heterocyclic Compounds Introduction to the Series; Preface; Contents; CHAPTER 1; 1. Isoxazoles; 1.1 Introduction; 1.2 Physicochemical Properties; 1.2.1 Infrared Spectra; 1.2.2 Ultraviolet Spectra; 1.2.3 Nuclear Magnetic Resonance Spectra; 1.2.3.1 PMR Spectra; 1.2.3.2 I3C-NMR Spectra; 1.2.3.3 I4N- and ""N-NMR Spectra; 1.2.3.4 Other Nuclei NMR Spectra; 1.2.4 Mass Spectra; 1.2.5 Other Spectra; 1.2.5.1 Microwave Spectra; 1.2.5.2 Photoelectron Spectra; 1.2.5.3 Electron Paramagnetic Resonance Spectra; 1.2.5.4 Electron Spin Resonance Spectra
1.2.5.5 Nuclear Quadrupole Resonance Spectra1.2.5.6 Other Spectra; 1.2.6 Crystal and Molecular Structure; 1.2.7 Dipole Moments; 1.2.8 Theoretical Calculations; 1.2.8.1 Reactivity, Aromaticity, and Electron Density; 1.2.8.2 Molecular Geometry; 1.2.8.3 Basicity and Dipole Moments; 1.2.8.4 Ionization Potentials; 1.2.8.5 Molecular Core Binding Energy; 1.2.8.6 Spectroscopic Data and Conformational Analysis; 1.2.9 Basicity; 1.2.10 Miscellaneous Data; 1.2.11 Analytical Methods; 1.3 Methods of Preparation; 1.3.1 [CCC + NO] Processes; 1.3.1.1 Oximation of 1, 3-Dicarbonyl (and Related) Compounds
1.3.1.2 Oximation of a-Acetylenic Carbonyl (and Related) Compounds1.3.1.3 Oximation of a-Dihalocarbonyl (and Related) Compounds; 1.3.1.4 Oximation of z, 8-Ethylenic Carbonyl (and Related) Compounds 8-Substituted with Electron-Withdrawing Groups; 1.3.1.5 Oximation of a, b-Ethylenic Carbonyl (and Related) Compounds; 1.3.1.6 Other Oximation Reactions; 1.3.1.7 Synthesis from Unsaturated Compounds and Nitric (Nitrous) Acid; 1.3.1.8 Nitrosation of Ketodicarboxylic Esters; 1.3.2 [CNO + CC] Processes; 1.3.2.1 Cycloaddition of Nitrile Oxides (or Their Precursors) to Acetylenic Compounds
1.3.2.2 Cycloaddition of Nitrile Oxides (or Their Precursors) to Ethylenic Compounds1.3.2.3 Cycloaddition of Nitrile Oxides (or Their Precursors) with Active Methylene Compounds; 1.3.2.4 Cycloaddition of Nitrile Oxides (or Their Precursors) with Sodium Acetylides or Acetylenic Grignard Reagents; 1.3.2.5 Other [CNO + CC] Processes; 1.3.3 [CNO + 2C] Processes: Syntheses from Nitro Derivatives; 1.3.4 [CCNO + C] Processes; 1.3.4.1 Synthesis from Oxime Dilithium Salts and Carboxylic Acid Derivatives; 1.3.4.2 Reaction of a-Chloroketoximes with Ylides; 1.3.5 [CCCN + O] Process
1.3.6 Cyclization Processes1.3.6.1 [OCCCN] Processes; 1.3.6.2 [CCCON] Processes; 1.3.6.3 [CCNOC] Processes; 1.3.6.4 [CCCNO] Processes; 1.3.7 From Heterocyclic Compounds; 1.3.7.1 From Other 1, 2-Oxazole Derivatives; 1.3.7.2 From Other Heterocycles; 1.4 Chemical Properties; 1.4.1 Protonation and Quaternization; 1.4.2 Complexation; 1.4.2.1 Metallic Complexes; 1.4.2.2 Molecular Complexes; 1.4.3 Reduction Reactions; 1.4.3.1 Hydrogenolytic Ring Cleavage; 1.4.3.2 Reductions without Ring Cleavage; 1.4.4 Oxidation Reactions; 1.4.5 Thermolysis and Photolysis; 1.4.6 Reactions with Nucleophiles
1.4.6.1 Reactions with Ring Cleavage
Record Nr. UNINA-9910877238203321
Grunanger Paolo  
New York, : John Wiley & Sons, 1991
Materiale a stampa
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