top

  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.

  Info

  • Utilizzare questo link per rimuovere la selezione effettuata.
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
Furopyrans and furopyrones [[electronic resource] /] / Ahmed Mustafa
Furopyrans and furopyrones [[electronic resource] /] / Ahmed Mustafa
Autore Mustafa Ahmed <1918->
Edizione [99th ed.]
Pubbl/distr/stampa London ; ; New York, : Interscience Publishers, 1967
Descrizione fisica 1 online resource (391 p.)
Disciplina 547/.59/05
Collana The chemistry of heterocyclic compounds
Soggetto topico Furopyran
Furopyranone
Soggetto genere / forma Electronic books.
ISBN 1-282-30163-2
9786612301636
0-470-18687-9
0-470-18835-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUROPYRANS and FUROPYRONES; Contents; I. Fumpyrans and -pyronea; I. Naturally Occurring Furopyrms; 1. Plumericin; 2. Anhydrotetrahydroaucubigenin; II. Synthetic Furopyrans and -pyrones; III. References; II. Furocoumorins; I. Isolation; II. Physical Properties; III. Nomenclature; IV. Naturally Occurring Furocoumarins; 1. Structure and Chemicd Properties; A. Angelicin; B. Psoralen; C. Bergapten; D. Bergaptol; E. Isobergapten.; F. Bergamuttin.; G. Xanthotoxin; H. Xanthotoxol; I. Isoimperetorin; J. Oxypeucedanin; K. ostruthol; L. Imperstorin; M. Alloimperatorin; N. Herdenin; O. Isopimpinellin
P. PhellopterinQ. Byekangelicol; R. Byakangelicin; S. Pimpinellin; T. Sphondin; U. Halfordin and Isohalfordm; V. Nodakenetin.; W. Peucedanin; X. Athamantin; Y. Discophoridin; Z. Edultin; AA.Peulustrin; BB. Columbiansdin and Columbisnin; CC. Archangelicin; DD. Archangelin; EE. Pyrocanescin; FF. 4,5',8-Trimethylpralen; GG. Aflatoxins B and G; 2. Configuration; 3. Biosynthesia; A. a-(B'-Hydroxypropyl)dihydrofurans and a-Lsopropenyl-dihydrofurans; B. a-Isopropyl-B--hydroxyfurans and Relations; C. Simple Furans; 4. Physiological Activity; V. References; III. Furochromones; I. Isolation
II. Physical PropertiesIII. Nomenclature; IV. Naturally Occurring Furochromones; 1. Chemical Properties; A. Khellin; (1) synthesis of khellin; (2) Synthesis of khellin analogs; (3) Reactions; B. Visnagin; (1) synthesis of visnagin; (2) Syntheeis of visnagin analogs and related transformations; (3) Reactions; C. Khellinol; D.Khellinin; E. Khellol; F. Anamiol; G. Visanminol; 2. Color Reactions; 3. Physiological Activity; V. References; IV.Furoxanthones; I. Naturally Occurring Furoxanthones; 1. Sterigmatocystin; II. Synthetic Furoxanthones; III. References; V. Furoflavones; I. Isolation
II. Physical PropertiesIII. Naturdy Occurring Furoflavones; 1. chemical Properties; A. Karanjin; B. Lanceolatin B; C. Pongapin; D. Kenjone; E. Pongaglabrone; F.Atanasin; G. Gamatin; H. Pinnatin; IV. Synthetic Furoflavones; 1. Linear-type; 2. Angular-type; V. References; VI. Furoisoflavanoids; I. Introduction; II. Furoisoflavanones; 1. Naturally Occurring Furoisoflavenones; A. Nepseudin; B. Neotenone; 2. Synthetic Fuarioflavanones; A. Angular Furoisoflavones; (1) Introduction of a furan nucleus into an isoflavone skeleton (Tanaka's method); (2) Ethyl orthoformate method (Venkataraman)
B. Linear Furo(3"",2""-6,7)isoflavonesIII. Coumaranochromans; 1. Introduction; 2. Naturally Occurring Coumaranochromans; A. Homopterocarpin; B. Pterocarpin; C. Maackiain; D. Pisatin; E. Neodulin; F.Phaseollin; IV. Coumaronoflavan-4-ols; 1. NaturalIy Occurring Coumamnoflavan-4-ols; A. Cyanomaclurin; 2. Synthetic 11H-benzofuro(3,2-b)-1-benzopyran-11-ones; V. Coumaronocoumarins; 1. Naturally Occurring Coumaronocoumarins; A. Coumestrol; B. Wedelolactone; C. Trifoliol; D. Medicagol; E. Psoralidin; VI. 3-Arylfurocoumarins; VII. Coumaronofurocoumarins; VIII. Furo(3,2-c)-1-benzopyran-4-ones
IX. Physiological Activity
Record Nr. UNINA-9910144283303321
Mustafa Ahmed <1918->  
London ; ; New York, : Interscience Publishers, 1967
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Furopyrans and furopyrones [[electronic resource] /] / Ahmed Mustafa
Furopyrans and furopyrones [[electronic resource] /] / Ahmed Mustafa
Autore Mustafa Ahmed <1918->
Edizione [99th ed.]
Pubbl/distr/stampa London ; ; New York, : Interscience Publishers, 1967
Descrizione fisica 1 online resource (391 p.)
Disciplina 547/.59/05
Collana The chemistry of heterocyclic compounds
Soggetto topico Furopyran
Furopyranone
ISBN 1-282-30163-2
9786612301636
0-470-18687-9
0-470-18835-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUROPYRANS and FUROPYRONES; Contents; I. Fumpyrans and -pyronea; I. Naturally Occurring Furopyrms; 1. Plumericin; 2. Anhydrotetrahydroaucubigenin; II. Synthetic Furopyrans and -pyrones; III. References; II. Furocoumorins; I. Isolation; II. Physical Properties; III. Nomenclature; IV. Naturally Occurring Furocoumarins; 1. Structure and Chemicd Properties; A. Angelicin; B. Psoralen; C. Bergapten; D. Bergaptol; E. Isobergapten.; F. Bergamuttin.; G. Xanthotoxin; H. Xanthotoxol; I. Isoimperetorin; J. Oxypeucedanin; K. ostruthol; L. Imperstorin; M. Alloimperatorin; N. Herdenin; O. Isopimpinellin
P. PhellopterinQ. Byekangelicol; R. Byakangelicin; S. Pimpinellin; T. Sphondin; U. Halfordin and Isohalfordm; V. Nodakenetin.; W. Peucedanin; X. Athamantin; Y. Discophoridin; Z. Edultin; AA.Peulustrin; BB. Columbiansdin and Columbisnin; CC. Archangelicin; DD. Archangelin; EE. Pyrocanescin; FF. 4,5',8-Trimethylpralen; GG. Aflatoxins B and G; 2. Configuration; 3. Biosynthesia; A. a-(B'-Hydroxypropyl)dihydrofurans and a-Lsopropenyl-dihydrofurans; B. a-Isopropyl-B--hydroxyfurans and Relations; C. Simple Furans; 4. Physiological Activity; V. References; III. Furochromones; I. Isolation
II. Physical PropertiesIII. Nomenclature; IV. Naturally Occurring Furochromones; 1. Chemical Properties; A. Khellin; (1) synthesis of khellin; (2) Synthesis of khellin analogs; (3) Reactions; B. Visnagin; (1) synthesis of visnagin; (2) Syntheeis of visnagin analogs and related transformations; (3) Reactions; C. Khellinol; D.Khellinin; E. Khellol; F. Anamiol; G. Visanminol; 2. Color Reactions; 3. Physiological Activity; V. References; IV.Furoxanthones; I. Naturally Occurring Furoxanthones; 1. Sterigmatocystin; II. Synthetic Furoxanthones; III. References; V. Furoflavones; I. Isolation
II. Physical PropertiesIII. Naturdy Occurring Furoflavones; 1. chemical Properties; A. Karanjin; B. Lanceolatin B; C. Pongapin; D. Kenjone; E. Pongaglabrone; F.Atanasin; G. Gamatin; H. Pinnatin; IV. Synthetic Furoflavones; 1. Linear-type; 2. Angular-type; V. References; VI. Furoisoflavanoids; I. Introduction; II. Furoisoflavanones; 1. Naturally Occurring Furoisoflavenones; A. Nepseudin; B. Neotenone; 2. Synthetic Fuarioflavanones; A. Angular Furoisoflavones; (1) Introduction of a furan nucleus into an isoflavone skeleton (Tanaka's method); (2) Ethyl orthoformate method (Venkataraman)
B. Linear Furo(3"",2""-6,7)isoflavonesIII. Coumaranochromans; 1. Introduction; 2. Naturally Occurring Coumaranochromans; A. Homopterocarpin; B. Pterocarpin; C. Maackiain; D. Pisatin; E. Neodulin; F.Phaseollin; IV. Coumaronoflavan-4-ols; 1. NaturalIy Occurring Coumamnoflavan-4-ols; A. Cyanomaclurin; 2. Synthetic 11H-benzofuro(3,2-b)-1-benzopyran-11-ones; V. Coumaronocoumarins; 1. Naturally Occurring Coumaronocoumarins; A. Coumestrol; B. Wedelolactone; C. Trifoliol; D. Medicagol; E. Psoralidin; VI. 3-Arylfurocoumarins; VII. Coumaronofurocoumarins; VIII. Furo(3,2-c)-1-benzopyran-4-ones
IX. Physiological Activity
Record Nr. UNINA-9910642621003321
Mustafa Ahmed <1918->  
London ; ; New York, : Interscience Publishers, 1967
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Furopyrans and furopyrones [[electronic resource] /] / Ahmed Mustafa
Furopyrans and furopyrones [[electronic resource] /] / Ahmed Mustafa
Autore Mustafa Ahmed <1918->
Edizione [99th ed.]
Pubbl/distr/stampa London ; ; New York, : Interscience Publishers, 1967
Descrizione fisica 1 online resource (391 p.)
Disciplina 547/.59/05
Collana The chemistry of heterocyclic compounds
Soggetto topico Furopyran
Furopyranone
ISBN 1-282-30163-2
9786612301636
0-470-18687-9
0-470-18835-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUROPYRANS and FUROPYRONES; Contents; I. Fumpyrans and -pyronea; I. Naturally Occurring Furopyrms; 1. Plumericin; 2. Anhydrotetrahydroaucubigenin; II. Synthetic Furopyrans and -pyrones; III. References; II. Furocoumorins; I. Isolation; II. Physical Properties; III. Nomenclature; IV. Naturally Occurring Furocoumarins; 1. Structure and Chemicd Properties; A. Angelicin; B. Psoralen; C. Bergapten; D. Bergaptol; E. Isobergapten.; F. Bergamuttin.; G. Xanthotoxin; H. Xanthotoxol; I. Isoimperetorin; J. Oxypeucedanin; K. ostruthol; L. Imperstorin; M. Alloimperatorin; N. Herdenin; O. Isopimpinellin
P. PhellopterinQ. Byekangelicol; R. Byakangelicin; S. Pimpinellin; T. Sphondin; U. Halfordin and Isohalfordm; V. Nodakenetin.; W. Peucedanin; X. Athamantin; Y. Discophoridin; Z. Edultin; AA.Peulustrin; BB. Columbiansdin and Columbisnin; CC. Archangelicin; DD. Archangelin; EE. Pyrocanescin; FF. 4,5',8-Trimethylpralen; GG. Aflatoxins B and G; 2. Configuration; 3. Biosynthesia; A. a-(B'-Hydroxypropyl)dihydrofurans and a-Lsopropenyl-dihydrofurans; B. a-Isopropyl-B--hydroxyfurans and Relations; C. Simple Furans; 4. Physiological Activity; V. References; III. Furochromones; I. Isolation
II. Physical PropertiesIII. Nomenclature; IV. Naturally Occurring Furochromones; 1. Chemical Properties; A. Khellin; (1) synthesis of khellin; (2) Synthesis of khellin analogs; (3) Reactions; B. Visnagin; (1) synthesis of visnagin; (2) Syntheeis of visnagin analogs and related transformations; (3) Reactions; C. Khellinol; D.Khellinin; E. Khellol; F. Anamiol; G. Visanminol; 2. Color Reactions; 3. Physiological Activity; V. References; IV.Furoxanthones; I. Naturally Occurring Furoxanthones; 1. Sterigmatocystin; II. Synthetic Furoxanthones; III. References; V. Furoflavones; I. Isolation
II. Physical PropertiesIII. Naturdy Occurring Furoflavones; 1. chemical Properties; A. Karanjin; B. Lanceolatin B; C. Pongapin; D. Kenjone; E. Pongaglabrone; F.Atanasin; G. Gamatin; H. Pinnatin; IV. Synthetic Furoflavones; 1. Linear-type; 2. Angular-type; V. References; VI. Furoisoflavanoids; I. Introduction; II. Furoisoflavanones; 1. Naturally Occurring Furoisoflavenones; A. Nepseudin; B. Neotenone; 2. Synthetic Fuarioflavanones; A. Angular Furoisoflavones; (1) Introduction of a furan nucleus into an isoflavone skeleton (Tanaka's method); (2) Ethyl orthoformate method (Venkataraman)
B. Linear Furo(3"",2""-6,7)isoflavonesIII. Coumaranochromans; 1. Introduction; 2. Naturally Occurring Coumaranochromans; A. Homopterocarpin; B. Pterocarpin; C. Maackiain; D. Pisatin; E. Neodulin; F.Phaseollin; IV. Coumaronoflavan-4-ols; 1. NaturalIy Occurring Coumamnoflavan-4-ols; A. Cyanomaclurin; 2. Synthetic 11H-benzofuro(3,2-b)-1-benzopyran-11-ones; V. Coumaronocoumarins; 1. Naturally Occurring Coumaronocoumarins; A. Coumestrol; B. Wedelolactone; C. Trifoliol; D. Medicagol; E. Psoralidin; VI. 3-Arylfurocoumarins; VII. Coumaronofurocoumarins; VIII. Furo(3,2-c)-1-benzopyran-4-ones
IX. Physiological Activity
Record Nr. UNISA-996202927003316
Mustafa Ahmed <1918->  
London ; ; New York, : Interscience Publishers, 1967
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Furopyrans and furopyrones [[electronic resource] /] / Ahmed Mustafa
Furopyrans and furopyrones [[electronic resource] /] / Ahmed Mustafa
Autore Mustafa Ahmed <1918->
Edizione [99th ed.]
Pubbl/distr/stampa London ; ; New York, : Interscience Publishers, 1967
Descrizione fisica 1 online resource (391 p.)
Disciplina 547/.59/05
Collana The chemistry of heterocyclic compounds
Soggetto topico Furopyran
Furopyranone
ISBN 1-282-30163-2
9786612301636
0-470-18687-9
0-470-18835-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUROPYRANS and FUROPYRONES; Contents; I. Fumpyrans and -pyronea; I. Naturally Occurring Furopyrms; 1. Plumericin; 2. Anhydrotetrahydroaucubigenin; II. Synthetic Furopyrans and -pyrones; III. References; II. Furocoumorins; I. Isolation; II. Physical Properties; III. Nomenclature; IV. Naturally Occurring Furocoumarins; 1. Structure and Chemicd Properties; A. Angelicin; B. Psoralen; C. Bergapten; D. Bergaptol; E. Isobergapten.; F. Bergamuttin.; G. Xanthotoxin; H. Xanthotoxol; I. Isoimperetorin; J. Oxypeucedanin; K. ostruthol; L. Imperstorin; M. Alloimperatorin; N. Herdenin; O. Isopimpinellin
P. PhellopterinQ. Byekangelicol; R. Byakangelicin; S. Pimpinellin; T. Sphondin; U. Halfordin and Isohalfordm; V. Nodakenetin.; W. Peucedanin; X. Athamantin; Y. Discophoridin; Z. Edultin; AA.Peulustrin; BB. Columbiansdin and Columbisnin; CC. Archangelicin; DD. Archangelin; EE. Pyrocanescin; FF. 4,5',8-Trimethylpralen; GG. Aflatoxins B and G; 2. Configuration; 3. Biosynthesia; A. a-(B'-Hydroxypropyl)dihydrofurans and a-Lsopropenyl-dihydrofurans; B. a-Isopropyl-B--hydroxyfurans and Relations; C. Simple Furans; 4. Physiological Activity; V. References; III. Furochromones; I. Isolation
II. Physical PropertiesIII. Nomenclature; IV. Naturally Occurring Furochromones; 1. Chemical Properties; A. Khellin; (1) synthesis of khellin; (2) Synthesis of khellin analogs; (3) Reactions; B. Visnagin; (1) synthesis of visnagin; (2) Syntheeis of visnagin analogs and related transformations; (3) Reactions; C. Khellinol; D.Khellinin; E. Khellol; F. Anamiol; G. Visanminol; 2. Color Reactions; 3. Physiological Activity; V. References; IV.Furoxanthones; I. Naturally Occurring Furoxanthones; 1. Sterigmatocystin; II. Synthetic Furoxanthones; III. References; V. Furoflavones; I. Isolation
II. Physical PropertiesIII. Naturdy Occurring Furoflavones; 1. chemical Properties; A. Karanjin; B. Lanceolatin B; C. Pongapin; D. Kenjone; E. Pongaglabrone; F.Atanasin; G. Gamatin; H. Pinnatin; IV. Synthetic Furoflavones; 1. Linear-type; 2. Angular-type; V. References; VI. Furoisoflavanoids; I. Introduction; II. Furoisoflavanones; 1. Naturally Occurring Furoisoflavenones; A. Nepseudin; B. Neotenone; 2. Synthetic Fuarioflavanones; A. Angular Furoisoflavones; (1) Introduction of a furan nucleus into an isoflavone skeleton (Tanaka's method); (2) Ethyl orthoformate method (Venkataraman)
B. Linear Furo(3"",2""-6,7)isoflavonesIII. Coumaranochromans; 1. Introduction; 2. Naturally Occurring Coumaranochromans; A. Homopterocarpin; B. Pterocarpin; C. Maackiain; D. Pisatin; E. Neodulin; F.Phaseollin; IV. Coumaronoflavan-4-ols; 1. NaturalIy Occurring Coumamnoflavan-4-ols; A. Cyanomaclurin; 2. Synthetic 11H-benzofuro(3,2-b)-1-benzopyran-11-ones; V. Coumaronocoumarins; 1. Naturally Occurring Coumaronocoumarins; A. Coumestrol; B. Wedelolactone; C. Trifoliol; D. Medicagol; E. Psoralidin; VI. 3-Arylfurocoumarins; VII. Coumaronofurocoumarins; VIII. Furo(3,2-c)-1-benzopyran-4-ones
IX. Physiological Activity
Record Nr. UNINA-9910830143703321
Mustafa Ahmed <1918->  
London ; ; New York, : Interscience Publishers, 1967
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Furopyrans and furopyrones / / Ahmed Mustafa
Furopyrans and furopyrones / / Ahmed Mustafa
Autore Mustafa Ahmed <1918->
Edizione [99th ed.]
Pubbl/distr/stampa London ; ; New York, : Interscience Publishers, 1967
Descrizione fisica 1 online resource (391 p.)
Disciplina 547/.59/05
Collana The chemistry of heterocyclic compounds
Soggetto topico Furopyran
Furopyranone
ISBN 1-282-30163-2
9786612301636
0-470-18687-9
0-470-18835-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUROPYRANS and FUROPYRONES; Contents; I. Fumpyrans and -pyronea; I. Naturally Occurring Furopyrms; 1. Plumericin; 2. Anhydrotetrahydroaucubigenin; II. Synthetic Furopyrans and -pyrones; III. References; II. Furocoumorins; I. Isolation; II. Physical Properties; III. Nomenclature; IV. Naturally Occurring Furocoumarins; 1. Structure and Chemicd Properties; A. Angelicin; B. Psoralen; C. Bergapten; D. Bergaptol; E. Isobergapten.; F. Bergamuttin.; G. Xanthotoxin; H. Xanthotoxol; I. Isoimperetorin; J. Oxypeucedanin; K. ostruthol; L. Imperstorin; M. Alloimperatorin; N. Herdenin; O. Isopimpinellin
P. PhellopterinQ. Byekangelicol; R. Byakangelicin; S. Pimpinellin; T. Sphondin; U. Halfordin and Isohalfordm; V. Nodakenetin.; W. Peucedanin; X. Athamantin; Y. Discophoridin; Z. Edultin; AA.Peulustrin; BB. Columbiansdin and Columbisnin; CC. Archangelicin; DD. Archangelin; EE. Pyrocanescin; FF. 4,5',8-Trimethylpralen; GG. Aflatoxins B and G; 2. Configuration; 3. Biosynthesia; A. a-(B'-Hydroxypropyl)dihydrofurans and a-Lsopropenyl-dihydrofurans; B. a-Isopropyl-B--hydroxyfurans and Relations; C. Simple Furans; 4. Physiological Activity; V. References; III. Furochromones; I. Isolation
II. Physical PropertiesIII. Nomenclature; IV. Naturally Occurring Furochromones; 1. Chemical Properties; A. Khellin; (1) synthesis of khellin; (2) Synthesis of khellin analogs; (3) Reactions; B. Visnagin; (1) synthesis of visnagin; (2) Syntheeis of visnagin analogs and related transformations; (3) Reactions; C. Khellinol; D.Khellinin; E. Khellol; F. Anamiol; G. Visanminol; 2. Color Reactions; 3. Physiological Activity; V. References; IV.Furoxanthones; I. Naturally Occurring Furoxanthones; 1. Sterigmatocystin; II. Synthetic Furoxanthones; III. References; V. Furoflavones; I. Isolation
II. Physical PropertiesIII. Naturdy Occurring Furoflavones; 1. chemical Properties; A. Karanjin; B. Lanceolatin B; C. Pongapin; D. Kenjone; E. Pongaglabrone; F.Atanasin; G. Gamatin; H. Pinnatin; IV. Synthetic Furoflavones; 1. Linear-type; 2. Angular-type; V. References; VI. Furoisoflavanoids; I. Introduction; II. Furoisoflavanones; 1. Naturally Occurring Furoisoflavenones; A. Nepseudin; B. Neotenone; 2. Synthetic Fuarioflavanones; A. Angular Furoisoflavones; (1) Introduction of a furan nucleus into an isoflavone skeleton (Tanaka's method); (2) Ethyl orthoformate method (Venkataraman)
B. Linear Furo(3"",2""-6,7)isoflavonesIII. Coumaranochromans; 1. Introduction; 2. Naturally Occurring Coumaranochromans; A. Homopterocarpin; B. Pterocarpin; C. Maackiain; D. Pisatin; E. Neodulin; F.Phaseollin; IV. Coumaronoflavan-4-ols; 1. NaturalIy Occurring Coumamnoflavan-4-ols; A. Cyanomaclurin; 2. Synthetic 11H-benzofuro(3,2-b)-1-benzopyran-11-ones; V. Coumaronocoumarins; 1. Naturally Occurring Coumaronocoumarins; A. Coumestrol; B. Wedelolactone; C. Trifoliol; D. Medicagol; E. Psoralidin; VI. 3-Arylfurocoumarins; VII. Coumaronofurocoumarins; VIII. Furo(3,2-c)-1-benzopyran-4-ones
IX. Physiological Activity
Record Nr. UNINA-9910876523903321
Mustafa Ahmed <1918->  
London ; ; New York, : Interscience Publishers, 1967
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui