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The chemistry of 1,2,3-Thiadiazoles [[electronic resource] /] / Vasiliy A. Bakulev, Wim Dehaen
The chemistry of 1,2,3-Thiadiazoles [[electronic resource] /] / Vasiliy A. Bakulev, Wim Dehaen
Autore Bakulev Vasiliy A
Pubbl/distr/stampa Hoboken, N.J., : John Wiley & Sons, c2004
Descrizione fisica 1 online resource (261 p.)
Disciplina 547.59
547.594
547/.59/05
Altri autori (Persone) DehaenW (Wim)
Collana The chemistry of heterocyclic compounds
Soggetto topico Thiadiazoles
Soggetto genere / forma Electronic books.
ISBN 1-280-54200-4
9786610542000
0-471-65699-2
0-471-65691-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE CHEMISTRY OF 1,2,3-THIADIAZOLES; The Chemistry of Heterocyclic Compounds Introduction to the Series; Preface; Acknowledgments; Contents; 1 Synthesis of 1,2,3-thiadiazoles; 1.1 Cyclization of Hydrazones with Thionyl Chloride (Hurd-Mori Synthesis); 1.1.1 Scope and Limitations; 1.1.2 Mechanism of the Hurd-Mori Reaction; 1.1.3 Application of the Hurd-Mori Reaction in Organic Synthesis; 1.2 Cycloaddition of Diazoalkanes onto a C=S bond (Pechmann Synthesis); 1.3 Heterocyclization of α-diazo Thiocarbonyl Compounds (Wolff Synthesis)
1.3.1 Introduction of a Diazo Function into Compounds Containing a C=S Bond1.3.2 Introduction of a C=S Bond in the α-position to a Diazo Group; 1.3.3 Simultaneous Introduction of Diazo and Thiocarbonyl Functions; 1.4 Transformations of other Sulfur-containing Heterocyclic Compounds; 1.5 Elaboration of Preformed 1,2,3-Thiadiazoles; 1.5.1 Carboxylic Acids; 1.5.2 Functional Derivatives of Carboxylic Acids; 1.5.3 Aldehydes; 1.5.4 Amino-1,2,3-Thiadiazoles; 1.5.5 Halo Derivatives; 1.5.6 5-Hydrazino-, 5-Mercapto-1,2,3-Thiadiazoles and 5-Sulfide Derivatives
1.5.7 2-(1,2,3-Thiadiazol-5-yl)acetic Acid Derivatives1.5.8 Alkenyl-1,2,3-Thiadiazoles; 1.5.9 5-Hydroxyiminomethyl- and 5-Diazomethyl-1,2,3-Thiadiazoles; 1.5.10 4-Hydroxymethyl-1,2,3-Thiadiazoles; 1.6 Tables; 1.7 Selected Procedures; 1.7.1 1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.2 4-Phenyl-1,2,3-Thiadiazole; 1.7.3 4-Phenyl-1,2,3-Thiadiazole-5-Carbaldehyde; 1.7.4 4-Phenyl-5-Oxyiminomethyl-1,2,3-Thiadiazole; 1.7.5 5-Phenyl-1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.6 5-Chloro-1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.7 Ethyl 5-amino-1,2,3-Thiadiazole-4-Carboxylate; 1.7.7.1 Pechmann Method
1.7.7.2 Wolff Method1.7.8 Ethyl 5-chloro-1,2,3-Thiadiazole-4-Carboxylate; 1.7.9 4-Phenyl-2-(2,4,6-Trichlorophenyl)-1,2,3-Thiadiazolium Chloride; 1.7.10 5-Amino-4-ethoxycarbonyl-2-phenyl-1,2,3-thiadiazolium bromide; References; 2 Structure of 1,2,3-Thiadiazoles; 2.1 Theoretical Methods; 2.2 Experimental Structural Methods; 2.2.1 X-ray Analysis; 2.2.2 Nuclear Magnetic Resonance Spectroscopy; 2.2.2.1 Proton NMR Spectroscopy; 2.2.2.2 Carbon-13 NMR Spectroscopy; 2.2.2.3 Nitrogen-14 NMR Spectroscopy; 2.2.2.4 Nitrogen-15 NMR Spectroscopy; 2.2.3 Mass Spectrometry; 2.2.4 Other Spectroscopic Data
References3 Chemical Properties of 1,2,3-Thiadiazoles; 3.1 Reactions due to the Reactivity of Ring Atoms; 3.1.1 Reactions with Electrophiles; 3.1.1.1 Protonation; 3.1.1.2 Complexation; 3.1.1.3 Alkylation; 3.1.1.4 Acylation; 3.1.1.5 Oxidation; 3.1.1.6 Electrophilic Substitution of Hydrogen; 3.1.2 Reactions with Nucleophiles; 3.1.2.1 Attack at the Sulfur Atom; 3.1.2.2 Attack at the C(5) Atom; 3.1.2.3 Attacks at H(4) and H(5); 3.1.2.4 Cycloaddition Reactions; 3.2 Reactions of Substituents; 3.2.1 5-Alkyl-1,2,3-thiadiazoles; 3.2.2 1,2,3-Thiadiazole-4-carbaldehyde
3.2.3 5-Amino-1,2,3-thiadiazole-4-carbothioamide
Record Nr. UNINA-9910143643403321
Bakulev Vasiliy A  
Hoboken, N.J., : John Wiley & Sons, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The chemistry of 1,2,3-Thiadiazoles [[electronic resource] /] / Vasiliy A. Bakulev, Wim Dehaen
The chemistry of 1,2,3-Thiadiazoles [[electronic resource] /] / Vasiliy A. Bakulev, Wim Dehaen
Autore Bakulev Vasiliy A
Pubbl/distr/stampa Hoboken, N.J., : John Wiley & Sons, c2004
Descrizione fisica 1 online resource (261 p.)
Disciplina 547.59
547.594
547/.59/05
Altri autori (Persone) DehaenW (Wim)
Collana The chemistry of heterocyclic compounds
Soggetto topico Thiadiazoles
ISBN 1-280-54200-4
9786610542000
0-471-65699-2
0-471-65691-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE CHEMISTRY OF 1,2,3-THIADIAZOLES; The Chemistry of Heterocyclic Compounds Introduction to the Series; Preface; Acknowledgments; Contents; 1 Synthesis of 1,2,3-thiadiazoles; 1.1 Cyclization of Hydrazones with Thionyl Chloride (Hurd-Mori Synthesis); 1.1.1 Scope and Limitations; 1.1.2 Mechanism of the Hurd-Mori Reaction; 1.1.3 Application of the Hurd-Mori Reaction in Organic Synthesis; 1.2 Cycloaddition of Diazoalkanes onto a C=S bond (Pechmann Synthesis); 1.3 Heterocyclization of α-diazo Thiocarbonyl Compounds (Wolff Synthesis)
1.3.1 Introduction of a Diazo Function into Compounds Containing a C=S Bond1.3.2 Introduction of a C=S Bond in the α-position to a Diazo Group; 1.3.3 Simultaneous Introduction of Diazo and Thiocarbonyl Functions; 1.4 Transformations of other Sulfur-containing Heterocyclic Compounds; 1.5 Elaboration of Preformed 1,2,3-Thiadiazoles; 1.5.1 Carboxylic Acids; 1.5.2 Functional Derivatives of Carboxylic Acids; 1.5.3 Aldehydes; 1.5.4 Amino-1,2,3-Thiadiazoles; 1.5.5 Halo Derivatives; 1.5.6 5-Hydrazino-, 5-Mercapto-1,2,3-Thiadiazoles and 5-Sulfide Derivatives
1.5.7 2-(1,2,3-Thiadiazol-5-yl)acetic Acid Derivatives1.5.8 Alkenyl-1,2,3-Thiadiazoles; 1.5.9 5-Hydroxyiminomethyl- and 5-Diazomethyl-1,2,3-Thiadiazoles; 1.5.10 4-Hydroxymethyl-1,2,3-Thiadiazoles; 1.6 Tables; 1.7 Selected Procedures; 1.7.1 1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.2 4-Phenyl-1,2,3-Thiadiazole; 1.7.3 4-Phenyl-1,2,3-Thiadiazole-5-Carbaldehyde; 1.7.4 4-Phenyl-5-Oxyiminomethyl-1,2,3-Thiadiazole; 1.7.5 5-Phenyl-1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.6 5-Chloro-1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.7 Ethyl 5-amino-1,2,3-Thiadiazole-4-Carboxylate; 1.7.7.1 Pechmann Method
1.7.7.2 Wolff Method1.7.8 Ethyl 5-chloro-1,2,3-Thiadiazole-4-Carboxylate; 1.7.9 4-Phenyl-2-(2,4,6-Trichlorophenyl)-1,2,3-Thiadiazolium Chloride; 1.7.10 5-Amino-4-ethoxycarbonyl-2-phenyl-1,2,3-thiadiazolium bromide; References; 2 Structure of 1,2,3-Thiadiazoles; 2.1 Theoretical Methods; 2.2 Experimental Structural Methods; 2.2.1 X-ray Analysis; 2.2.2 Nuclear Magnetic Resonance Spectroscopy; 2.2.2.1 Proton NMR Spectroscopy; 2.2.2.2 Carbon-13 NMR Spectroscopy; 2.2.2.3 Nitrogen-14 NMR Spectroscopy; 2.2.2.4 Nitrogen-15 NMR Spectroscopy; 2.2.3 Mass Spectrometry; 2.2.4 Other Spectroscopic Data
References3 Chemical Properties of 1,2,3-Thiadiazoles; 3.1 Reactions due to the Reactivity of Ring Atoms; 3.1.1 Reactions with Electrophiles; 3.1.1.1 Protonation; 3.1.1.2 Complexation; 3.1.1.3 Alkylation; 3.1.1.4 Acylation; 3.1.1.5 Oxidation; 3.1.1.6 Electrophilic Substitution of Hydrogen; 3.1.2 Reactions with Nucleophiles; 3.1.2.1 Attack at the Sulfur Atom; 3.1.2.2 Attack at the C(5) Atom; 3.1.2.3 Attacks at H(4) and H(5); 3.1.2.4 Cycloaddition Reactions; 3.2 Reactions of Substituents; 3.2.1 5-Alkyl-1,2,3-thiadiazoles; 3.2.2 1,2,3-Thiadiazole-4-carbaldehyde
3.2.3 5-Amino-1,2,3-thiadiazole-4-carbothioamide
Record Nr. UNINA-9910831037703321
Bakulev Vasiliy A  
Hoboken, N.J., : John Wiley & Sons, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The chemistry of 1,2,3-Thiadiazoles / / Vasiliy A. Bakulev, Wim Dehaen
The chemistry of 1,2,3-Thiadiazoles / / Vasiliy A. Bakulev, Wim Dehaen
Autore Bakulev Vasiliy A
Pubbl/distr/stampa Hoboken, N.J., : John Wiley & Sons, c2004
Descrizione fisica 1 online resource (261 p.)
Disciplina 547.59
547.594
547/.59/05
Altri autori (Persone) DehaenW (Wim)
Collana The chemistry of heterocyclic compounds
Soggetto topico Thiadiazoles
ISBN 9786610542000
9781280542008
1280542004
9780471656999
0471656992
9780471656913
0471656917
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE CHEMISTRY OF 1,2,3-THIADIAZOLES; The Chemistry of Heterocyclic Compounds Introduction to the Series; Preface; Acknowledgments; Contents; 1 Synthesis of 1,2,3-thiadiazoles; 1.1 Cyclization of Hydrazones with Thionyl Chloride (Hurd-Mori Synthesis); 1.1.1 Scope and Limitations; 1.1.2 Mechanism of the Hurd-Mori Reaction; 1.1.3 Application of the Hurd-Mori Reaction in Organic Synthesis; 1.2 Cycloaddition of Diazoalkanes onto a C=S bond (Pechmann Synthesis); 1.3 Heterocyclization of α-diazo Thiocarbonyl Compounds (Wolff Synthesis)
1.3.1 Introduction of a Diazo Function into Compounds Containing a C=S Bond1.3.2 Introduction of a C=S Bond in the α-position to a Diazo Group; 1.3.3 Simultaneous Introduction of Diazo and Thiocarbonyl Functions; 1.4 Transformations of other Sulfur-containing Heterocyclic Compounds; 1.5 Elaboration of Preformed 1,2,3-Thiadiazoles; 1.5.1 Carboxylic Acids; 1.5.2 Functional Derivatives of Carboxylic Acids; 1.5.3 Aldehydes; 1.5.4 Amino-1,2,3-Thiadiazoles; 1.5.5 Halo Derivatives; 1.5.6 5-Hydrazino-, 5-Mercapto-1,2,3-Thiadiazoles and 5-Sulfide Derivatives
1.5.7 2-(1,2,3-Thiadiazol-5-yl)acetic Acid Derivatives1.5.8 Alkenyl-1,2,3-Thiadiazoles; 1.5.9 5-Hydroxyiminomethyl- and 5-Diazomethyl-1,2,3-Thiadiazoles; 1.5.10 4-Hydroxymethyl-1,2,3-Thiadiazoles; 1.6 Tables; 1.7 Selected Procedures; 1.7.1 1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.2 4-Phenyl-1,2,3-Thiadiazole; 1.7.3 4-Phenyl-1,2,3-Thiadiazole-5-Carbaldehyde; 1.7.4 4-Phenyl-5-Oxyiminomethyl-1,2,3-Thiadiazole; 1.7.5 5-Phenyl-1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.6 5-Chloro-1,2,3-Thiadiazole-4-Carbaldehyde; 1.7.7 Ethyl 5-amino-1,2,3-Thiadiazole-4-Carboxylate; 1.7.7.1 Pechmann Method
1.7.7.2 Wolff Method1.7.8 Ethyl 5-chloro-1,2,3-Thiadiazole-4-Carboxylate; 1.7.9 4-Phenyl-2-(2,4,6-Trichlorophenyl)-1,2,3-Thiadiazolium Chloride; 1.7.10 5-Amino-4-ethoxycarbonyl-2-phenyl-1,2,3-thiadiazolium bromide; References; 2 Structure of 1,2,3-Thiadiazoles; 2.1 Theoretical Methods; 2.2 Experimental Structural Methods; 2.2.1 X-ray Analysis; 2.2.2 Nuclear Magnetic Resonance Spectroscopy; 2.2.2.1 Proton NMR Spectroscopy; 2.2.2.2 Carbon-13 NMR Spectroscopy; 2.2.2.3 Nitrogen-14 NMR Spectroscopy; 2.2.2.4 Nitrogen-15 NMR Spectroscopy; 2.2.3 Mass Spectrometry; 2.2.4 Other Spectroscopic Data
References3 Chemical Properties of 1,2,3-Thiadiazoles; 3.1 Reactions due to the Reactivity of Ring Atoms; 3.1.1 Reactions with Electrophiles; 3.1.1.1 Protonation; 3.1.1.2 Complexation; 3.1.1.3 Alkylation; 3.1.1.4 Acylation; 3.1.1.5 Oxidation; 3.1.1.6 Electrophilic Substitution of Hydrogen; 3.1.2 Reactions with Nucleophiles; 3.1.2.1 Attack at the Sulfur Atom; 3.1.2.2 Attack at the C(5) Atom; 3.1.2.3 Attacks at H(4) and H(5); 3.1.2.4 Cycloaddition Reactions; 3.2 Reactions of Substituents; 3.2.1 5-Alkyl-1,2,3-thiadiazoles; 3.2.2 1,2,3-Thiadiazole-4-carbaldehyde
3.2.3 5-Amino-1,2,3-thiadiazole-4-carbothioamide
Record Nr. UNINA-9911020229203321
Bakulev Vasiliy A  
Hoboken, N.J., : John Wiley & Sons, c2004
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Compounds with condensed thiophene rings [[electronic resource] /] / H.D. Hartough and S.L. Meisel
Compounds with condensed thiophene rings [[electronic resource] /] / H.D. Hartough and S.L. Meisel
Autore Hartough H. D (Howard Dale), <1913-1992.>
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience, 1954
Descrizione fisica 1 online resource (534 p.)
Disciplina 547.594
547/.59/05
Altri autori (Persone) MeiselS. L <1922-> (Seymour Lionel)
Collana Chemistry of heterocyclic compounds
Soggetto topico Thiophenes
Chemistry
ISBN 1-282-30141-1
9786612301414
0-470-18656-9
0-470-18806-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto COMPOUNDS WITH CONDENSED THIOPHENE RINGS; CONTENTS; I. Factors Influencing Chemical Reactivity and Substitution of Thiophene Systems; I. Introduction; II. Electrophilic Substitution of Furan, Thiophene and Selenophene; III. Electrophilic Substitution of Benzofuran, Thianaphthene, Selenonaphthene and the Thienothiophenes; IV. Electrophilic Substitution of Dibenzofuran, Dibenzothiophene and Dibenzoselenophene; V. Metalation of Thiophene Systems; VI. Reactivity of the Sulfur Atom in Thiophene Systems; II. Thianaphthene and Other Thiophene Compounds Containing One Carbocyclic Fused Ring
IntroductionA. Thianaphthene and Its Derivatives; Nomenclature; Occurrence of Thianaphthene Nature; I. Preparation of Thianaphthene and Its Homologs; A. Thianaphthene; B. Monoalkylthianaphthenes; C. Dialkylthianaphthenes; D. Trialkylthianaphthenes; E. Arylthianaphthenes; II. Miscellaneous Reactions and Properties; III. The Hydrothianaphthenes; A. 2,3-Dihydrothianaphthene and Its Derivatives; B. 6,7-Dihydrothianaphthene; C. 4,5,6,7-Tetrahydrothianaphthene and Its Derivatives; IV. Halogen Derivatives; V. Nitrogen Derivatives; A. Nitrothianaphthenes; B. Aminothianaphthenes
C. Derivatives with Nitrogen in a Side ChainVI. Hydroxythianaphthenes (Thianaphthenols or Thioindoxyls); A. Tautomerism of 2- and 3-Hydroxythisanaphthenes; B. Preparation of Hydroxythianaphthenes; 1. 2-Hydroxythianaphthenes; 2. 3-Hydroxythianaphthenes; 3. 4-Hydroxythianaphthenes; 4. 5-Hydroxythianaphthenes; 5. 6-Hydroxythianaphthenes; 6. 7-Hgdroxythianaphthenes; 7. Di- and Trihydroxythianaphthenes; C. Reactions of Hydroxythianaphthenes; 1. Reactions of the Enol Form; 2. Reactions of the Keto From; VII. Thianaphthenequinones; A. 2,3-Thinaphthenequinones; B. Benzenoid Thianaphthenequinones
1. 4,5-Thianaphthmequinones2. 6,7-Thianaphthenequinones; 3. 4,7-Thianaphthenequinones; VIII. Derivatives Containing Hydroxyl Groups in a Side Chain; IX. Carbonyl Derivatives; A. Thianaphthenecarboxaldehydes; B. Keto Derivatives of Thianaphthene; X. Thianaphthenecarboxylic Acids; A. Monocarboxylic Acids; B. 2,3-Thianaphthenedicarboxylic Acid and Its Derivatives; C. 3-Amino-2-thianaphthenecarboxylic Acid; D. 3-Hydroxy-2-thianaphthencarboxylic Acid; E. Thianaphthenecarboxylic Acids with the Carboxyl Group in the Side Chain; XI. Thianaphthenesulfonic Acids and Thianaphthene Sulfides
XII. Mercury DerivativesXIII. Thianaphthene l-Oxides (Sulfoxides); XIV. Thianaphthene 1-Dioxides (Sulfones); A. Preparation; B. Reactions; B. Isothianaphthene and Its Derivatives; I. The Hydroisothianaphthenes; A. 1.3-Dihydroisothianaphthene o-Xylylene Sulfide); B. 6,7-Dihydro- and 4,5,6,7-Tetrahydroistothianaphthenes; II. Derivatives of Isothianaphthene; C. Miscellaneous Systems; I. Cyclopenta [b]thiophene; II. Cyclohepta[b]thiophene; III. 4,7-Endovinylenethianaphthene; III. Thioindigo and Related Dyes; Introduction; I. Nomenclature; II. Friedländer's Commercial Thioindigo Synthesis
III. Symmetrical Thioindigo Dyes
Record Nr. UNINA-9910144289003321
Hartough H. D (Howard Dale), <1913-1992.>  
New York, : Interscience, 1954
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Compounds with condensed thiophene rings [[electronic resource] /] / H.D. Hartough and S.L. Meisel
Compounds with condensed thiophene rings [[electronic resource] /] / H.D. Hartough and S.L. Meisel
Autore Hartough H. D (Howard Dale), <1913-1992.>
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience, 1954
Descrizione fisica 1 online resource (534 p.)
Disciplina 547.594
547/.59/05
Altri autori (Persone) MeiselS. L <1922-> (Seymour Lionel)
Collana Chemistry of heterocyclic compounds
Soggetto topico Thiophenes
Chemistry
ISBN 1-282-30141-1
9786612301414
0-470-18656-9
0-470-18806-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto COMPOUNDS WITH CONDENSED THIOPHENE RINGS; CONTENTS; I. Factors Influencing Chemical Reactivity and Substitution of Thiophene Systems; I. Introduction; II. Electrophilic Substitution of Furan, Thiophene and Selenophene; III. Electrophilic Substitution of Benzofuran, Thianaphthene, Selenonaphthene and the Thienothiophenes; IV. Electrophilic Substitution of Dibenzofuran, Dibenzothiophene and Dibenzoselenophene; V. Metalation of Thiophene Systems; VI. Reactivity of the Sulfur Atom in Thiophene Systems; II. Thianaphthene and Other Thiophene Compounds Containing One Carbocyclic Fused Ring
IntroductionA. Thianaphthene and Its Derivatives; Nomenclature; Occurrence of Thianaphthene Nature; I. Preparation of Thianaphthene and Its Homologs; A. Thianaphthene; B. Monoalkylthianaphthenes; C. Dialkylthianaphthenes; D. Trialkylthianaphthenes; E. Arylthianaphthenes; II. Miscellaneous Reactions and Properties; III. The Hydrothianaphthenes; A. 2,3-Dihydrothianaphthene and Its Derivatives; B. 6,7-Dihydrothianaphthene; C. 4,5,6,7-Tetrahydrothianaphthene and Its Derivatives; IV. Halogen Derivatives; V. Nitrogen Derivatives; A. Nitrothianaphthenes; B. Aminothianaphthenes
C. Derivatives with Nitrogen in a Side ChainVI. Hydroxythianaphthenes (Thianaphthenols or Thioindoxyls); A. Tautomerism of 2- and 3-Hydroxythisanaphthenes; B. Preparation of Hydroxythianaphthenes; 1. 2-Hydroxythianaphthenes; 2. 3-Hydroxythianaphthenes; 3. 4-Hydroxythianaphthenes; 4. 5-Hydroxythianaphthenes; 5. 6-Hydroxythianaphthenes; 6. 7-Hgdroxythianaphthenes; 7. Di- and Trihydroxythianaphthenes; C. Reactions of Hydroxythianaphthenes; 1. Reactions of the Enol Form; 2. Reactions of the Keto From; VII. Thianaphthenequinones; A. 2,3-Thinaphthenequinones; B. Benzenoid Thianaphthenequinones
1. 4,5-Thianaphthmequinones2. 6,7-Thianaphthenequinones; 3. 4,7-Thianaphthenequinones; VIII. Derivatives Containing Hydroxyl Groups in a Side Chain; IX. Carbonyl Derivatives; A. Thianaphthenecarboxaldehydes; B. Keto Derivatives of Thianaphthene; X. Thianaphthenecarboxylic Acids; A. Monocarboxylic Acids; B. 2,3-Thianaphthenedicarboxylic Acid and Its Derivatives; C. 3-Amino-2-thianaphthenecarboxylic Acid; D. 3-Hydroxy-2-thianaphthencarboxylic Acid; E. Thianaphthenecarboxylic Acids with the Carboxyl Group in the Side Chain; XI. Thianaphthenesulfonic Acids and Thianaphthene Sulfides
XII. Mercury DerivativesXIII. Thianaphthene l-Oxides (Sulfoxides); XIV. Thianaphthene 1-Dioxides (Sulfones); A. Preparation; B. Reactions; B. Isothianaphthene and Its Derivatives; I. The Hydroisothianaphthenes; A. 1.3-Dihydroisothianaphthene o-Xylylene Sulfide); B. 6,7-Dihydro- and 4,5,6,7-Tetrahydroistothianaphthenes; II. Derivatives of Isothianaphthene; C. Miscellaneous Systems; I. Cyclopenta [b]thiophene; II. Cyclohepta[b]thiophene; III. 4,7-Endovinylenethianaphthene; III. Thioindigo and Related Dyes; Introduction; I. Nomenclature; II. Friedländer's Commercial Thioindigo Synthesis
III. Symmetrical Thioindigo Dyes
Record Nr. UNISA-996202936203316
Hartough H. D (Howard Dale), <1913-1992.>  
New York, : Interscience, 1954
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Compounds with condensed thiophene rings [[electronic resource] /] / H.D. Hartough and S.L. Meisel
Compounds with condensed thiophene rings [[electronic resource] /] / H.D. Hartough and S.L. Meisel
Autore Hartough H. D (Howard Dale), <1913-1992.>
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience, 1954
Descrizione fisica 1 online resource (534 p.)
Disciplina 547.594
547/.59/05
Altri autori (Persone) MeiselS. L <1922-> (Seymour Lionel)
Collana Chemistry of heterocyclic compounds
Soggetto topico Thiophenes
Chemistry
ISBN 1-282-30141-1
9786612301414
0-470-18656-9
0-470-18806-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto COMPOUNDS WITH CONDENSED THIOPHENE RINGS; CONTENTS; I. Factors Influencing Chemical Reactivity and Substitution of Thiophene Systems; I. Introduction; II. Electrophilic Substitution of Furan, Thiophene and Selenophene; III. Electrophilic Substitution of Benzofuran, Thianaphthene, Selenonaphthene and the Thienothiophenes; IV. Electrophilic Substitution of Dibenzofuran, Dibenzothiophene and Dibenzoselenophene; V. Metalation of Thiophene Systems; VI. Reactivity of the Sulfur Atom in Thiophene Systems; II. Thianaphthene and Other Thiophene Compounds Containing One Carbocyclic Fused Ring
IntroductionA. Thianaphthene and Its Derivatives; Nomenclature; Occurrence of Thianaphthene Nature; I. Preparation of Thianaphthene and Its Homologs; A. Thianaphthene; B. Monoalkylthianaphthenes; C. Dialkylthianaphthenes; D. Trialkylthianaphthenes; E. Arylthianaphthenes; II. Miscellaneous Reactions and Properties; III. The Hydrothianaphthenes; A. 2,3-Dihydrothianaphthene and Its Derivatives; B. 6,7-Dihydrothianaphthene; C. 4,5,6,7-Tetrahydrothianaphthene and Its Derivatives; IV. Halogen Derivatives; V. Nitrogen Derivatives; A. Nitrothianaphthenes; B. Aminothianaphthenes
C. Derivatives with Nitrogen in a Side ChainVI. Hydroxythianaphthenes (Thianaphthenols or Thioindoxyls); A. Tautomerism of 2- and 3-Hydroxythisanaphthenes; B. Preparation of Hydroxythianaphthenes; 1. 2-Hydroxythianaphthenes; 2. 3-Hydroxythianaphthenes; 3. 4-Hydroxythianaphthenes; 4. 5-Hydroxythianaphthenes; 5. 6-Hydroxythianaphthenes; 6. 7-Hgdroxythianaphthenes; 7. Di- and Trihydroxythianaphthenes; C. Reactions of Hydroxythianaphthenes; 1. Reactions of the Enol Form; 2. Reactions of the Keto From; VII. Thianaphthenequinones; A. 2,3-Thinaphthenequinones; B. Benzenoid Thianaphthenequinones
1. 4,5-Thianaphthmequinones2. 6,7-Thianaphthenequinones; 3. 4,7-Thianaphthenequinones; VIII. Derivatives Containing Hydroxyl Groups in a Side Chain; IX. Carbonyl Derivatives; A. Thianaphthenecarboxaldehydes; B. Keto Derivatives of Thianaphthene; X. Thianaphthenecarboxylic Acids; A. Monocarboxylic Acids; B. 2,3-Thianaphthenedicarboxylic Acid and Its Derivatives; C. 3-Amino-2-thianaphthenecarboxylic Acid; D. 3-Hydroxy-2-thianaphthencarboxylic Acid; E. Thianaphthenecarboxylic Acids with the Carboxyl Group in the Side Chain; XI. Thianaphthenesulfonic Acids and Thianaphthene Sulfides
XII. Mercury DerivativesXIII. Thianaphthene l-Oxides (Sulfoxides); XIV. Thianaphthene 1-Dioxides (Sulfones); A. Preparation; B. Reactions; B. Isothianaphthene and Its Derivatives; I. The Hydroisothianaphthenes; A. 1.3-Dihydroisothianaphthene o-Xylylene Sulfide); B. 6,7-Dihydro- and 4,5,6,7-Tetrahydroistothianaphthenes; II. Derivatives of Isothianaphthene; C. Miscellaneous Systems; I. Cyclopenta [b]thiophene; II. Cyclohepta[b]thiophene; III. 4,7-Endovinylenethianaphthene; III. Thioindigo and Related Dyes; Introduction; I. Nomenclature; II. Friedländer's Commercial Thioindigo Synthesis
III. Symmetrical Thioindigo Dyes
Record Nr. UNINA-9910830072603321
Hartough H. D (Howard Dale), <1913-1992.>  
New York, : Interscience, 1954
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Compounds with condensed thiophene rings / / H.D. Hartough and S.L. Meisel
Compounds with condensed thiophene rings / / H.D. Hartough and S.L. Meisel
Autore Hartough H. D (Howard Dale), <1913-1992.>
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience, 1954
Descrizione fisica 1 online resource (534 p.)
Disciplina 547.594
547/.59/05
Altri autori (Persone) MeiselS. L <1922-> (Seymour Lionel)
Collana Chemistry of heterocyclic compounds
Soggetto topico Thiophenes
Chemistry
ISBN 9786612301414
9781282301412
1282301411
9780470186565
0470186569
9780470188064
0470188065
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto COMPOUNDS WITH CONDENSED THIOPHENE RINGS; CONTENTS; I. Factors Influencing Chemical Reactivity and Substitution of Thiophene Systems; I. Introduction; II. Electrophilic Substitution of Furan, Thiophene and Selenophene; III. Electrophilic Substitution of Benzofuran, Thianaphthene, Selenonaphthene and the Thienothiophenes; IV. Electrophilic Substitution of Dibenzofuran, Dibenzothiophene and Dibenzoselenophene; V. Metalation of Thiophene Systems; VI. Reactivity of the Sulfur Atom in Thiophene Systems; II. Thianaphthene and Other Thiophene Compounds Containing One Carbocyclic Fused Ring
IntroductionA. Thianaphthene and Its Derivatives; Nomenclature; Occurrence of Thianaphthene Nature; I. Preparation of Thianaphthene and Its Homologs; A. Thianaphthene; B. Monoalkylthianaphthenes; C. Dialkylthianaphthenes; D. Trialkylthianaphthenes; E. Arylthianaphthenes; II. Miscellaneous Reactions and Properties; III. The Hydrothianaphthenes; A. 2,3-Dihydrothianaphthene and Its Derivatives; B. 6,7-Dihydrothianaphthene; C. 4,5,6,7-Tetrahydrothianaphthene and Its Derivatives; IV. Halogen Derivatives; V. Nitrogen Derivatives; A. Nitrothianaphthenes; B. Aminothianaphthenes
C. Derivatives with Nitrogen in a Side ChainVI. Hydroxythianaphthenes (Thianaphthenols or Thioindoxyls); A. Tautomerism of 2- and 3-Hydroxythisanaphthenes; B. Preparation of Hydroxythianaphthenes; 1. 2-Hydroxythianaphthenes; 2. 3-Hydroxythianaphthenes; 3. 4-Hydroxythianaphthenes; 4. 5-Hydroxythianaphthenes; 5. 6-Hydroxythianaphthenes; 6. 7-Hgdroxythianaphthenes; 7. Di- and Trihydroxythianaphthenes; C. Reactions of Hydroxythianaphthenes; 1. Reactions of the Enol Form; 2. Reactions of the Keto From; VII. Thianaphthenequinones; A. 2,3-Thinaphthenequinones; B. Benzenoid Thianaphthenequinones
1. 4,5-Thianaphthmequinones2. 6,7-Thianaphthenequinones; 3. 4,7-Thianaphthenequinones; VIII. Derivatives Containing Hydroxyl Groups in a Side Chain; IX. Carbonyl Derivatives; A. Thianaphthenecarboxaldehydes; B. Keto Derivatives of Thianaphthene; X. Thianaphthenecarboxylic Acids; A. Monocarboxylic Acids; B. 2,3-Thianaphthenedicarboxylic Acid and Its Derivatives; C. 3-Amino-2-thianaphthenecarboxylic Acid; D. 3-Hydroxy-2-thianaphthencarboxylic Acid; E. Thianaphthenecarboxylic Acids with the Carboxyl Group in the Side Chain; XI. Thianaphthenesulfonic Acids and Thianaphthene Sulfides
XII. Mercury DerivativesXIII. Thianaphthene l-Oxides (Sulfoxides); XIV. Thianaphthene 1-Dioxides (Sulfones); A. Preparation; B. Reactions; B. Isothianaphthene and Its Derivatives; I. The Hydroisothianaphthenes; A. 1.3-Dihydroisothianaphthene o-Xylylene Sulfide); B. 6,7-Dihydro- and 4,5,6,7-Tetrahydroistothianaphthenes; II. Derivatives of Isothianaphthene; C. Miscellaneous Systems; I. Cyclopenta [b]thiophene; II. Cyclohepta[b]thiophene; III. 4,7-Endovinylenethianaphthene; III. Thioindigo and Related Dyes; Introduction; I. Nomenclature; II. Friedländer's Commercial Thioindigo Synthesis
III. Symmetrical Thioindigo Dyes
Record Nr. UNINA-9911019086503321
Hartough H. D (Howard Dale), <1913-1992.>  
New York, : Interscience, 1954
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Handbook of oligo- and polythiophenes / / Denis Fichou
Handbook of oligo- and polythiophenes / / Denis Fichou
Autore Fichou Denis
Pubbl/distr/stampa Weinheim, [Germany] : , : Wiley-VCH, , 1999
Descrizione fisica 1 online resource (560 p.)
Disciplina 547.594
547.7
Altri autori (Persone) FichouDenis
Soggetto topico Thiophenes
Polythiophenes
Soggetto genere / forma Electronic books.
ISBN 1-282-01020-4
9786612010200
3-527-61171-1
3-527-61170-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Handbook of Oligo- and Polythiophenes; Contents; 1 The Chemistry of Conducting Polythiophenes: from Synthesis to Self-Assembly to Intelligent Materials; 1.1 Introduction; 1.2 Chemical Synthesis of Unsubstituted Polythiophene (PT); 1.3 Chemcial Synthesis of Polyalkylthiophenes (PATs); 1.3.1 Straight Alkyl Side Chains; 1.3.1.1 Chemical Synthesis of PATs; 1.3.1.1.1 Metal Catalyed Cross-coupling Polymerizations; 1.3.1.1.2 FeCl3 Method for the Polymerization of PATs; 1.3.1.2 Comparison of the Above Methods; 1.3.1.3 Regioregular PATs; 1.3.1.3.1 Regioregular HH-TT and TT-HH PATs
1.3.1.4 Regioregular, Head-to-Tail Coupled PATs1.3.1.4.1 The McCullough Method; 1.3.1.4.2 The Rieke Method; 1.3.1.4.3 The Mechanism and Catalyst Choice; 1.3.1.4.4 NMR Characterization of HT-PAT; 1.3.1.4.5 IR and UV-Vis; 1.3.1.4.6 Self-Assembly, X-ray, and Electrical Conductivity in HT-PATs; 1.3.1.4.7 Other Methods; 1.3.1.4.8 Random Copolymers of Alkyl Thiophenes; 1.3.1.4.9 Head-to-Tail Coupled, Random Copolymers of Alkyl Thiophenes; 1.3.1.5 Branched Alkyl PATs; 1.3.1.6 PTs with Phenyl Sidechains
1.4 Chemical Synthesis of Heteroatomic Functionalized Substituents on PTs: Recognition Sites for Self-Assembly and Chemical Sensing1.4.1 Chemical Synthesis of Alkoxy Polythiophenes; 1.4.2 Chemical Prepared Alkoxy PTs as Conducting Polymer Sensors; 1.4.3 Chiral Substituents on PT; 1.4.4 Carboxylic Acid Derivatives: Self-Assembly and Sensors; 1.4.5 Other Derivatives of PT; 1.5 Fused Rings Systems; 1.6 Conclusion; References; 2 Electronic Properties of Polythiophenes; 2.1 General Aspects of Conducting Polymers; 2.2 Structure and Conformation of Polythiophenes
2.2.1 Morphology and Crystal Structure2.2.2 Conformational Features; 2.3 Electronic Processes of Polythiophenes; 2.3.1 Charge Excitations in Polythiophenes; 2.3.2 Charge Transport in Polythiophenes; 2.3.3 Carrier Recombination: Photoluminescence and Electroluminescence; 2.3.4 Spectroscopic Studies of the Charged States; 2.3.4.1 Charge Storage Configurations in Solids and their Anisotropic Properties; 2.3.4.2 Properties in Solutions; 2.4 Concluding Remarks and Future Outlook; Acknowledgments; References; 3 The Synthesis of Oligothiphenes; 3.1 Introduction; 3.2 Synthesis of Oligothiophenes
3.2.1 Unsubstituted Oligothiphenes3.2.1.1 Arene/arene-Coupling Methods by Oxidative Couplings; 3.2.1.2 Transition Metal Catalyzed Coupling Methods; 3.2.1.3 Ring Closure Reactions from Acyclic Precursors; 3.2.1.4 Physical Properties of α-Oligothiophenes and Isomers; 3.2.2 Substituted Oligothiophenes; 3.2.2.1 ß,ß-Substituted Oligothiophenes; 3.2.2.2 α,α'-Substituted Oligothiophenes; 3.2.2.3 α,β-Substituted Oligothiophenes; 3.2.2.4 Functionalized Oligothiophenes; 3.2.2.5 Amphiphilic Oligothiophenes; 3.2.2.6 Transition Metal Complexes of Oligothiophenes; 3.3 Conclusion; Acknowledgement
References
Record Nr. UNINA-9910144723803321
Fichou Denis  
Weinheim, [Germany] : , : Wiley-VCH, , 1999
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Handbook of oligo- and polythiophenes / / Denis Fichou
Handbook of oligo- and polythiophenes / / Denis Fichou
Autore Fichou Denis
Pubbl/distr/stampa Weinheim, [Germany] : , : Wiley-VCH, , 1999
Descrizione fisica 1 online resource (560 p.)
Disciplina 547.594
547.7
Altri autori (Persone) FichouDenis
Soggetto topico Thiophenes
Polythiophenes
ISBN 1-282-01020-4
9786612010200
3-527-61171-1
3-527-61170-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Handbook of Oligo- and Polythiophenes; Contents; 1 The Chemistry of Conducting Polythiophenes: from Synthesis to Self-Assembly to Intelligent Materials; 1.1 Introduction; 1.2 Chemical Synthesis of Unsubstituted Polythiophene (PT); 1.3 Chemcial Synthesis of Polyalkylthiophenes (PATs); 1.3.1 Straight Alkyl Side Chains; 1.3.1.1 Chemical Synthesis of PATs; 1.3.1.1.1 Metal Catalyed Cross-coupling Polymerizations; 1.3.1.1.2 FeCl3 Method for the Polymerization of PATs; 1.3.1.2 Comparison of the Above Methods; 1.3.1.3 Regioregular PATs; 1.3.1.3.1 Regioregular HH-TT and TT-HH PATs
1.3.1.4 Regioregular, Head-to-Tail Coupled PATs1.3.1.4.1 The McCullough Method; 1.3.1.4.2 The Rieke Method; 1.3.1.4.3 The Mechanism and Catalyst Choice; 1.3.1.4.4 NMR Characterization of HT-PAT; 1.3.1.4.5 IR and UV-Vis; 1.3.1.4.6 Self-Assembly, X-ray, and Electrical Conductivity in HT-PATs; 1.3.1.4.7 Other Methods; 1.3.1.4.8 Random Copolymers of Alkyl Thiophenes; 1.3.1.4.9 Head-to-Tail Coupled, Random Copolymers of Alkyl Thiophenes; 1.3.1.5 Branched Alkyl PATs; 1.3.1.6 PTs with Phenyl Sidechains
1.4 Chemical Synthesis of Heteroatomic Functionalized Substituents on PTs: Recognition Sites for Self-Assembly and Chemical Sensing1.4.1 Chemical Synthesis of Alkoxy Polythiophenes; 1.4.2 Chemical Prepared Alkoxy PTs as Conducting Polymer Sensors; 1.4.3 Chiral Substituents on PT; 1.4.4 Carboxylic Acid Derivatives: Self-Assembly and Sensors; 1.4.5 Other Derivatives of PT; 1.5 Fused Rings Systems; 1.6 Conclusion; References; 2 Electronic Properties of Polythiophenes; 2.1 General Aspects of Conducting Polymers; 2.2 Structure and Conformation of Polythiophenes
2.2.1 Morphology and Crystal Structure2.2.2 Conformational Features; 2.3 Electronic Processes of Polythiophenes; 2.3.1 Charge Excitations in Polythiophenes; 2.3.2 Charge Transport in Polythiophenes; 2.3.3 Carrier Recombination: Photoluminescence and Electroluminescence; 2.3.4 Spectroscopic Studies of the Charged States; 2.3.4.1 Charge Storage Configurations in Solids and their Anisotropic Properties; 2.3.4.2 Properties in Solutions; 2.4 Concluding Remarks and Future Outlook; Acknowledgments; References; 3 The Synthesis of Oligothiphenes; 3.1 Introduction; 3.2 Synthesis of Oligothiophenes
3.2.1 Unsubstituted Oligothiphenes3.2.1.1 Arene/arene-Coupling Methods by Oxidative Couplings; 3.2.1.2 Transition Metal Catalyzed Coupling Methods; 3.2.1.3 Ring Closure Reactions from Acyclic Precursors; 3.2.1.4 Physical Properties of α-Oligothiophenes and Isomers; 3.2.2 Substituted Oligothiophenes; 3.2.2.1 ß,ß-Substituted Oligothiophenes; 3.2.2.2 α,α'-Substituted Oligothiophenes; 3.2.2.3 α,β-Substituted Oligothiophenes; 3.2.2.4 Functionalized Oligothiophenes; 3.2.2.5 Amphiphilic Oligothiophenes; 3.2.2.6 Transition Metal Complexes of Oligothiophenes; 3.3 Conclusion; Acknowledgement
References
Record Nr. UNINA-9910831100203321
Fichou Denis  
Weinheim, [Germany] : , : Wiley-VCH, , 1999
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Multi-sulfur and sulfur and oxygen five- and six-membered heterocycles . Part one [[electronic resource] /] / David S. Breslow, Herman Skolnik
Multi-sulfur and sulfur and oxygen five- and six-membered heterocycles . Part one [[electronic resource] /] / David S. Breslow, Herman Skolnik
Autore Breslow David Samuel <1916->
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience, 1966
Descrizione fisica 1 online resource (635 p.)
Disciplina 547.594
547/.59/05
Altri autori (Persone) SkolnikHerman
Collana Chemistry of heterocyclic compounds
Soggetto topico Organosulfur compounds
Heterocyclic compounds
ISBN 1-282-30160-8
9786612301605
0-470-18682-8
0-470-18832-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto MULTI-SULFUR AND SULFUR AND OXYGEN FIVE- AND SIXMEMBERED HETEROCYCLES; CONTENTS OF PART ONE; 1. C2O2S Ring Systems; I. C2O2S 1, 3, 2-Dioxathiolane and 1, 3, 2-Dioxathiole; A. Sulfite Esters of 1, 2-Glycols; 1. Preparation; 2. Structure and Physical Properties; 3. Reactions; 4. Uses; B. Sulfate Esters of 1, 2-Glycols; 1. Preparation; 2. Structure and Reactions; C. Sulfate Esters of Enediols; D. 1, 3, 2-Dioxathiolan-4-one 2-Oxides; II. C4-C2O2S 2, 4-Dioxa-3-thiabicyclo[3. 2. 0]heptane; III. C2O2S-C2O2S 1, 3, 2-Dioxathiolo[1, 3, 2]dioxathiole Glyoxal Sulfate
IV. C2O2S-C4O Furo[3, 4-d]-l, 3, 2-dioxathioleV. C2O2S-C4S Thieno[3, 4-d]-1, 3, 2-dioxathiole; VI. C2O2S-C5 3aH-Cyclopenta-1, 3, 2-dioxathiole; VII. C2O2S-C5O 4H-Pyrano[3, 4-d]-1, 3, 2-dioxathiole; VIII. C2O2S-C6 1, 3, 2-Benzodioxathiole; A. Sulfite Esters; B. Sulfate Esters; IX. C2O2S-C7 4H-Cyclohepta-1, 3, 2-dioxathiole; X. C2O2S-C4O-C4O 1, 7, 11, 13-Tetraoxa-12-thiadispiro-[4. 0. 4. 3]trideca-3, 9-diene-2, 8-dione; XI. C2O2S-C4N-C5N 6H-Cyclohepta-1, 3, 2-dioxathiol-4, 8-imine; XII. C2O2S-C5-C6 8H-Indeno[1, 2-d}-1, 3, 2-dioxathiole
XIII. C2O2S-C4O2-C50 4H, 6H-1, 3, 2-Dioxathiolo[4, 5]-pyrano[3, 2-d]-m-dioxinXIV. C2O2S-C6C6; A. Naphtho[1, 2-d}-1, 3, 2-dioxathiole; B. Naphtho[2, 3-d]-1, 3, 2-dioxathiole; XV. C2O2S-C6-C6-C6; A. Anthra[1, 2-d]-1, 3, 2-dioxathiole; 1. Sulfite Esters; 2. Sulfate Esters; B. Anthra[2, 3-d]-1, 3, 2-dioxathiole; C. Phenanthro[9, 10-d]-1, 3, 2-dioxathiole; XVI. C2O2S-C4N-C4N-C9O2 [1, 3, 2]Dioxathiolo-[4', 5' : 8, 9][1, 6]dioxacycloundeca[2, 3, 4-gh]-pyrrolizine; XVII. C2O2S-C4N-C4N-C10O2 Spiro[1, 6]dioxacyclododeca-[2, 3, 4-gh]-pyrrolizine-9(8H), 4'-[ 1, 3, 2]-dioxathiolane
XVIII. C2O2S-C5-C6-C6-C6A. Cyclopenta[1, 2]phenanthro[4, 4a-d][1, 3, 2]-dioxathiole; B. Cyclopenta[1, 2]phenanthro[1, 10a-d][1, 3, 2]-dioxathiole; XIX. C2O2S-C6-C6-C6-C6; A. Chryseno[5, 6-d]-1, 3, 2-dioxathiole; B. 4, 9-o-Benzenonaphtho[2, 3-d]-1, 3, 2-dioxathiole; XX. C2O2S-C4O-C4O-C5-C6-C6 3H, 9H-11b, 13a-Epoxycyclopenta[1, 2]phenanthro[4, 4a-d][1, 3, 2]dioxathiole; 2. C2OS2 Ring Systems; I. 1, 2, 5-Oxadithia Compounds; A. C2OS2 1, 2, 5-Oxadithiolane; B. C2OS2-C4SThieno[3, 4-c][1, 2, 5]oxadithiole; C. C2OS2-C6 2, 1, 3-Benzoxadithiole; D. C2OS2-C6-C6 Naphth[1, 2-c][1, 2, 5]oxadithiole
II. 1, 3, 4-Oxadithia CompoundsC2OS2 1, 3, 4-Oxadithiolane; 3. C2S3 Ring Systems; I. 1, 2, 3-Trithia Compounds; A. C2S3 1,2,3-Trithiole; B. C2S3-C6 Benzotrithiole; C. C2S3-C4N2-C6 Trithiolo[4, 5-b]quinoxaline; II. 1, 2, 4-Trithia Compounds; A. C2S3 1, 2, 4-Trithiolane; B. Spiro Derivatives of 1, 2, 4-Trithiolane; 4. C3OS Ring Systems; I. 1, 2-Oxathia Compounds; A. C3OS 5H-1, 2-Oxathiole, 3H-1, 2-Oxathiole, and 1, 2-Oxathiolane; 1. 3H-1, 2-Oxathiole; 2. 5H-1, 2-Oxathiole; 3. 1, 2-Oxathiolane; a. 1, 2-Oxathiolane 2, 2-Dioxide; (1) Preparation; (a) From 3-Chloroalkanesulfonic Acids
(b) From 3-Hydroxyalkanesulphonic Acids
Record Nr. UNINA-9910144284003321
Breslow David Samuel <1916->  
New York, : Interscience, 1966
Materiale a stampa
Lo trovi qui: Univ. Federico II
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