01018nam0 22003011i 450 RML026703220231121125723.020121121d1982 ||||0itac50 baitaitz01i xxxe z01nLorenzo Vianidi Rita Baldassarri[Firenze] La Nuova Italia 1982116 p.17 cm˜Il œcastoro 189001RML03305372001 ˜Il œcastoro 189Viani, LorenzoFIRRMLC231303I853.912NARRATIVA ITALIANA, 1900-194521Baldassarri, RitaRMLV171972152182ITIT-0120121121IT-FR0017 Biblioteca umanistica Giorgio ApreaFR0017 RML0267032Biblioteca umanistica Giorgio Aprea 52MAG 1 COLL E 189 52DUP0009015085 VMB RS A 2018112620181126 52Lorenzo Viani102937UNICAS05359nam 2200733Ia 450 991102014030332120200520144314.09786612301711978128230171912823017139780470186961047018696897804701884530470188456(CKB)1000000000376552(EBL)469845(OCoLC)814417555(SSID)ssj0000365763(PQKBManifestationID)11229993(PQKBTitleCode)TC0000365763(PQKBWorkID)10423072(PQKB)10681182(MiAaPQ)EBC469845(PPN)248095714(Perlego)2775112(EXLCZ)99100000000037655220720131d1972 uy 0engur|n|---|||||txtccrSeven-membered heterocyclic compounds containing oxygen and sulfur /edited by Andre Rosowsky99th ed.New York Wiley-Interscience19721 online resource (982 p.)Chemistry of heterocyclic compounds ;v. 26Description based upon print version of record.9780471382102 0471382108 Includes bibliographical references.THE CHEMISTRY OF HETEROCYCLIC COMPOUNDS A SERIES OF MONOGRAPHS; Preface; Contents; Tables; I. Oxepins and Reduced Oxepins; A. OXEPINS; 1. Theoretical Interest; 2. Preparation; 3. Physical Properties; a. Infrared Absorption; b. Ultraviolet Absorption; c. Nuclear Magnetic Resonance; d. Thermodynamic Properties; 4. Chemical Reactions; a. Addendum; B. DIHYDROOXEPINS; 1. Introduction; 2. Preparation; 3. Physical Properties; a. Infrared Absorption; b. Ultraviolet Absorption; c. Nuclear Magnetic Resonance; 4. Chemical Reactions; C. TETRAHYDROOXEPINS; 1. Introduction; 2. Preparation3. Physical Propertiesa. Infrared Absorption; b. Nuclear Magnetic Resonance; 4. Chemical Reactions; D. HEXAHYDROOXEPINS (OXEPANS); 1. Preparation; a. Hexamethylene Oxide; b. Substituted Oxepans; (1) Ring Closure Reactions; (2) Ring Expansion Reactions; (3) Two-Component Reactions; 2. Physical Properties of Hexamethylene Oxide; 3. Chemical Reactions of Hexamethylene Oxide; 4. Preparation and Reactions of Cyclic Acetals, Ketals, and Related Compounds; E. TABLES; I-1. Oxepins and Reduced Oxepins; F. REFERENCES; II. Oxepin Ring Systems Containing Two Rings; A. FUSED RINGS SYSTEMS1. 2-Oxabicyclo[5.1.0]octanes2. 2-Oxabicyclo[5.2.0]nonanes; 3. 2H-Cyclopent[b]oxepins; 4. 2H-Cyclopent[d]oxepins; 5. Furo[3,4-b]oxepins; 6. Furo[3,4-d]oxepins; 7. 2H-Oxepino[2,3-b]pyrroles; 8. Thieno[3,4-d]oxepins; 9.1-Benzoxepins; a. Synthesis, Chemical Reactions, and Physical Properties of the Parent Compound; b. Synthesis and Chemical Reactions of Dihydro-l-benzoxepins; c. Synthesis and Chemical Reactions of Tetrahydro-l- benzoxepins; d. Synthesis and Chemical Reactions of Other Reduced 1-Benzoxepins; e. Physicochemical Properties of 2,3,4,5-Tetrahydro-1- benzoxepins; 10.2-Benzoxepins11. 3-BenzoxepinsB. SPIRANS; 1. 1,7-Dioxaspiro[5.6]dodecanes; 2. 1,4,6-Trioxaspiro[4.6]undecanes; C. BRIDGED SYSTEMS; 1. 2-Oxabicyclo[3.2.2]nonanes; 2. 3-Oxabicyclo[3.2.2]nonanes; 3. 9-Oxabicyclo[3.3.2]decanes; 4. 11-Oxabicyclo[4.4.1]undecanes; a. Partly or Fully Saturated Derivatives; b. 1,6-Oxido[10]annulenes; 5. 3-Oxa-6,7-dithiabicyclo[3.2.2]nonanes; D. TABLES; II-1. Uv Data and Bromination Rate of 2,3,4,5-Tetrahydro-l-benzoxepins and Lower Ring Homologs; II-2. Solvolysis Kinetics of 7-Chloromethyl-2,3,4,5-tetrahydro-l- benzoxepin and Lower Ring HomologsII-3. Uv Data and Bromination Rate of 2,3,4,5-Tetrahydro-l- benzoxepin-2-carboxylic Acid and Lower Ring HomologsII-4. Uv Data and Molecular Geometry of 2,3,4,5-Tetrahydro-2-(N,N-dimethylamino)methyl-1-benzoxepin Methobromide and Lower Ring Homologs; II-5. l-Benzoxepins; II-6. 2-Benzoxepins; II-7. 3-Benzoxepins; E. REFERENCES; III. Oxepin Ring Systems Containing Three Rings; A. FUSED RING SYSTEMS; 1. Cyclopenta[5.6]pyrano[4,3-b]oxepins; 2. 8H-1,3-Dioxolo[4,5-h][3]benzoxepins; 3. Dibenz[b,d]oxepins; 4. Dibenz[b,e]oxepins; 5. Dibenz[b,f]oxepins; 6. Dibenz[c,e]oxepinsa. Dibenz[c,e]oxepin-5,7-diones (Diphenic Anhydrides)Chemistry of Heterocyclic Compounds publishes articles, letters to the Editor, reviews, and minireviews on the synthesis, structure, reactivity, and biological activity of heterocyclic compounds including natural products. The journal covers investigations in heterocyclic chemistry taking place in scientific centers of all over the world, including extensively the scientific institutions in Russia, Ukraine, Latvia, Lithuania and Belarus.Chemistry of heterocyclic compounds ;v. 26.OxepinsThiepinsOxepins.Thiepins.547.592547/.59/05547/.592Rosowsky Andre93100MiAaPQMiAaPQMiAaPQBOOK9911020140303321Seven-membered heterocyclic compounds containing oxygen and sulfur4416821UNINA