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Isoxazoles . Part one [[electronic resource] /] / Paolo Grünanger, Paola Vita-Finzi



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Autore: Grünanger Paolo Visualizza persona
Titolo: Isoxazoles . Part one [[electronic resource] /] / Paolo Grünanger, Paola Vita-Finzi Visualizza cluster
Pubblicazione: New York, : John Wiley & Sons, 1991
Descrizione fisica: 1 online resource (904 p.)
Disciplina: 547.592
547/.59/05
547/.592
Soggetto topico: Oxazoles
Chemistry
Soggetto genere / forma: Electronic books.
Altri autori: Vita-FinziPaola  
DowlingJames Edward <1966->  
Note generali: Description based upon print version of record.
Nota di bibliografia: Includes bibliographical references and indexes.
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
Sommario/riassunto: Isoxazoles. Isoxazolines (Dihydroisoxazoles). Isoxazolidines (Tetrahydroisoxazoles). References. Index.
Titolo autorizzato: Isoxazoles  Visualizza cluster
ISBN: 1-282-30723-1
9786612307232
0-470-18735-2
0-470-18887-1
Formato: Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione: Inglese
Record Nr.: 9910144286003321
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Serie: Chemistry of heterocyclic compounds ; ; v. 49.