Synthesis, characterization and electron impact mass spectrometry of Schiff bases rearranging to oxazoline, thiazoline and thiazole derivatives (Articolo in rivista)

Type
Label
  • Synthesis, characterization and electron impact mass spectrometry of Schiff bases rearranging to oxazoline, thiazoline and thiazole derivatives (Articolo in rivista) (literal)
Anno
  • 1988-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/jhet.5570250121 (literal)
Alternative label
  • Guerriero P.; Bullita E.; Vigato P. A.; Pelli B.; Traldi P. (1988)
    Synthesis, characterization and electron impact mass spectrometry of Schiff bases rearranging to oxazoline, thiazoline and thiazole derivatives
    in Journal of heterocyclic chemistry (Online); John Wiley & Sons Ltd., Chichester (Regno Unito)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Guerriero P.; Bullita E.; Vigato P. A.; Pelli B.; Traldi P. (literal)
Pagina inizio
  • 145 (literal)
Pagina fine
  • 154 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://onlinelibrary.wiley.com/doi/10.1002/jhet.5570250121/abstract (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 25 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 10 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 1 (literal)
Note
  • Wiley OnLine Library (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • 1-3 : Istituto di Chimica e Tecnologia dei Radioelementi -- C.N.R.-, Area della Ricerca, C.so Stati Uniti, 4 Padova, Italy / 4-5 : C.N.R.-, Area della Ricerca, C.so Stati Uniti, 4 Padova, Italy (literal)
Titolo
  • Synthesis, characterization and electron impact mass spectrometry of Schiff bases rearranging to oxazoline, thiazoline and thiazole derivatives (literal)
Abstract
  • A series of oxazoline compounds have been prepared by reaction of 2,6-diformyl-4-chlorophenol, 2,6-diformylpyridine or 2,5-diformylthiophen with o-aminophenol or o-aminothiophenol respectively. The oxazoline derivatives are stable both in solid state and in solution while the thiazoline derivatives easily oxidize to the corresponding thiazoles. Physico-chemical data confirm this oxidation process. The 70 eV electron impact induced decomposition pathways of these compounds, obtained with the aid of exact mass measurements, B/E linked scans and collisional spectroscopy, are discussed in detail. (literal)
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