Synthesis and mass spectra of some aryl aldehyde thiosemicarbazones
Egyptian Journal of Chemistry. 2005; 48 (6): 695-714
Dans Anglais
| IMEMR
| ID: emr-70483
ABSTRACT
The reaction of ethyl beta-aryl-alpha-cyanoacrylate [1] with thiosemicarbazide in the presence of potassium carbonate gave arylaldehydethiosemicarbazone [3]. Treatment of compound 3 with acetic anhydride, benzoyl chloride and ethyl chloroacetate yielded the corresponding 4-[substituted benzaldehyde-2, 4-diacetytl hiosemicarbazone] [4], 4 [substituted benzaldehyde -2, 4-dibenzoyl thiose micarbazones] [5], and 3-substituted-2-thioxo-imidazolidin-4-one [6]. The mass spectral fragmentation patterns of the compounds 3, 4, 5 and 6 are described
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Indice:
Méditerranée orientale
Sujet Principal:
Spectrométrie de masse
langue:
Anglais
Texte intégral:
Egypt. J. Chem.
Année:
2005
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