The mass spectrometric behaviour of three 1a,3-diaryl-1,1,4,4-tetrachloro-1a,2,3,4-tetrahydro-1H-azirino [2,1-e][1,6]benzothiazocines has been studied with the aid of mass-analyzed ion kinetic energy spectrometry and exact mass measurements under electron impact ionization. All compounds show a tend
Mass spectral fragmentation patterns of new 5-acetyl-4-aryl-6-methyl-2(1H)pyridones
โ Scribed by Roberto Martinez; Margarita Suarez; Nazario Martin; Estael Ochoa; Carlos Seoane; Yamila Verdecia
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 36 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0951-4198
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โฆ Synopsis
The electron impact mass spectra of new 5-acetyl-4-aryl-6-methyl-2(1H)pyridones have been studied. A dominant peak in all the spectra is due to cleavage of the CO-NH bond of the amido group with charge retention on the carbonyl group. This fragmentation is followed by a hydrogen rearrangement to the nitrogen atom forming ketene intermediates; this pathway leads to a highly stabilized ion which constitutes the base peak in the spectra in most of the compounds studied.
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