The mass spectral fragmentation pathways of 1-alkyl-5-bromo-4-hydroxypyridazin-6-ones were studied under electron ionization by means of low resolution, high resolution and metastable ion analysis techniques. The principal fragmentation pathways of these compounds involved various skeletal rearrange
Mass Spectrometric Fragmentation of Saturated Isoindolobenzoxazepinones and -benzoxazinones Under Electron Ionization
✍ Scribed by Tuula Partanen; Pirjo Vainiotalo; Géza Stájer; Gábor Bernáth
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 423 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0951-4198
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✦ Synopsis
The mass spectral fragmentation of three isoindolo[2,4]benzoxazepinones, five isoindolo[3,11-and two isoindolo[l,3]benzoxazinones was studied under electron ionization by means of low-resolution, high resolution and metastable-ion analysis techniques. The major fragmentation pathways began as radical-site-initiated cleavage, and ionization of the nitrogen atom seemed to prevail. Ionization of the carbonyl and heterocyclic oxygen atoms was also observed. For the trinorbornene compound, a retro-Diels-Alder reaction was favoured.
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