Geometric and positional isomers of the A\*-oxazoline ring system have been characterized by their mass spectral fragmentation patterns. The composition of the major ions in the spectra have been determined by high resolution mass spectrometry. A fragmentation pathway for the formation of these ions
The mass spectrometry of 2-methylthio(glyco)oxazoline derivatives of pentoses and hexoses
โ Scribed by Gary D. Byrd; Robert M. Davidson; White V Edward; Bruce Coxon; Sam A. Margolis
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 314 KB
- Volume
- 20
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
โฆ Synopsis
The fragmentation of 2-methylthio(glyco)oxazolines under electron impact has been investigated by low-and high-resolution mass spectrometry. Field desorption was used in those cases where the molecular ion was weak or missing. Fragmentation pathways were determined by monitoring metastable transitions and through the use of labeled compounds. The results support the anticipated structure for these compounds and show the sensitivity of the mass spectra toward ring size.
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