Fast atom bombardment mass spectrometry of some penicillins
β Scribed by Michael Barber; Robert S. Bordoli; R. Donald Sedgwick; Andrew N. Tyler; Brian N. Green; Victor C. Parr; John L. Gower
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 359 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
β¦ Synopsis
The new technique of fast atom bombardment mass spectrometry has been applied to the investigation of a series of penicillins as free acids or as alkali metal salts. In all cases both positive and negative ion pseudomolecular species are observed giving molecular weight information. Additionally, significant fragmentation is observed in both the positive and negative ion spectra, which gives considerable structural information.
π SIMILAR VOLUMES
A new series of thymine derivative acyclic nucleosides, with mono-or polyfluorosubstitution on the acyclic portion of the molecules have been studied by fast-atom bombardment mass spectrometry, with the aid of metastable ion studies and deuterium labelling experiments. The protonated molecules show
Three glutathione conjugates of acetaminophen were characterized by fast atom bombardmentlmass spectrometry (FABlMS) and fast atom bombardmentlmass spectrometryhass spectrometry (FABlMSlMS). The conjugates, 3-(glutathion-S-yl)acetaminophen, 3-(glutathion-S-yl)diacetaminophen and 3-(diglutathion-S-yl
The positive-ion fast-atom bombardment (FAB) mass spectra of 23 zearalenone derivatives have been obtained and structures for the ion fragments were proposed. Careful analysis of the FAB spectra obtained for these derivatives, accurate mass measurement and MS/MS experiments for zearalenone, 3'-oxoze