The electron impact ionization and collisional activation mass spectra of a-phenylcinnamic acid and its derivatives have been studied. The loss of a phenylic hydrogen is not an important process in these molecules, unlike the unsubstituted cinnamic acids. However, in o-chloro-a-phenylcinnamic acid a
Labelling studies of hydrogen rearrangements in the chemical ionization mass spectra of cyclohexanone and its derivatives
β Scribed by Vladimir Diakiw; Robert J. Goldsack; James S. Shannon; Michael J. Lacey
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 682 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1076-5174
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