Mass spectrometry in structural and stereochemical problems—CCIV. Spectra of hydantoins II. Electron impact induced fragmentation of some substituted hydantoins
- 1 May 1971
- journal article
- research article
- Published by Wiley in Journal of Mass Spectrometry
- Vol. 5 (5) , 551-563
- https://doi.org/10.1002/oms.1210050507
Abstract
The mass spectral decomposition modes of hydantoin and derivatives containing alkyl and phenyl substituents have been investigated using isotopic labeling techniques. The loss of carbon monoxide from the molecular ions of these compounds was shown to preferentially involve the C‐4 carbonyl group. Other fragmentation processes characteristic of the hydantoin ring system and the effect on this of alkyl and phenyl substitution are described.Keywords
This publication has 8 references indexed in Scilit:
- The mass spectra of succinimides, hydantoins, oxazolidinediones and other medicinal anti-epileptic agentsJournal of Mass Spectrometry, 1970
- Spectres de Masse d'Imides CycliquesBulletin des Sociétés Chimiques Belges, 1969
- Identification of Medicinal Barbiturates by Means of Mass SpectrometryJournal of Pharmaceutical Sciences, 1968
- Localization of substituents in the hydantoin ring by nuclear magnetic resonanceSpectrochimica Acta, 1965
- Massenspektroskopie in der DrogenanalyseMonatshefte für Chemie / Chemical Monthly, 1965
- Mass Spectrometry in Structural and Stereochemical Problems. LXX.1 A Study of the Fragmentation Processes of Some Five-Membered N-Alkyllactams and N-Alkylsuccinimides2Journal of the American Chemical Society, 1965
- Mass Spectrometric Analysis. Molecular RearrangementsAnalytical Chemistry, 1959
- The Chemistry of the Hydantoins.Chemical Reviews, 1950