Electron impact mass spectra of 5,5-bis(carboethoxy)-1,3-dioxanes
β Scribed by Mihai Horn; Sorin Mager; Nicolae Palibroda; Monica Culea
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 255 KB
- Volume
- 26
- Category
- Article
- ISSN
- 1076-5174
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β¦ Synopsis
Electron impact-induced fragmentations of 2-substituted 5,5-bis(carboethoxy)l,3-dioxanes were studied by exact mass measurements and metastable ion analysis. The substituent R on C(2) of the heterocyclic ring has little influence on the principal cleavage reactions. Elimination of CH,O/CO and C,H,O/C,H,/C,H,OH are common fragmentations for ions containing the 1,Mioxane moiety or the OC,H, group, respectively. The abundant ions at m/z 173 and 127 serve as structural probes for the class of compounds studied. Primary fragmentations implying the ester function are of little importance.
π SIMILAR VOLUMES
## Abstract The positions of conformational equilibria in a variety of 5,5βdisubstituted 1,3βdioxans have been established by lowβtemperature ^1^H and ^13^C NMR spectroscopy and by reference to the NMR spectra of anancomeric 2,5,5βtrisubstituted derivatives.
Fragmentation pathways of the title compounds under electron impact were compared to those of their (1aryl)substituted analogs reported earlier. The main fragmentation route of the M Γ ions is the sulphamide N-S bond cleavage leading to [M Γ ArSO 2 ] ions. No loss of the alkyl substituents from the