Electron impact-induced decomposition of some substituted 7-ethoxycarbonylpyridopyrrolidenequinolines
✍ Scribed by Adam S. Plaziak; Tomasz Girek; Wanda Śliwa
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 241 KB
- Volume
- 27
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
The electron impact ionization mass spectrometric behaviour of three cycloadducts of 4,&benzo[ Llnaphthyridinum ethoxycarbonylmethylide with acrylonitrile, ethyl acrylate and diethyl maleate was studied with the aid of exact mass measurements and metastable transitions. The study showed that the electron impact-induced decomposition of substituted pyridopyrrolidenequinolines occurs exclusively on the aliphatic fivemembered ring.
📜 SIMILAR VOLUMES
The fragmentation behaviour of 18 vicinally substituted aminonitropyridines was studied under electron impact conditions. The decomposition patterns were found to be strongly dependent on the position of substituents The formation of the am analogue of carbazole seems phenylamioopyridine.