## Abstract The mass spectrometric behaviour of the 1,3‐diaminopropane derivative **4a** (3,7‐diacetyl‐3,7‐diazadodecane) was investigated with regard to the fragmentation reactions of N, N′, N″‐triacetylspermidine (**1**), as model for the 1,3‐diaminopropane part. It was established that the degra
Nachbargruppenbeteiligung bei massenspektrometrischen Fragmentierungsreaktionen: Spermin-Derivate. 18. Mitteilung über das massenspektrometrische Verhalten von Stickstoffverbindungen
✍ Scribed by E. Schöpp; Manfred Hesse
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- German
- Weight
- 869 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The mass spectral behaviour of tetraacetyl spermine (2) has been investigated. The fragmentation reactions are characterized by the neighbouring group participation of the amide nitrogen atoms. Only a few reactions can be explained by usual pathways (α‐cleavage, onium reactions). Most of the fragment‐ions are formed by neighbouring group participation:
[M‐COCH~3~]^+^‐Ion.
Breakdown of one of the two 1,3‐diaminopropan moieties: m/e 242, 256, 268. This type of fragmentation is characteristic for all acetylated 1,3‐diaminopropan‐derivatives e.g. triacetylspermidine.
Expulsion of a neutral amine: m/e 169.
S~N~i‐type reactions, by which cyclic ions are formed: m/e 100.
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