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Mass spectroscopy of natural products. XI—Mass spectroscopic investigations of N‐6 substituted ergoline derivatives
Author(s) -
Schmidt J.,
Seifert K.,
Härtling S.,
Johne S.,
Veith H. J.
Publication year - 1981
Publication title -
biomedical mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 0306-042X
DOI - 10.1002/bms.1200080105
Subject(s) - piperidine , chemistry , fragmentation (computing) , mass spectrometry , electron ionization , mass spectrum , spectroscopy , medicinal chemistry , stereochemistry , organic chemistry , chromatography , ion , computer science , ionization , physics , quantum mechanics , operating system
The fragmentation behaviour of N‐6 substituted ergoline derivatives (acylaminothiocarbonyl, thiazolyl) has been studied using electron impact, field desorption and collisional activation mass spectrometry. The specific fragmentations are compared with structurally related compounds (piperidine and piperidine‐3‐carboxylic acid methyl ester derivatives).