Abstract
The mass spectrometric behaviour of seven neuroleptic amino alkyl thieno[β]cycloalkanones has been studied under electron ionization conditions and with the aid of metastable ion studies, low energy collisional experiments and accurate mass measurements. The most relevant fragmentation pathways are discussed and the power of the different methodologies for the characterization of structural isomers has been tested. © 1998 John Wiley & Sons, Ltd.
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