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The fragmentation of 1-phenyl-2-propen-1-ol under electron impact
Authors:Jean-Pierre Denhez  Madeleine Corval  Pierre Dizabo
Abstract:The electron impact mass spectra of 1-phenyl-2-propen-1-ol and its specifically deuterated analogues have been investigated. Most of the decomposition pathways involve skeletal rearrangements or hydrogen atom transfers, such that a rearrangement of the excited molecular ions of 1-phenyl-2-propen-1-ol to molecular ions of cinnamic alcohol and/or cinnamaldehyde can be anticipated.
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