Abstract
Collision-induced dissociation (CID) of lithiated molecules generated by liquid SIMS (LSIMS) from two new natural compounds, annoheptocin A and B, led to their structural elucidation. Mass spectrometry (MS) and tandem mass spectrometry (MS/MS) investigations of their acetonide derivatives displayed obvious differences of reactivity of the lithiated dioxane and dioxolane rings towards CID. The 1,3-dioxane (six-membered) ring could be the target of hydrogen rearrangement processes, leading to the formation of a tetrahydrofuran ring through the loss of a molecule of acetone. Copyright © 1998 John Wiley & Sons, Ltd.
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