Abstract:N‐Substituted dihydro‐1,3,5‐dioxazines show a general fragmentation pattern supported by metastable ions, exact mass measurements and deuterium labelling. There are two well‐defined pathways: one is initiated by elimination of the N‐substituent and the other by loss of a hydrogen atom from the heterocyclic ring.
The mass fragmentation behaviour of 3,4-dihydro-lH-2,3-benzothiazine 2,2-dioxides was studied. The rationalizations suggested are supported by accurate mass measurements, metastable evidence and deuterium labelling.
The mass fragmentation behaviour of 3,4-dihydro-lH-2,3-benzothiazine 2,2-dioxides was studied. The rationalizations suggested are supported by accurate mass measurements, metastable evidence and deuterium labelling.
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