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in the presence of this alternate substrate, the reaction yields malonic acid semialdehyde, formaldehyde (akin to the action of histone demethylases), dimethylamine, and (1-methylimidazolidin-4-yl)acetic acid, "an unexpected product with an additional carbon-carbon bond resulting from N-demethylation coupled to oxidative rearrangement, likely via an unusual radical mechanism." [13] [12] The unusual mechanism is thought likely to involve a Steven's type rearrangement

Neuromuscular findings in thyroid dysfunction: a prospective clinical and electrodiagnostic study

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Oestreich LK, Pasternak O, Shenton ME, Kubicki M, Gong X, Australian Schizophrenia Research B, et al

Keistinen et al., 1997)