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product are Fe(III)BLM and the 4
aldehyde lesion mentioned above [reac-
tion (52)]. For a further reaction, the Fe(III)BLM has to be reactivated.
′
keto-1
′
The formation of base propenals is not as straight-forward. From the above, it
is clear that O
2
is required for the formation of the base propenals. After the
formation of the
C
(4
) peroxyl radical [reaction (53)], the Fe(IV)BLM species
has to interact with this peroxyl radical, possibly by forming an adduct [reaction
(54)]. The latter then decomposes and subsequently yields the products, the 3
′
-
′
phosphoglycolate, the base propenal and the 5
-phosphate terminus [reactions
(55)−(57)]. When reaction (53) is carried out with
18
O
2
,
18
O is incorporated into
the 3
′
-phosphoglycolate (McGall et al. 1987), while the carbonyl oxygen of the
′
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