Radical-cation-mediated oxidation of 9-methylanthracene (9MA) by
pyridine/iodine in chloroform
produces mainly the product of nucleophilic attack at the open C-10
position. When methyl is
replaced by ethyl as in 9-ethylanthracene (9EA), the nucleophilic
product is the only one observed.
Alternatively, aceanthrene (AA), the 1,9-ethano-bridged equivalent
of 9EA, produces mainly the
product of side-chain substitution. Stereoelectronic control in
the deprotonation is proposed as
the rationale for this difference in reactivity, as well as for other
radical-cation-mediated oxidations.
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