The behavior of phthalan (1a) was investigated under
conditions of electron transfer from alkali
metals in aprotic solvents. Reaction with lithium in the presence
of a catalytic amount of
naphthalene in THF led to the reductive cleavage of an arylmethyl
carbon−oxygen bond, with
formation of a stable dilithium compound. Trapping of this
intermediate with several electrophiles
(alkyl halides, carbonyl derivatives, CO2) was successful.
The extension of this procedure to several
substituted phthalans (1b
−
i) was
investigated, and the regiochemistry as well as the
synthetic
usefulness of these reactions are discussed.
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