Abstract
Cationic electrocyclization of α-benzoyldiphenylmethanols in the presence of superacid
provides fluorenes, phenanthrols and benzofurans in good to moderate yields. A single
substitution leads to regioselective cationic electrocyclizations.
Key words
carbocations - electrocyclizations - regioselectivity - superacid - diphenylmethyl
cations
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