Abstract
AbstractThe relative ratio of the dimers obtained by laccase‐catalyzed oxidation of tetrahydronaphthyl derivatives was profoundly influenced by the nature of the organic solvent used. For instance, in the oxidation of 5,6,7,8‐tetrahydronaphtalen‐2‐ol (1), the formation of the symmetrical 1,1′ product 1a with respect to the 1,3′ dimer 1b was highly favored in the aromatic solvents benzene and toluene.
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