Abstract
Incubation of N-benzoyl- and 1-methyl-N-benzoyl-1,2,3,4-tetrahydroisoquinolines with the mycelium of the fungus Cunninghamella elegans results in both benzylic hydroxylation and the formation of phenolic products; the 2- and 3-methyl substituted analogues gave products arising from C-1 hydroxylation.
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