Abstract
A specific para hydroxylation of the aromatic ring of isopropyl N-phenyl carbamate 1 by the fungus Beauveria sulfurescens has been achieved. Studies of the deuterium labelled compound show high retention (NIH shift) for this transformation, a fact uhich indicates that the mechanism implied is consistent which the intermediate formation of an arene oxide. Also, formation of a glucoside conjugate of the phenol has been observed.
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