Abstract
AbstractBei der Oxidation von Isoeugenol (II) mit dem Tri‐tert.‐butylphenoxyl‐Radikal [in situ aus dem Phenol (I)] werden vier trimere Oxidationsprodukte (IIIa), (IIIb), (IV) und (V) erhalten, deren Strukturen anhand eingehender Untersuchung der PMR‐ und Massenspektren geklärt werden.
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