Abstract
AbstractDie alkalische Oxidation von 2,6‐Di‐tert.‐butylphenolen (I) liefert je nach Art des Substituenten R in 4‐Stellung unterschiedliche Derivate wie Semichinone (II), Phenolaldehyd (III), Ester (IV) bzw. Azabicyclo‐dien‐dion (V) sowie spirocyclische Derivate wie (VI).
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