ChemInform Abstract: cyclo‐Trimerization of 1,4‐Naphthoquinone; Cooperation of Phenol/Quinone Additions and Redox Reactions.
HANS JUN. BROCKMANN
Abstract
HANS JUN. BROCKMANN
Abstract
Abstract The reaction course previously postulated for the cyclo‐trimerization of 1,4‐naphthoquinone (I) to cyclo‐tri‐1,4‐naphthoquinone (III) is confirmed and supplemented by: a) isolation of the red intermediate (V), b) synthesis of (III) starting from (V) or the compound (VI), a further intermediate, and c) reduction of (V) and (VI) by (II) to the bis‐hydroquinone (IV).
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Abstract The reaction course previously postulated for the cyclo‐trimerization of 1,4‐naphthoquinone (I) to cyclo‐tri‐1,4‐naphthoquinone (III) is confirmed and supplemented by: a) isolation of the red intermediate (V), b) synthesis of (III) starting from (V) or the compound (VI), a further intermediate, and c) reduction of (V) and (VI) by (II) to the bis‐hydroquinone (IV).
Key concepts: Chemistry, Quinone, Hydroquinone, Naphthoquinone, 1,4-Naphthoquinone, Redox, Phenol, Medicinal chemistry