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ChemInform Abstract: cyclo‐Trimerization of 1,4‐Naphthoquinone; Cooperation of Phenol/Quinone Additions and Redox Reactions.

HANS JUN. BROCKMANN

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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).

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Available 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).

Key concepts: Chemistry, Quinone, Hydroquinone, Naphthoquinone, 1,4-Naphthoquinone, Redox, Phenol, Medicinal chemistry

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ChemInform Abstract: cyclo‐Trimerization of 1,4‐Naphthoquinone; Cooperation of Phenol/Quinone Additions and Redox Reactions. — Research Paper | ScholarLens