Liebigs Annalen der Chemie

Dimere Naphthochinone, IX. Isodiospyrin und Elliptinon.—Synthese 6, 6′??dimerer Bijuglone durch Phenoloxidation

H Laatsch

Index: Laatsch, Hartmut Liebigs Annalen der Chemie, 1984 , # 2 p. 319 - 339

Full Text: HTML

Citation Number: 5

Abstract

Abstract Durch oxidative Kupplung des Naphthols 37b wurde der potentielle Naturstoff 7, 7′-Dimethyl-6, 6′-bijuglon (5) und in kleinerer Ausbeute Isodiospyrin (21) erhalten. Regiospezifische Synthesen von 5, Elliptinon (10) und 6, 6′-Bijuglon (45a) gelangen durch Phenoloxidation geeignet substituierter p-Chlornaphthole.

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