Chemischer Informationsdienst. Organische Chemie
 1971
DOI: 10.1002/chin.197128276
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ChemInform Abstract: UNTERSUCHUNGEN AN HETEROCYCLISCHEN CHINONEN 15. MITT. SYNTHESE UND ANTIMIKROBIELLE WIRKUNG SUBSTITUIERTER 4,5‐INDOLOCHINONE

A. V. Luk'yanov1,
É. A. Rudzit2,
V. A. Aleshina3
et al.

Abstract: Die S‐Hydroxyindole (I) lassen sich in Mischungen aus Piperidin und Methanol in Gegenwart katalytischer Mengen Kupferacetat mit Sauerstoff zu den 4,5‐Indolochinonen (II) oxidieren (70‐74% Ausbeute) und weiter mit o‐Phenylendiamin in 69 ‐ 84%iger Ausbeute zu den Phenazinen (III) kondensieren.

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