A novel formation of the indole derivatives by phenolic oxidative coupling
β Scribed by Tetsuji Kametani; Isao Noguchi; Kiyosato Nyu; Seiichi Takano
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 173 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Tine photochemically induced formation of N-acetyl-2nydroxy-2,3\_dihydroindoles (XII, R1 = CHS) in tautomeric equilibrium with the corresponding oxo-compounds (XI, Rl = CHS), from a series of 2-methylquinoline N-oxides (V), has recently been described (1;2). We wish to report that a similar reaction
Ferricynnide oxidation of the dianion of the pbenolic B-diketone 6b in basic conditions effects intramolecular radical coupling to form the spirocyclic diketone I which leads to the hydroxy tetralone 8 via an oxidative fragmentation process. \_ Reactions in Steroid Chemistry",