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Synthesis of 6H-Naphtho[1,2,3-cd]indol-6-ones.

✍ Scribed by L. M. Gornostaev; V. A. Beresnev; T. I. Lavrikova; I. L. Mezrina

Publisher
John Wiley and Sons
Year
2004
Weight
13 KB
Volume
35
Category
Article
ISSN
0931-7597

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## Abstract Der Thioxanthenyl‐glycinester **2b** cyclisiert in Acetanhydrid/Natriumacetat zu den Benzothiopyrano[4,3,2‐cd]indolen **4c** und **4d**, in Γ„thanol/Natriumalkoholat zu dem Indolin **3** und dem Indol **4e**. Aus **4c** und **4e** entsteht nach Hydrolyse und Decarboxylierung das Indol **