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- W2328668346 abstract "Die Nitroindole (I) reagieren in Gegenwart von Benzyltrimethylammoniumhydroxid mit Acrylnitril (II) zu den cyanäthylierten Verbindungen (III), die durch Hydrierung über Raney-Nickel zu den Aminopropylderivaten (IV) und durch Hydrolyse mit wäßriger Kalilauge in die Carbonsäuren (V) umgewandelt werden." @default.
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- W2328668346 date "1973-05-01" @default.
- W2328668346 modified "2023-09-26" @default.
- W2328668346 title "ChemInform Abstract: DIE CYANAETHYLIERUNG VON NITROINDOLEN" @default.
- W2328668346 doi "https://doi.org/10.1002/chin.197318282" @default.
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