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- W2344146883 abstract "Indol (I) wird in Methylenchlorid mit gepulvertem Natriumhydroxid in Gegenwart von Tetrabutylammonium-hydrogensulfat in guten Ausbeuten selektiv in Position 1 zu (III) acyliert." @default.
- W2344146883 created "2016-06-24" @default.
- W2344146883 creator A5047090520 @default.
- W2344146883 date "1979-08-28" @default.
- W2344146883 modified "2023-09-26" @default.
- W2344146883 title "ChemInform Abstract: PHASE-TRANSFER CATALYZED N-ACYLATION OF INDOLE" @default.
- W2344146883 cites W2042974383 @default.
- W2344146883 doi "https://doi.org/10.1002/chin.197935214" @default.
- W2344146883 hasPublicationYear "1979" @default.
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