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- W2606422384 abstract "Die katalytische Debenzylierung des Dimethylaminoindols (Ia) in Methanol liefert neben dem Hydroxyindol (II) (Ausbeute 69% bei Anwendung von 2 Mol- Aquivalenten H2) noch das Oxoindol (III) (5-40%, je nach Hydrierungsdauer), wahrend das Methylindol (Ib) [aus (Ia) mit CH3J ; 87%] von Hz/Pd selektiv zu (II) umgesetzt wird (93%)." @default.
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- W2606422384 date "1972-02-22" @default.
- W2606422384 modified "2023-09-27" @default.
- W2606422384 title "ChemInform Abstract: SYNTHETISCHE INDOLVERBINDUNGEN 10. MITT. CHEMIE DER 4-HYDROXY-INDOL-VERBINDUNGEN" @default.
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- W2606422384 doi "https://doi.org/10.1002/chin.197208244" @default.
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