Chemischer Informationsdienst. Organische Chemie
 1970
DOI: 10.1002/chin.197015397
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ChemInform Abstract: SYNTHETHISCHE ARBEITEN IN DER REIHE DER ERYTHRINA‐ALKALOIDE 11. MITT. ANWENDUNG DER GLYOXYLESTER‐SYNTH.

Albert Mondon1,
Karl Fr. W. Hansen2,
Klaus Boehme3
et al.

Abstract: Die Kondensation der Ester (I) (dargestellt aus den entsprechenden 4‐substituierten Cyclohexanonen und Oxalsäurediäthylester = Glyoxylestersynthese) mit dem Amin (II) liefert die Oxindole (III) (40‐69% Ausbeute).

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