ChemInform Abstract: Die Stereochemie von Stickstoff‐Heterocyclen. 48. Mitt. Synthese, Konfiguration und IR‐Spektren von 1,2‐Dimethyldecahydrochinololen‐5 und ihren Acetaten.

Litvinenko, G. S.; Kuz'mina, N. Yu.; Sokolov, D. V.

doi:10.1002/chin.198432220

Chemischer Informationsdienst

1984

DOI: 10.1002/chin.198432220

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ChemInform Abstract: Die Stereochemie von Stickstoff‐Heterocyclen. 48. Mitt. Synthese, Konfiguration und IR‐Spektren von 1,2‐Dimethyldecahydrochinololen‐5 und ihren Acetaten.

G. S. Litvinenko¹,

N. Yu. Kuz'mina²,

D. V. Sokolov³

Abstract: Die Methyldecahydrochinolole (Ia)‐(IIIa) werden mit Formalin und Ameisensäure zu den N‐Methylderivaten (Ib)‐(IIIb) alkyliert und diese mit Acetylchlorid oder Acetanhydrid in die Acetate (Ic)‐(IIIc) umgewandelt.

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ChemInform Abstract: Die Stereochemie von Stickstoff‐Heterocyclen. 48. Mitt. Synthese, Konfiguration und IR‐Spektren von 1,2‐Dimethyldecahydrochinololen‐5 und ihren Acetaten.

Abstract: Die Methyldecahydrochinolole (Ia)‐(IIIa) werden mit Formalin und Ameisensäure zu den N‐Methylderivaten (Ib)‐(IIIb) alkyliert und diese mit Acetylchlorid oder Acetanhydrid in die Acetate (Ic)‐(IIIc) umgewandelt.

This publication either has no citations yet, or we are still processing them

See others like this or search for similar articles

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