ChemInform Abstract: STUDIES ON 1‐AZABICYCLO COMPOUNDS PART 19, SYNTHESIS OF TEN‐MEMBERED RING AMINE DERIVATIVES FROM 5‐METHYL‐10‐NITROMETHYLOCTAHYDROQUINOLIZINIUM IODIDE AND ITS DERIVATIVES

Arata, Yoshio; Kikuti, Tetuo; Takahashi, M.; Aoki, Tsutomu

doi:10.1002/chin.197437293

Chemischer Informationsdienst

1974

DOI: 10.1002/chin.197437293

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ChemInform Abstract: STUDIES ON 1‐AZABICYCLO COMPOUNDS PART 19, SYNTHESIS OF TEN‐MEMBERED RING AMINE DERIVATIVES FROM 5‐METHYL‐10‐NITROMETHYLOCTAHYDROQUINOLIZINIUM IODIDE AND ITS DERIVATIVES

Yoshio Arata¹,

Tetuo Kikuti²,

M. Takahashi³

et al.

Abstract: Das Hexahydrochinolizin (I) reagiert mit Nitromethan und Methyljodid in Methanol bei 0°C unter Stickstoff in Abhängigkeit von den molaren Verhältnissen zu 5‐Methyl‐ 10‐nitromethyloctahydrochinoliziniumjodid (II) und zum Chinoliziniunrsalz (III).

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ChemInform Abstract: STUDIES ON 1‐AZABICYCLO COMPOUNDS PART 19, SYNTHESIS OF TEN‐MEMBERED RING AMINE DERIVATIVES FROM 5‐METHYL‐10‐NITROMETHYLOCTAHYDROQUINOLIZINIUM IODIDE AND ITS DERIVATIVES

Abstract: Das Hexahydrochinolizin (I) reagiert mit Nitromethan und Methyljodid in Methanol bei 0°C unter Stickstoff in Abhängigkeit von den molaren Verhältnissen zu 5‐Methyl‐ 10‐nitromethyloctahydrochinoliziniumjodid (II) und zum Chinoliziniunrsalz (III).

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References 1 publication

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