杂环化合物的合成研究。CCCLXXXVI一部分。加兰他敏和n -苄基碘化加兰他敏的替代全合成

T. Kametani, C. Seino, K. Yamaki, S. Shibuya*, K. Fukumoto*, K. Kigasawa, F. Satoh, M. Hiiragi, T. Hayasaka
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引用次数: 16

摘要

加兰他敏(Ia)和n -苄基加兰他敏碘化(VIa)通过相应的酰胺(IIIf和e)的酚氧化反应进行替代全合成。(-)和(±)-加兰他敏均表现出与吗啡相当的镇痛活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies on the syntheses of heterocyclic compounds. Part CCCLXXXVI. Alternative total syntheses of galanthamine and N-benzylgalanthamine iodide
Alternative total syntheses of galanthamine (Ia) and N-benzylgalanthamine iodide (VIa) were carried out by phenolic oxidative reactions of the corresponding amides (IIIf and e). Both (–)-and (±)-galanthamine showed analgesic activity comparable to that of morphine.
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