Polyalkoxy-substituted nitrostilbenes in the synthesis of lamellarin analogs. Formal synthesis of lamellarin H
RUSSIAN CHEMICAL BULLETIN(2023)
Abstract
Lamellarin D trimethyl ether was prepared by 1,3-dipolar cycloaddition of 6,7-dimethoxyisoquinolinium ylide to pentamethoxy-substituted nitrostilbene followed by a lactone ring closure in the intermediate cycloadduct. This approach allowed a formal synthesis of lamellarin H.
MoreTranslated text
Key words
essential oils,Acorus calamus,azarone,isoquinolinium ylides,nitrostilbenes,1,3-dipolar cycloaddition,lamellarin D trimethyl ether,lamellarin H,formal synthesis
AI Read Science
Must-Reading Tree
Example
![](https://originalfileserver.aminer.cn/sys/aminer/pubs/mrt_preview.jpeg)
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined