期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 80, 期 20, 页码 10033-10040出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.5b01634
关键词
-
资金
- Fundacao de Amparo a Pesquisa do Estado de Sao Paulo, Brazil (FAPESP)
- CAPES
- FAPESP
Total syntheses of lysicamine, (+/-)-nuciferine, (+/-)-nomuciferine, (+/-)-zanthoxyphylline iodide, (+/-)-O-methylisothebaine, and (+/-)-trimethoxynoraporphine were accomplished by an approach that involves the formation of aporphine cores through reactions between an isoquinoline derivative and silylaryl triflates promoted by CsF. Unprecedented formations of aporphine cores proceeded in good yields presumably through [4 + 2] cycloaddition reactions followed by hydrogen migrations.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据