期刊
ORGANIC LETTERS
卷 21, 期 17, 页码 7033-7037出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b02613
关键词
-
资金
- NSFC [21971093]
- Fundamental Research Funds for the Central Universities [lzujbky-2018-62]
- International Joint Research Centre for Green Catalysis and Synthesis, Gansu Provincial Sci. & Tech. Department [2016B01017, 18JR3RA284, 18JR4RA003]
- Lanzhou University
- E.B. Eddy endowment fund
Phenols are readily available by degradation of lignin resource. Palladium-catalyzed conversion of phenols to tetrahydro-beta-carboline skeletons bearing a spirocycle at the C-1 position in water is reported. Various substituted phenols are successfully cross-annulated with different tryptamines via sequential C(Ar)-O bond cleavage of phenols, C-H bond activation of tryptamines, and C-N/C-C bond formations. This method provides a new protocol of converting lignin phenols into high-value-added compounds, such as natural product Komavine.
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