药根碱
黄连碱
小檗碱
化学
巴马汀
分子内力
弗里德尔-克拉夫茨反应
有机化学
组合化学
立体化学
催化作用
作者
Luis M. Mori‐Quiroz,Sidnee L. Hedrick,Andrew R. De Los Santos,Michael D. Clift
出处
期刊:Organic Letters
[American Chemical Society]
日期:2018-06-28
卷期号:20 (14): 4281-4284
被引量:37
标识
DOI:10.1021/acs.orglett.8b01702
摘要
Total syntheses of the antibacterial alkaloids berberine, coptisine, and jatrorrhizine have been achieved in four steps through a unified route. The key step of this strategy is an efficient intramolecular Friedel-Crafts alkoxyalkylation which, following oxidation, establishes the isoquinolinium core of these natural products. Herein, the design and development of this synthetic strategy, which has enabled the shortest and most efficient syntheses of these alkaloids reported to date, is described.
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