作者:Maximilian Gutsche、Dominik Pfaff、Joachim Podlech
DOI:10.1002/ejoc.202301052
日期:2024.1.15
The core of the perylenequinone-derived mycotoxin altertoxin I was synthesized either from 3-hydroxyacetophenone or from 1,5-dihydroxynaphthalene, where Suzuki couplings, Ullmann couplings, McMurry olefinations, and Friedel-Crafts acetylation were key steps in the respective syntheses.
苝醌衍生的霉菌毒素 I 的核心是由 3-羟基苯乙酮或 1,5-二羟基萘合成的,其中 Suzuki 偶联、Ullmann 偶联、McMurry 烯化和 Friedel-Crafts 乙酰化是各自合成中的关键步骤。