Hussain Hidayat, Aziz Shahid, Schulz Barbara, Krohn Karsten
Department of Chemistry, Universität Paderborn, Warburger Strasse 100, 33098 Paderborn, Germany.
Nat Prod Commun. 2011 Jun;6(6):841-3.
The five-step synthesis of the new 4H-anthra[1,2-b]pyran derivative 1 is reported. The key steps in this approach included a Marschalk alkylation of 1,4-dihydroxyanthraquinone followed by a Baker-Venkataraman reaction and then an acid-catalyzed cyclization of ring A to form the 4H-anthra[1,2-b]pyran system. Two compounds, the 4H-anthra[1,2-b]pyran 1 and the anthraquinone derivative 6 were evaluated for antimicrobial activity and showed moderate antialgal, antifungal, and antibacterial activities.
报道了新型4H-蒽[1,2-b]吡喃衍生物1的五步合成方法。该方法的关键步骤包括1,4-二羟基蒽醌的马尔沙克烷基化反应,随后进行贝克-文卡塔拉曼反应,然后对A环进行酸催化环化以形成4H-蒽[1,2-b]吡喃体系。对两种化合物,即4H-蒽[1,2-b]吡喃1和蒽醌衍生物6进行了抗菌活性评估,结果显示它们具有中等程度的抗藻、抗真菌和抗菌活性。