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首页> 外文期刊>Journal of the Brazilian Chemical Society >Suzuki-Miyaura Coupling between 3-Iodolawsone and Arylboronic Acids. Synthesis of Lapachol Analogues with Antineoplastic and Antileishmanial Activities
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Suzuki-Miyaura Coupling between 3-Iodolawsone and Arylboronic Acids. Synthesis of Lapachol Analogues with Antineoplastic and Antileishmanial Activities

机译:3-碘代异黄酮和芳基硼酸之间的Suzuki-Miyaura偶联。具有抗肿瘤和抗利什曼活性的拉帕胆类似物的合成

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摘要

A series of 2-hydroxy-3-arylnaphthalene-1,4-diones (3-aryllawsones) were synthesized by Suzuki-Miyaura cross coupling reaction of 3-iodolawsone with arylboronic acids/esters. The hydroxylated resulting products were transformed into their corresponding N , N -diethyl carbamates. The antineoplastic and antileishmanial activities of the compounds were evaluated and compared with lapachol and its carbamate, providing promising results.
机译:通过3-碘代异黄酮与芳基硼酸/酯的Suzuki-Miyaura交叉偶联反应,合成了一系列2-羟基-3-芳基萘-1,4-二酮(3-芳基异丁烯)。将羟基化的所得产物转化为其相应的N,N-二乙基氨基甲酸酯。评估了该化合物的抗肿瘤和抗疟疾活性,并与拉帕酚及其氨基甲酸酯进行了比较,提供了可喜的结果。

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