首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >Synthesis of racemic and optically active forms of novel antimalarial agents, spirocyclopentanone-anthracene adducts, via tandem Michael addition-Dieckmann condensation reactions as the key steps
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Synthesis of racemic and optically active forms of novel antimalarial agents, spirocyclopentanone-anthracene adducts, via tandem Michael addition-Dieckmann condensation reactions as the key steps

机译:通过串联迈克尔加成-狄克曼缩合反应合成新型抗疟药消旋和旋光形式的螺环戊酮-蒽加合物

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摘要

Spirocyclopentanone-anthracene adducts, novel antimalarial agents, have been synthesized by employing the racemic and the optically active dimethyl itaconate-anthracene adducts in a reaction with piperine via tandem Michael addition-Dieckmann condensation reactions as the key steps. All adducts exhibited antimalarial activity with IC _(50) values of 3.4-4.7 μg/mL, and importantly displayed non-cytotoxicity to vero cells.
机译:通过将外消旋和旋光性衣康酸二甲基衣康酸酯-蒽加合物与胡椒碱反应,通过串联迈克尔加成-狄克曼缩合反应,合成了螺环戊酮-蒽加合物(新型抗疟药)。所有加合物均表现出抗疟活性,IC _(50)值为3.4-4.7μg/ mL,并且重要地显示出对Vero细胞无细胞毒性。

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