首页> 外文期刊>Medicinal chemistry >Regioselective Synthesis of 2-Chloroquinoline Based Ethyl 4-(3-Hydroxyphenyl)-2,7,7-Trimethyl-5-Oxo-1,4,5,6,7,8-Hexahydroquinoline-3-Carboxylates and their In-Silico Evaluation Against P-falciparum Lactate Dehydrogenase
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Regioselective Synthesis of 2-Chloroquinoline Based Ethyl 4-(3-Hydroxyphenyl)-2,7,7-Trimethyl-5-Oxo-1,4,5,6,7,8-Hexahydroquinoline-3-Carboxylates and their In-Silico Evaluation Against P-falciparum Lactate Dehydrogenase

机译:基于2-氯喹啉的乙基4-(3-羟基苯基)-2,7,7-三甲基-5-氧-1,4,5,6,7,8-六氢喹啉-3-羧酸的区域选择性合成及其硅内对恶性疟原虫乳酸脱氢酶的评价

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摘要

The reaction of various substituted 2, 4-dichloroquinolines with ethyl 4-(3-hydroxyphenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate was carried out in the presence of K2CO3 as a mild and efficient base at controlled temperature leading to novel 2-chloroquinoline based polyhydroquinoline with high regioselectivity. All the synthesized compounds were characterized using IR, NMR, Mass spectral data and then subjected to an in-silico analysis against P. falciparum lactate dehydrogenase.
机译:各种取代的2,4-二氯喹啉与4-(3-羟苯基)-2,7,7-三甲基-5-氧代-1,4,5,6,7,8-六氢喹啉-3-羧酸乙酯的反应为在温和有效的碱K2CO3存在下,在受控温度下进行,得到了具有高区域选择性的新型2-氯喹啉基聚氢喹啉。使用IR,NMR,质谱数据对所有合成的化合物进行表征,然后针对恶性疟原虫乳酸脱氢酶进行计算机模拟分析。

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