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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >DABCO-catalyzed one-pot three component synthesis of dihydropyrano[3,2-c]chromene substituted quinazolines and their evaluation towards anticancer activity
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DABCO-catalyzed one-pot three component synthesis of dihydropyrano[3,2-c]chromene substituted quinazolines and their evaluation towards anticancer activity

机译:DABCO催化二氢吡喃并[3,2-c]色烯取代的喹唑啉的一锅三组分合成及其对抗癌活性的评价

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摘要

A facile DABCO promoted one-pot three component synthesis of a new series of C-C linked bis-hetero-cycle containing dihydropyrano[c]chromene as highly fused oxa-heteryl group at C-2 position of quinazoline was developed. Quinazoline-2-carbaldehyde, substituted 4-hydroxycoumarin and ethyl cyanoacetate were used as key components in the Knoevenagel-Michael addition reaction to get the titled compounds. These compounds were screened for anti-cancer activity against the breast cancer cell lines of MDA-MB 231, and MDA-MB 453. (C) 2016 Elsevier Ltd. All rights reserved.
机译:开发了一种简便的DABCO促进了一系列新的一系列C-C连接的双杂环的单组分三组分合成,该双杂环包含二氢吡喃并[c]苯甲基作为喹唑啉C-2位的高度稠合的氧杂杂基。喹唑啉-2-甲醛,取代的4-羟基香豆素和氰基乙酸乙酯用作Knoevenagel-Michael加成反应的关键组分,得到标题化合物。筛选了这些化合物对MDA-MB 231和MDA-MB 453乳腺癌细胞系的抗癌活性。(C)2016 Elsevier Ltd.保留所有权利。

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