首页> 外文期刊>Monatshefte fur Chemie >Combined palladium/eosin Y-catalysed direct synthesis of anticancer biarylquinolinooxazocino-quinoxaline-1-ones under visible light in one-pot sequence: a revisited proof of concept
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Combined palladium/eosin Y-catalysed direct synthesis of anticancer biarylquinolinooxazocino-quinoxaline-1-ones under visible light in one-pot sequence: a revisited proof of concept

机译:组合钯/ eosin Y催化的直接合成抗癌BiarallquinolinoOxazocino-喹喔啉-1- 1-罐子序列下可见光下的喹喔啉-1-酮:重新审议的概念证明

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摘要

A novel, efficient, and green catalytic system under visible light irradiation has been introduced for the synthesis of anticancer biarylquinolooxazocino-quinoxaline-1-ones in one-pot sequence. The developed synthetic approach will be successfully utilized for the synthesis of various bioactive biarylquinolone in near future. Also, the cytotoxicity profile of these scaffolds has unveiled their superb cytoselectivity in HeLa and MCF-7 cell line compared to cisplatin. Graphic abstract
机译:在可见光照射下的一种新颖,有效和绿色的催化系统,用于合成抗癌的Biarallquinolooxazocino-喹喔唑嗪-1-喹啉-1-酮。 开发的合成方法将成功地用于在不久的将来合成各种生物活性炭喹啉。 而且,与顺铂相比,这些支架的细胞毒性曲线在HelA和MCF-7细胞中揭开了它们的Sullb CytoSelectivity。 图形摘要

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