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Solvent-Free Synthesis and In Vitro Antitumor Activity of a New Class of (Z)-3-Arylidene-1H-pyrano[3,4-b]quinolin- 4(3H)-ones

机译:新的(z)-3-芳基二苯甲酸[3,4-b] quinolin- 4(3H)-Ones的新类别(Z)-3-芳基二苯甲酸的新类别的无溶剂合成和体外抗肿瘤活性

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摘要

In the present investigation, an efficient and green synthesis of an intriguing array of structurally novel quinoline-based α- arylidene cycloketones i. e., (Z)-3-arylidene/ferrocenylmeth- ylene-5-methyl/phenyl-1H-pyrano[3,4-b]quinolin-4(3H)-ones (6a-z, 6aa and 6ab) has been successfully accomplished involving solvent-free reaction between pyrano[3,4-b]quinolin- 4(3H)-ones (7a-b) and various aromatic aldehydes by simple hand-grinding in a mortar and pestle using KOH as base at room temperature. The synthetic strategy has the attractive features such as experimental simplicity, mild and environ- mentally benign reaction conditions, easy work-up procedure and good yields.
机译:在本研究中,有效而绿色的合成是一系列有趣的结构新型喹啉基α-芳基芳基环酮i。 e。,(z)-3-芳基/亚利苯基 - Ylene-5-甲基/苯基/苯基-1H-Pyrano [3,4-B] quinolin-4(3H)-ONES(6A-Z,6AA和6AA) 成功完成了涉及pyrano [3,4-B]喹啉-4(3H)-ONS(7A-B)和各种芳族醛之间的无溶剂反应,通过在室温下使用KOH作为基础在砂浆中简单地手工磨碎的各种芳族醛。 。 合成策略具有吸引人的特征,例如实验性简单,轻度和环境良性反应条件,易于锻炼程序和良好的收率。

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