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首页> 外文期刊>Tetrahedron >A novel construction of quino-fused tropone skeleton: first synthesis of 12H-benzo[4,5]cyclohepta[1,2-b]quinolin-12-one derivatives
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A novel construction of quino-fused tropone skeleton: first synthesis of 12H-benzo[4,5]cyclohepta[1,2-b]quinolin-12-one derivatives

机译:一种新型的喹诺酮的托酮骨架的构建:12H-苯并[4,5]环庚[1,2-b]喹啉-12-一衍生物的首次合成

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摘要

In the present investigation, the incorporation of both quinoline moiety and tropone ring in a molecule frame work in fused form leading to a series of structurally novel and biologically intriguing quinoline/ tropone hybrids 12H-benzo[4,5]cyclohepta[1,2-b]quinolin-12-one derivatives has been first achieved through a simple, and economical two-step procedure, involving the one-pot synthesis of (E)-2-(arylvinyl) quinoline-3-carboxylic acids followed by intramolecular FriedeleCrafts acylation reaction using polyphosphoric acid (PPA).
机译:在本研究中,喹啉部分和托环酮环在分子框架中的融合以融合形式起作用,从而导致一系列结构新颖且生物学上令人着迷的喹啉/托洛酮杂化物12H-苯并[4,5]环庚[1,2- b] quinolin-12-one衍生物已首先通过简单,经济的两步程序获得,涉及一锅合成(E)-2-(芳基乙烯基)喹啉3-羧酸,然后进行分子内FriedeleCrafts酰化使用多磷酸(PPA)进行反应。

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