Microwave-assisted, [Bmim]HSO4-catalyzed the Friedländer quinoline synthesis of quinoline under solvent-free conditions

IF 0.9 Q4 CHEMISTRY, PHYSICAL

Current Organocatalysis Pub Date : 2022-01-27 DOI:10.2174/2213337209666220127142333

D. Duc, V. C. Dung

引用次数: 0

Abstract

An efficient and green method for the Friedländer quinoline synthesis is described. The synthesis was performed under microwave irradiation using ionic liquid [Bmim]HSO4 as a catalyst. A diverse range of quinoline derivatives was obtained in high yields from 2‐aminoaryl aldehydes and ketones under solvent-free conditions.

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微波辅助下，[Bmim] hso4在无溶剂条件下催化Friedländer喹啉合成

介绍了一种高效、绿色的Friedländer喹啉合成方法。使用离子液体[Bmim]HSO4作为催化剂在微波辐射下进行合成。在无溶剂条件下，2-氨基芳基醛和酮以高产率获得了各种喹啉衍生物。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Current Organocatalysis CHEMISTRY, PHYSICAL-

CiteScore

2.00

自引率

0.00%

发文量

期刊介绍： Current Organocatalysis is an international peer-reviewed journal that publishes significant research in all areas of organocatalysis. The journal covers organo homogeneous/heterogeneous catalysis, innovative mechanistic studies and kinetics of organocatalytic processes focusing on practical, theoretical and computational aspects. It also includes potential applications of organocatalysts in the fields of drug discovery, synthesis of novel molecules, synthetic method development, green chemistry and chemoenzymatic reactions. This journal also accepts papers on methods, reagents, and mechanism of a synthetic process and technology pertaining to chemistry. Moreover, this journal features full-length/mini review articles within organocatalysis and synthetic chemistry. It is the premier source of organocatalysis and synthetic methods related information for chemists, biologists and engineers pursuing research in industry and academia.