首页> 外文期刊>The Journal of Organic Chemistry >Microwave-assisted one-pot synthesis of isoquinolines, furopyridines, and thienopyridines by palladium-catalyzed sequential coupling-imination-annulation of 2-bromoarylaldehydes with terminal acetylenes and ammonium acetate
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Microwave-assisted one-pot synthesis of isoquinolines, furopyridines, and thienopyridines by palladium-catalyzed sequential coupling-imination-annulation of 2-bromoarylaldehydes with terminal acetylenes and ammonium acetate

机译:钯辅助2-溴芳醛与末端乙炔和乙酸铵的钯催化连续偶合-环化-微波辅助一锅合成异喹啉,呋喃吡啶和噻吩吡啶

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摘要

A palladium-catalyzed microwave-assisted one-pot reaction for the synthesis of isoquinolines is developed. The reaction is carried out by sequential coupling-imination-annulation reactions of ortho-bromoarylaldehydes and terminal alkynes with ammonium acetate, and a variety of substituted isoquinolines, furopyridines, and thienopyridines is prepared in moderate to excellent yields (up to 86%).
机译:开发了钯催化的微波辅助一锅法合成异喹啉。该反应通过邻溴芳基醛和末端炔烃与乙酸铵的顺序偶合-胺化-环化反应进行,制备了各种取代的异喹啉,呋喃吡啶和噻吩并吡啶,产率中等至优异(最高86%)。

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