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首页> 外文期刊>Catalysis Communications >Simple, efficient copper-free Sonogashira coupling of haloaryl carboxylic acids or unactivated aryl bromides with terminal alkynes
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Simple, efficient copper-free Sonogashira coupling of haloaryl carboxylic acids or unactivated aryl bromides with terminal alkynes

机译:卤代芳基羧酸或未活化的芳基溴化物与末端炔烃的简单有效的无铜Sonogashira偶联

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摘要

In the absence of Cu(I), the catalytic coupling of haloaryl carboxylic acids or unactivated aryl bromides with terminal alkynes are shown to occur in the presence of 10equiv. piperidine at 85 °C within 20 min using PdCl2(PPh3)2 as catalyst in good to excellent yields. This procedure avoids the carboxy group protection/deprotection steps and enhances the total yield to simplify the synthesis of acetylenic retinoids. It is noteworthy that this protocol employs direct, mild and efficient copper-free reaction conditions.
机译:在不存在Cu(I)的情况下,卤代芳基羧酸或未活化的芳基溴化物与末端炔烃的催化偶联显示在存在10equiv的情况下发生。使用PdCl2(PPh3)2作为催化剂,在85°C下20分钟内可得到哌啶,收率良好。该程序避免了羧基的保护/去保护步骤,并提高了总产率以简化炔类视黄醇的合成。值得注意的是,该方案采用直接,温和和有效的无铜反应条件。

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