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首页> 外文期刊>Bulletin of the Korean Chemical Society >Direct Palladium-Catalyzed C-4 Arylation of Tri-substituted Furans with Aryl Chlorides: An Efficient Access to Heteroaromatics
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Direct Palladium-Catalyzed C-4 Arylation of Tri-substituted Furans with Aryl Chlorides: An Efficient Access to Heteroaromatics

机译:三取代呋喃与芳基氯化物的直接钯催化C-4芳基化:高效获得杂芳烃

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摘要

A series of functionalized furans were synthesized by way of a palladium -catalyzed coupling reaction of 2,3,5- trisubstituted furans with aryl chlorides through C-H bond cleavages at C-4 position. The feature of the reaction was facilitative preparation of furan derivatives with good functional group tolerance. All reactions gave the desired products in moderate to good yields in the presences of BuAd2P and t-BuOK in DMF at 120 oC after 15 h.
机译:通过2,3,5-三取代的呋喃与芳基氯的钯催化偶联反应,通过C-4位的C-H键裂解,合成了一系列官能化的呋喃。该反应的特征是易于制备具有良好官能团耐受性的呋喃衍生物。在BuAd2P和t-BuOK在DMF中于15小时后于120 oC存在下,所有反应均以中等至良好的产率提供了所需的产物。

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