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Synthesis of 2,3-dihydrofurans via Lewis acid-Catalyzed [4+1] Cycloaddition of Enynones with Sulfoxonium Ylides in Ionic Liquids: A Mild and Green Platform

机译:通过刘易斯酸催化的[4+1]在离子液体中用磺氧酮的Enynone的烯酮合成2,3-二氢呋喃[4+1]

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摘要

The zinc-catalyzed [4+1] cycloadddition followed by intramolecular insertion reaction between enynones and sulfoxonium ylides for the synthesis of multisubstituted 2,3-dihydrofurans in ionic liquids is described.This highly efficient and stepeconomical reaction displays excellent functional group compatibility and stereoselectivity.The reaction media colud maintain high reaction activity even after six cycles.
机译:锌催化的[4+1]环载体,然后在离子液体中的多取代的2,3-二氢呋喃的合成中,描述了高效和步骤反应的多功能2,3-二氢呋喃。 反应培养基即使在六个周期后仍保持高反应活性。

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