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Palladium-Catalyzed Carbonylative Cyclization of Aryl Alkenes/Alkenols: A New Reaction Mode for the Synthesis of Electron-Rich Chromanes

机译:钯催化的芳烃/烯烃的羰基化环化:合成电子丰富的色氨酸的新反应模式

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摘要

The Pd(II)-catalyzed intramolecular carbonylative cyclization reaction of aryl alkenes and aryl alkenols is reported for the synthesis of structurally diverse chromanes. PdCl2(CH3CN)(2) was used as the catalyst and CuCl2 as the oxidant under the balloon pressure of CO. The reaction is conducted under mild conditions, and chromane-type esters and lactones can be generated in a highly regio- and stereoselective manner.
机译:据报道,Pd(II)催化的芳基烯烃和芳基烯醇的分子内羰基化环化反应可合成结构多样的苯并二氢吡喃。在CO的球囊压力下,使用PdCl2(CH3CN)(2)作为催化剂,使用CuCl2作为氧化剂。反应在温和的条件下进行,并且可以以高度区域和立体选择性的方式生成苯并吡喃型酯和内酯。

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