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Cu(II)-Promoted Transformations of 伪-Thienylcarbinols into Spirothienooxindoles: Regioselective Halogenation of Dienyl Sulfethers Containing Electron-Rich Aryl Rings
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文摘
Under the promotion of Cu(II) salts, the 伪-thienylcarbinols with an N-phenyl carbonyl group at the other 伪-position are converted into three different ranges of spirothienooxindoles involving dearomatizing Friedel鈥揅rafts reaction. In addition, the unprecedented regioselective CuX2-mediated C鈥揌 functionalization/halogenation of dienyl sulfether containing electron-rich aryl rings is presented.

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