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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Diels-Alder cycloadditions of 3,5-dibromo-2-pyrone with cycloalkenyl silyl ethers for the synthesis of bicarbocycles
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Diels-Alder cycloadditions of 3,5-dibromo-2-pyrone with cycloalkenyl silyl ethers for the synthesis of bicarbocycles

机译:3,5-二溴-2-吡喃酮与环烯基甲硅烷基醚的Diels-Alder环加成反应合成二碳环

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摘要

3,5-Dibromo-2-pyrone underwent facile Diels-Alder [4+2] cycloadditions with cycloalkenyl silyl ethers to provide a series of tricyclolactones,with good to excellent chemical yields and stereoselectivity.The resulting cycloadducts could be readily converted into the corresponding bicarbocycles upon selective debromination and reductive lactone ring opening reactions.
机译:3,5-二溴-2-吡喃酮与环烯基甲硅烷基醚进行便捷的Diels-Alder [4 + 2]环加成反应,得到一系列三环内酯,具有良好的化学收率和立体选择性,所得环加合物可轻松转化为相应的环加合物选择性脱溴和还原性内酯开环反应生成二碳环。

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