首页> 外文期刊>The Journal of Organic Chemistry >Intramolecular cycloaddition reactions of cis -1,2-dihydrocatechol derivatives incorporating C3-tethered diazoketones, nitrile oxides, and azides: Stereocontrolled routes to enantiomerically pure spiro[5.5]undecanes and related systems
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Intramolecular cycloaddition reactions of cis -1,2-dihydrocatechol derivatives incorporating C3-tethered diazoketones, nitrile oxides, and azides: Stereocontrolled routes to enantiomerically pure spiro[5.5]undecanes and related systems

机译:顺式-1,2-二氢邻苯二酚衍生物的分子内环加成反应,并结合有C3系的重氮酮,腈氧化物和叠氮化物:立体控制的对映体纯螺[5.5]十一烷和相关体系的途径

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摘要

A series of enantiomerically pure cis-1,2-dihydrocatechol derivatives incorporating C3-tethered diazoketone, nitrile oxide, or azide residues has been prepared from the precursor iodide 7 using Negishi cross-coupling reactions. Such derivatives, including diazoketone 12, participate in regio- and stereo-selective intramolecular cycloaddition reactions to give adducts, for example, 15, that are readily elaborated to spiro[5.5]undecanes such as 18.
机译:使用Negishi交叉偶联反应,从前体碘化物7制备了一系列对映体纯的顺式1,2-二氢邻苯二酚衍生物,其中并入有C3链状的重氮酮,氧化腈或叠氮化物残基。此类衍生物(包括重氮酮12)参与区域和立体选择性分子内环加成反应,生成加合物(例如15),这些加合物很容易合成成螺[5.5]十一烷(例如18)。

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