首页> 外文期刊>The Journal of Organic Chemistry >N-Iodosuccinimide-Initiated Spirocyclopropanation of Styrenes with 1,3-Dicarbonyl Compound for the Synthesis of Spirocyclopropanes
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N-Iodosuccinimide-Initiated Spirocyclopropanation of Styrenes with 1,3-Dicarbonyl Compound for the Synthesis of Spirocyclopropanes

机译:N-碘代琥珀酰亚胺引发的苯乙烯与1,3-二羰基化合物的螺环丙烷化反应,用于合成螺环丙烷

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摘要

Herein is reported an N-iodosuccinimide-initiated spirocyclopropanation reaction of styrenes with 1,3-dicarbonyl compounds in the presence of white LED light. The reaction proceeds via two C-H and two C-I bond cleavage event, along with two C-C bond formation event, and formation of quaternary centers. These reactions could be carried out at room temperature and tolerated a wide range of substrates, resulting in good to excellent chemical yields. This developed radical reaction provides easy and practical access to spiro[2.4]heptane-4,7-dione derivatives.
机译:本文报道了在白色LED光的存在下苯乙烯与1,3-二羰基化合物的N-碘代琥珀酰亚胺引发的螺环丙烷化反应。该反应通过两个C-H和两个C-I键裂解事件,两个C-C键形成事件以及季中心的形成而进行。这些反应可以在室温下进行,并能耐受多种底物,从而获得良好的化学收率。这种发达的自由基反应提供了简便实用的螺[2.4]庚烷-4,7-二酮衍生物。

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