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首页> 外文期刊>Chemical Communications >A fast and selective decarboxylative difunctionalization and cyclization for easy access to gem-dihalo alcohol, ether, ester and bromo-1,4-dioxane
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A fast and selective decarboxylative difunctionalization and cyclization for easy access to gem-dihalo alcohol, ether, ester and bromo-1,4-dioxane

机译:快速且选择性的脱羧双官能化和环化,可轻松获得宝石二卤代醇,醚,酯和溴代1,4-二恶烷

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摘要

A general strategy for fast decarboxylative difunctionalization to gem-dihalohydrin, gem-dihaloether, gem-dibromoester and cyclized bromo-l,4-dioxane synthons with outstanding regio-and stereoselectivity is demonstrated.
机译:证明了快速脱羧双官能化为宝石-二卤代醇,宝石-二卤代醚,宝石-二溴酸酯和环化的溴-1,4-二恶烷合成子的一般策略,该区域具有出色的区域选择性和立体选择性。

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  • 来源
    《Chemical Communications 》 |2011年第47期| p.12667-12669| 共3页
  • 作者单位

    Department of Chemistry, University of Calcutta,University College of Science, 92, A.P.C. Road, Kolkata-700009,India;

    Department of Chemistry, University of Calcutta,University College of Science, 92, A.P.C. Road, Kolkata-700009,India;

    Department of Chemistry, University of Calcutta,University College of Science, 92, A.P.C. Road, Kolkata-700009,India;

    Department of Chemistry, University of Calcutta,University College of Science, 92, A.P.C. Road, Kolkata-700009,India;

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