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Iron-catalyzed regio- and stereoselective addition of acid chlorides to alkynes

机译:铁催化的酰基氯向炔烃的区域和立体选择性加成

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摘要

An iron-catalyzed regio- and stereoselective addition of acid chlorides to alkynes has been described. The reaction utilizes an inexpensive iron catalyst system and it is suitable for the formation of a variety of bifunctional molecules. This is an inexpensive, regio-, stereoselective and atom-economical approach to β-chloro-α,β-unsaturated ketones from simple and readily available starting materials.
机译:已经描述了铁催化的酰基氯向炔的区域和立体选择性加成。该反应利用廉价的铁催化剂体系,并且适合于形成多种双功能分子。这是一种从简单易得的起始原料制得β-氯-α,β-不饱和酮的廉价,区域,立体选择性和原子经济的方法。

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  • 来源
    《Chemical Communications》 |2010年第32期|P.5891-5893|共3页
  • 作者单位

    Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China;

    Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China;

    Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China;

    Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000, P. R. China State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, P. R. China;

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  • 入库时间 2022-08-17 13:24:11

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