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Asymmetric Dearomatization of Naphthols via a Rh-Catalyzed C(sp~2)-H Functionalization/Annulation Reaction

机译:通过Rh催化的C(sp〜2)-H官能化/环合反应使萘酚不对称脱芳香化

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摘要

A Rh-catalyzed enantioselective dearomatization of 1-aryl-2-naphthols with internal alkynes via C-H functionalization reaction was achieved. In the presence of a chiral Cp/Rh catalyst and combined oxidants of Cu(OAc)_2 and air (oxygen), various highly enantioen-riched spirocyclic enones bearing an all-carbon quaternary stereogenic center could be synthesized in 33-98% yields with up to 97:3 er.
机译:通过C-H官能化反应,实现了Rh催化的1-芳基-2-萘酚与内部炔烃的对映体选择性脱芳香化反应。在手性Cp / Rh催化剂和Cu(OAc)_2与空气(氧气)混合氧化剂的存在下,可以合成具有全碳季立体中心的各种高度对映体富集的螺环烯酮,收率为33-98%。高达97:3 er。

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  • 来源
    《Journal of the American Chemical Society》 |2015年第15期|4880-4883|共4页
  • 作者单位

    State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China;

    State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China;

    State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China;

    State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:09:38

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