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Enantioselective Nickel-Catalyzed anti-Carbometallative Cyclizations of Alkynyl Electrophiles Enabled by Reversible Alkenylnickel E/Z Isomerization

机译:可逆的烯基镍E / Z异构化对炔基亲电子的对映选择性镍催化的抗碳金属环化

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摘要

Nickel-catalyzed additions of arylboronic acids to alkynes, followed by enantioselective cyclizations of the alkenylnickel species onto tethered ketones or enones, are reported. These reactions are reliant upon the formal anti-carbonickelation of the alkyne, which is postulated to occur by the reversible E/Z isomerization of an alkenylnickel species.
机译:据报道,镍催化将芳基硼酸加成到炔烃上,然后烯基镍物种对映选择性环化到束缚的酮或烯酮上。这些反应依赖于炔烃的形式上的抗羰基化,推测是通过链烯基镍物种的可逆E / Z异构化发生的。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2016年第26期|8068-8071|共4页
  • 作者单位

    School of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, United Kingdom;

    School of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, United Kingdom;

    School of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, United Kingdom;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:08:50

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