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Cobalt-Catalyzed Allylic C(sp~3)-H Carboxylation with CO_2

机译:钴催化的CO_2烯丙基C(sp〜3)-H羧化反应

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摘要

Catalytic carboxylation of the allylic C-(sp~3)-H bond of terminal alkenes with CO_2 was developed with the aid of a Co/Xantphos complex. A wide range of allylarenes and 1,4-dienes were successfully transformed into the linear styrylacetic acid and hexa-3,5-dienoic acid derivatives in moderate to high yields, with excellent regioselectivity. The carboxylation showed remarkable functional group tolerability, so that selective addition to CO_2 occurred in the presence of other carbonyl groups such as amide, ester, and ketone. Since styrylacetic acid derivatives can be readily converted into optically active γ-butyrolactones through Sharpless asymmetric dihydroxylation, this allylic C(sp~3)-H carboxylation showcases a facile synthesis of γ-butyrolactones from simple allylarenes via short steps.
机译:借助Co / Xantphos配合物开发了末端烯烃与CO_2的烯丙基C-(sp〜3)-H键的催化羧化反应。多种烯丙基芳烃和1,4-二烯成功地以中等至高收率成功转化为线性苯乙烯基乙酸和六-3,5-二烯酸衍生物,并具有出色的区域选择性。羧化反应显示出显着的官能团耐受性,因此在存在其他羰基(例如酰胺,酯和酮)的情况下,选择性地向CO_2加成。由于苯乙烯基乙酸衍生物可通过Sharpless不对称二羟基化反应轻松转化为旋光性γ-丁内酯,因此该烯丙基C(sp〜3)-H羧化反应显示了从简单的烯丙基芳烃通过短步合成γ-丁内酯的简便方法。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2017年第17期|6094-6097|共4页
  • 作者单位

    Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan;

    Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan;

    Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan;

  • 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 03:07:57

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