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首页> 外文期刊>Organic & biomolecular chemistry >Bu_4NI-catalyzed, oxidative C_((SP~2))-C_((SP~3)) cross dehy-drogenative coupling for the regioselective direct C-3 benzylation of 2H-indazoles
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Bu_4NI-catalyzed, oxidative C_((SP~2))-C_((SP~3)) cross dehy-drogenative coupling for the regioselective direct C-3 benzylation of 2H-indazoles

机译:Bu_4ni催化,氧化C _((SP〜2)) - C _((SP〜3))对2H- Indazoles的区域选择性直接C-3苄基化的交叉凋亡偶联

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摘要

A Bu_4NI-catalyzed, DTBP-promoted, regioselective C_((SP~2))-C_((SP~3)) cross dehydrogenative coupling (CDC) protocol for the direct C-3 benzylation of 2H-indazoles is reported. The metal-free protocol is operationally simple and proceeds mechanistically via the generation of stable benzylic free-radicals followed by regioselective addition at the C-3 position of 2H-indazoles which afforded C-3 benzylated 2H-indazoles up to 87% yields. The methodology showed a varied array of functional group tolerance and wide substrate compatibility. The gram-scale synthesis further highlights the importance and versatile nature of this methodology.
机译:据报道,Bu_4NI催化的DTBP促进的促进区域选择性C _((SP〜2)) - C _((SP〜3))交叉脱氢偶联(CDC)方案用于2H-吲唑的直接C-3苄基化。无金属的方案在操作上简单,通过产生稳定的苄基自由基,然后在2H-吲唑的C-3位置的稳定性添加,得到C-3苄基化的2H-吲唑,得到高达87%的产率。该方法显示了各种功能基团耐受性和宽基板兼容性。革兰尺合成进一步突出了该方法的重要性和多功能性质。

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  • 来源
    《Organic & biomolecular chemistry》 |2020年第30期|5927-5936|共10页
  • 作者

    Lalit Yadav; Sandeep Chaudhary;

  • 作者单位

    Laboratory of Organic and Medicinal Chemistry (OMC Lab) Department of Chemistry Malaviya National Institute of Technology Jawaharlal Nehru Marg Jaipur 302017 India;

    Laboratory of Organic and Medicinal Chemistry (OMC Lab) Department of Chemistry Malaviya National Institute of Technology Jawaharlal Nehru Marg Jaipur 302017 India;

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