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Carbolithiation of meso-aryl-substituted 5,15-diazaporphyrin selectively provides 3-alkylated diazachlorins

机译:介孔芳基取代的5,15-二氮杂卟啉的羰基化选择性地提供3-烷基化的二氮杂绿素

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摘要

Treatment of meso-mesityl 5,15-diazaporphyrin with alkyllithiums in toluene at low temperature provided monoalkylated diazachlorins through highly regioselective nucleophilic addition at the β-position near the meso-nitrogen atom.
机译:在低温下用烷基锂在甲苯中处理间苯二甲酰基5,15-二氮杂卟啉,通过在中氮原子附近的β位上进行高度区域选择性的亲核加成反应,提供了单烷基化的二氮杂ins呤。

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  • 来源
    《Chemical Communications》 |2013年第44期|5064-5066|共3页
  • 作者单位

    Department of Applied Chemistry, Grqduate School of Engineering, Nagoya University, Chikusa-ku, Nagoya 464-8603, Japan;

    Department of Applied Chemistry, Grqduate School of Engineering, Nagoya University, Chikusa-ku, Nagoya 464-8603, Japan;

    Department of Applied Chemistry, Grqduate School of Engineering, Nagoya University, Chikusa-ku, Nagoya 464-8603, Japan;

    Department of Applied Chemistry, Grqduate School of Engineering, Nagoya University, Chikusa-ku, Nagoya 464-8603, Japan;

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  • 入库时间 2022-08-17 13:18:23

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