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Transition-Metal-Free Formylation of Allylzinc Reagents Leading to α-Quaternary Aldehydes

机译:烯丙基锌试剂的无金属无金属甲醛,导致α-季醛醛

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摘要

The first example of formylation of allylzinc reagents using S -phenyl thioformate is presented. The reaction proceeded under mild conditions without any transition-metal catalyst, forming quaternary carbon centers with reactive functionalities, such as formyl and vinyl groups. Moreover, Barbier-type formylation of an allylic bromide with a sterically demanding thioformate was achieved. As a preliminary result, asymmetric formylation was conducted using a menthol-derived chiral thioformate.
机译:介绍了使用S-苯基硫代甲酸酯的烯丙锌试剂的甲酰化的第一实例。 反应在不含任何过渡金属催化剂的温和条件下进行,形成具有反应性官能团的季碳中心,例如甲酰基和乙烯基。 此外,达到了甘蓝溴化物的倒胆型溴化物,其具有空间急需硫甲酰胺。 作为初步结果,使用薄荷醇衍生的手性硫甲酸酯进行不对称甲型化。

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  • 来源
    《Organic letters》 |2018年第6期|共4页
  • 作者单位

    Department of Applied Chemistry Institute of Science and Engineering Chuo University 1-13-27 Kasuga Bunkyo-ku Tokyo 112-8551 Japan;

    Department of Applied Chemistry Institute of Science and Engineering Chuo University 1-13-27 Kasuga Bunkyo-ku Tokyo 112-8551 Japan;

    Department of Applied Chemistry Institute of Science and Engineering Chuo University 1-13-27 Kasuga Bunkyo-ku Tokyo 112-8551 Japan;

    Department of Applied Chemistry Institute of Science and Engineering Chuo University 1-13-27 Kasuga Bunkyo-ku Tokyo 112-8551 Japan;

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  • 正文语种 eng
  • 中图分类 有机化学;
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