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A Benzoyl Peroxide/Diphenyl Diselenide Binary System for Functionalization of Alkynes Leading to Alkenyl and Alkynyl Selenides

机译:用于炔基和炔基硒化物的炔烃官能化的苯甲酰基/二苯基五烯酯二元体系

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摘要

Binary systems consisting of benzoyl peroxide (BPO) and diorganyl diselenide are effective in the selective benzoyloxyselenation of internal alkynes to afford the corresponding beta-(benzoyloxy)alkenyl selenides in good yields. In contrast to internal alkynes, terminal alkynes undergo a novel C(sp)-H substitution with the phenylseleno group of the BPO/(PhSe)(2) system, providing alkynyl selenides in good yields. Both selenation reactions might proceed via benzoyloxy selenide (PhC(O)O-SeAr) as a key intermediate for electrophilic addition to alkynes. The products alkenyl and alkynyl selenides are expected to be useful synthetic intermediates in organic synthesis.
机译:由苯甲酰基(BPO)和二氧化二元烯烃组成的二元系统在内部炔烃的选择性苯甲酰氧基化合物中是有效的,得到相应的β-(苯甲酰氧基)烯基硒化烷基。 与内部炔烃相反,终端炔烃与BPO /(PHSE)(2)系统的苯基硒基组进行了新的C(SP)-H取代,以良好的产率为炔基硒化酯提供。 硒化反应均可通过苯甲酰氧基硒(PHC(O)O-Sear)作为亲电离为炔烃的关键中间体。 产物链烯基和炔基硒化糖苷预期在有机合成中是有用的合成中间体。

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  • 来源
    《The Journal of Organic Chemistry》 |2017年第23期|共8页
  • 作者单位

    Osaka Prefecture Univ Grad Sch Engn Dept Appl Chem Naka Ku I-1 Gakuen Cho Sakai Osaka 5998531 Japan;

    Osaka Prefecture Univ Grad Sch Engn Dept Appl Chem Naka Ku I-1 Gakuen Cho Sakai Osaka 5998531 Japan;

    Osaka Prefecture Univ Grad Sch Engn Dept Appl Chem Naka Ku I-1 Gakuen Cho Sakai Osaka 5998531 Japan;

    Osaka Prefecture Univ Grad Sch Engn Dept Appl Chem Naka Ku I-1 Gakuen Cho Sakai Osaka 5998531 Japan;

    Saga Univ Ctr Educ &

    Res Agr Innovat Fac Agr 152-1 Shonan Cho Karatsu Saga 8470021 Japan;

    Osaka Prefecture Univ Grad Sch Life &

    Environm Sci Dept Appl Biosci Naka Ku 1-1 Gakuen Cho Sakai Osaka 5998531 Japan;

    Osaka Prefecture Univ Grad Sch Engn Dept Appl Chem Naka Ku I-1 Gakuen Cho Sakai Osaka 5998531 Japan;

    Osaka Prefecture Univ Grad Sch Engn Dept Appl Chem Naka Ku I-1 Gakuen Cho Sakai Osaka 5998531 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
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