Rh(III)-Catalyzed Redox-neutral C-H Multifluoroalkenylation of Benzamides

Synthesis Pub Date : 2024-06-11 DOI:10.1055/a-2343-0676
Jia-Qiang Wu, Wei Lin, Yifei Qu, Mei Xie, Huixuan Zhu, Jinhui Hu, Zhuang Xiong, Jun Xu, Wenhua Chen
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Abstract

Fluorinated molecules are widely used in pharmaceutical and agrochemical industries. Multifluoroalkyl-containing compounds have attracted increasing attention for their unique ability to alter the activity of drugs and bioactive molecules. Herein, we report an efficient Rh(III)-catalyzed redox-neutral C-H multifluoroalkenylation of benzamides with multifluoroalkenes, which provides a versatile protocol for accessing a wide range of multifluoroalkenylated arenes.

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Rh(III)催化的苯甲酰胺氧化还原中性 C-H 多氟烯化反应
氟化分子广泛应用于制药和农用化学品行业。含多氟烷基的化合物因其改变药物和生物活性分子活性的独特能力而受到越来越多的关注。在此,我们报告了一种高效的 Rh(III) 催化的多氟烯烃与苯甲酰胺的氧化还原中性 C-H 多氟烯烃化反应,该反应为获得多种多氟烯烃化的炔类化合物提供了一种多功能方案。
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