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2022 , Vol. 42 >Issue 7: 2184 - 2191

DOI: https://doi.org/10.6023/cjoc202203011

研究论文

铑催化羧酸原位生成酰氟的脱羰Suzuki-Miyaura偶联

  • 刘晓洁 ,
  • 徐必平 ,
  • 苏伟平
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  • a福州大学化学学院 福建福州 350108
    b中国科学院福建物质结构研究所 结构化学国家重点实验室 福建福州 350002

收稿日期: 2022-03-03

  修回日期: 2022-04-02

  网络出版日期: 2022-04-11

基金资助

国家重点研发计划(2018FYA0704502); 国家自然科学基金(21931011); 国家自然科学基金(22071241); 中国福建光电信息科学与技术创新实验室(闽都创新实验室)(2021ZZ105)

收起

Rhodium-Catalyzed Decarbonylative Suzuki-Miyaura Cross-Coupling via in-Situ Generation of Acyl Fluorides from Carboxylic Acids

  • Xiaojie Liu ,
  • Biping Xu ,
  • Weiping Su
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  • aCollege of Chemistry, Fuzhou University, Fuzhou, Fujian 350108
    bState Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002
* E-mail: ;

Received date: 2022-03-03

  Revised date: 2022-04-02

  Online published: 2022-04-11

Supported by

National Key Research and Development Program of China(2018FYA0704502); National Natural Science Foundation of China(21931011); National Natural Science Foundation of China(22071241); Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China(2021ZZ105)

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摘要

联芳基类化合物是非常重要的有机结构, 并且它们广泛存在于药物、功能材料以及天然产物之中. 通过新颖而又独特的反应性, 脱羰反应绕过了脱羧反应, 在芳(杂环)羧酸必须有特定取代基的限制, 逐渐成为羧酸衍生物向联芳基类化合物转化合成中难以忽视的一类方法. 发展了一例铑催化羧酸原位生成酰氟的脱羰Suzuki-Miyaura偶联反应, 该方法对芳基羧酸和硼酸有很好的官能团兼容性, 甚至可以用来合成传统方法难以获得的天然产物和修饰药物.

关键词： 铑催化; 脱羰交叉偶联; 原位生成; 酰氟

本文引用格式

刘晓洁 , 徐必平 , 苏伟平 . 铑催化羧酸原位生成酰氟的脱羰Suzuki-Miyaura偶联[J]. 有机化学, 2022 , 42(7) : 2184 -2191 . DOI: 10.6023/cjoc202203011

Abstract

The biaryl frameworks are momentous organic backbones that are commonly occurred in pharmaceutical, functional materials and natural products. By virtue of the distinctive reactivity through state-of-the-art process, decarbonylative couplings, which have bypassed the restriction to specifically substituted (hetero)aryl carboxylic acids of decarboxylative couplings, gradually become unneglected methods in the conversion of carboxylic acid derivatives. Herein, a rhodium-catalyzed decarbonylative Suzuki-Miyaura cross-coupling via in-situ generation strategy of acyl fluorides from carboxylic acids was developed. This protocol shows eminent functional group tolerance with arrays of combinations between carboxylic acid and boronic acid. Furthermore, the reaction offers a new access to those conventionally unattainable biaryl motifs, including natural product and modified drugs.

Key words： rhodium catalysis; decarbonylative cross-coupling; in-situ generation; acyl fluorides

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