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通过配体到金属的电荷转移实现的光催化氟烷基化反应。

Photocatalytic fluoroalkylation by ligand-to-metal charge transfer.

作者信息

Liu Jingyi, Cui Zhenwei, Bi Jingjing, He Xing, Ding Qingjie, Zhu Hong, Ma Chunhua

机构信息

Collaborative Innovation Centre of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Henan Engineering Research Centre of Chiral Hydroxyl Pharmaceutical, Henan Engineering Laboratory of Chemical Pharmaceutical and Biomedical Materials, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, China.

Chongqing Aoshe Bio-Chemical Co., Ltd., Chongqing, China.

出版信息

Front Chem. 2024 Sep 6;12:1481342. doi: 10.3389/fchem.2024.1481342. eCollection 2024.

DOI:10.3389/fchem.2024.1481342
PMID:39308850
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11412811/
Abstract

Trifluoromethyl (CF) and other fluoroalkyl groups are of great significance in the fields of pharmaceutical chemistry and agricultural chemicals. Fluoroalkyl acids, especially trifluoroacetic acid (TFA) is considered the most ideal fluoroalkylation reagent due to its low cost and easy availability. However, the extremely high oxidation potential requirement of TFA limits its wide application. In recent years, since visible-light-induced fluoroalkylation through the ligand-to-metal charge transfer (LMCT) process can overcome the above limitations, it has become an effective synthetic tool for the construction of fluorinated compounds with complex molecules and structures. In this review, according to the classification of different metal catalysts, we summarize the trifluoromethylation and fluoroalkylation of olefins, heteroaromatics, and terminal alkynes in different metal catalytic systems and their corresponding reaction mechanisms. The photocatalytic fluoroalkylation via LMCT is believed to expedite the development of fluoro-containing drugs, and more novel fluoroalkylation methologies using this strategy will be disclosed.

摘要

三氟甲基(CF)和其他氟烷基在药物化学和农药领域具有重要意义。氟烷基酸,尤其是三氟乙酸(TFA),因其成本低且易于获得,被认为是最理想的氟烷基化试剂。然而,TFA极高的氧化电位要求限制了其广泛应用。近年来,由于通过配体到金属电荷转移(LMCT)过程的可见光诱导氟烷基化能够克服上述限制,它已成为构建具有复杂分子和结构的氟化化合物的有效合成工具。在本综述中,根据不同金属催化剂的分类,我们总结了不同金属催化体系中烯烃、杂芳烃和末端炔烃的三氟甲基化和氟烷基化及其相应的反应机理。通过LMCT的光催化氟烷基化被认为将加速含氟药物的开发,并且将公开更多使用该策略的新型氟烷基化方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/04ab80216ce5/FCHEM_fchem-2024-1481342_wc_sch9.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/9b2fdb8122b5/FCHEM_fchem-2024-1481342_wc_sch5.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/9e5cc1e4e83f/FCHEM_fchem-2024-1481342_wc_sch7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/8bdf1a364929/FCHEM_fchem-2024-1481342_wc_sch8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/04ab80216ce5/FCHEM_fchem-2024-1481342_wc_sch9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/eaee4b3c2064/fchem-12-1481342-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/0b653f92aa68/FCHEM_fchem-2024-1481342_wc_sch1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/d0249e866d71/FCHEM_fchem-2024-1481342_wc_sch2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/b7643b3f1392/FCHEM_fchem-2024-1481342_wc_sch3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/d19cf54b7915/FCHEM_fchem-2024-1481342_wc_sch4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/9b2fdb8122b5/FCHEM_fchem-2024-1481342_wc_sch5.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7945/11412811/04ab80216ce5/FCHEM_fchem-2024-1481342_wc_sch9.jpg

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