New Opportunities to Access Fluorinated Molecules Using Organophotoredox Catalysis via C(sp3)-F Bond Cleavage.

IF 8.7 Q1 CHEMISTRY, MULTIDISCIPLINARY JACS Au Pub Date : 2025-02-07 eCollection Date: 2025-02-24 DOI:10.1021/jacsau.4c01158
Sourav Roy, Tatiana Besset
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Abstract

Fluorinated molecules are of paramount importance because of their unique properties. As a result, the search for innovative approaches to the synthesis of this class of compounds has been relentless over the years. Among these, the combination of photocatalysis and organofluorine chemistry turned out to be an effective partnership to access unattainable fluorinated molecules. This Perspective provides an overview of the recent advances in synthesizing fluorinated molecules via an organophotoredox-catalyzed defluorination process from trifluoromethylated compounds. It encompasses the preparation of difluoromethylated (hetero)arenes, amides, and esters as well as gem-difluoroalkene derivatives using C(sp3)-F bond activation or β-fragmentation. This Perspective will highlight remaining challenges and discuss future research opportunities.

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通过 C(sp3)-F 键裂解利用有机光氧催化获得含氟分子的新机会。
氟化分子因其独特的性质而具有极其重要的意义。因此,多年来,对这类化合物合成的创新方法的探索一直是无情的。其中,光催化与有机氟化学的结合是获得难以获得的氟化分子的有效伙伴关系。本展望概述了通过有机光氧化还原催化三氟甲基化化合物脱氟工艺合成氟化分子的最新进展。它包括制备二氟甲基化(杂)芳烃,酰胺和酯,以及宝石-二氟烯烃衍生物使用C(sp3)-F键激活或β-裂解。这篇展望文章将强调仍然存在的挑战,并讨论未来的研究机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
9.10
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0.00%
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审稿时长
10 weeks
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