表面改性
持续性
化学
光化学
生态学
物理化学
生物
作者
Puja Singh,Burkhard König,Aslam C. Shaikh
出处
期刊:JACS Au
[American Chemical Society]
日期:2024-09-09
卷期号:4 (9): 3340-3357
被引量:20
标识
DOI:10.1021/jacsau.4c00496
摘要
Over the past several decades, there has been a surge of interest in harnessing the functionalization of C(sp3)-H bonds due to their promising applications across various domains. Yet, traditional methodologies have heavily leaned on stoichiometric quantities of costly and often environmentally harmful metal oxidants, posing sustainability challenges for C-H activation chemistry at large. In stark contrast, the emergence of electro-photocatalytic-driven C(sp3)-H bond activation presents a transformative alternative. This approach offers a viable route for forging carbon-carbon and carbon-heteroatom bonds. It stands out by directly engaging inert C(sp3)-H bonds, prevalent in organic compounds, without the necessity for prefunctionalization or harsh reaction conditions. Such methodology simplifies the synthesis of intricate organic compounds and facilitates the creation of novel chemical architectures with remarkable efficiency and precision. This review aims to shed light on the notable strides achieved in recent years in the realm of C(sp3)-H bond functionalization through organic electro-photochemistry.
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