Electro-photochemical Functionalization of C(sp3)–H bonds: Synthesis toward Sustainability

JACS Au Pub Date : 2024-09-09 DOI:10.1021/jacsau.4c00496
Puja Singh, Burkhard König, Aslam C. Shaikh
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Abstract

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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C(sp3)-H 键的电光化学功能化:面向可持续性的合成
在过去几十年中,由于 C(sp3)-H 键在各个领域的应用前景广阔,人们对利用其功能化的兴趣急剧上升。然而,传统方法在很大程度上依赖于一定量的昂贵且通常对环境有害的金属氧化剂,给整个 C-H 活化化学带来了可持续发展的挑战。与此形成鲜明对比的是,电光催化驱动的 C(sp3)-H 键活化技术的出现提供了一种变革性的替代方法。这种方法为碳-碳和碳-杂原子键的形成提供了一条可行的途径。它无需预官能化或苛刻的反应条件,直接与有机化合物中普遍存在的惰性 C(sp3)-H 键结合,从而脱颖而出。这种方法简化了复杂有机化合物的合成,有助于高效、精确地创建新型化学结构。本综述旨在阐明近年来在通过有机电光化学实现 C(sp3)-H 键官能化领域取得的显著进展。
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