Sheikhaleslami Sahra, Sperry Jonathan
Centre for Green Chemical Science, School of Chemical Sciences, University of Auckland, New Zealand.
Chemistry. 2025 Jan 2;31(1):e202403833. doi: 10.1002/chem.202403833. Epub 2024 Nov 18.
Organic synthesis has historically relied on solution-phase, polar transformations to forge new bonds. However, this paradigm is evolving, propelled by the rapid evolution of radical chemistry. Additionally, organic synthesis is witnessing a simultaneous resurgence in mechanochemistry, the formation of new bonds in the solid-state, further contributing to this shift in the status quo. The aforementioned advances in radical chemistry have predominantly occurred in the solution phase, while the majority of mechanochemical synthesis advances feature polar transformations. Herein, we discuss a rapidly advancing area of organic synthesis: mechanochemical radical reactions. Solid-state radical reactions offer improved green chemistry metrics, better reaction outcomes, and access to intermediates and products that are difficult or impossible to reach in solution. This review explores these reactions in the context of small molecule synthesis, from early findings to the current state-of-the-art, underscoring the pivotal role solid-state radical reactions are likely to play in advancing sustainable chemical synthesis.
从历史上看,有机合成一直依赖于溶液相中的极性转化来形成新的化学键。然而,在自由基化学迅速发展的推动下,这种模式正在演变。此外,有机合成领域正在经历机械化学的复兴,即在固态中形成新的化学键,这进一步促成了这种现状的转变。自由基化学的上述进展主要发生在溶液相中,而大多数机械化学合成进展的特点是极性转化。在此,我们讨论有机合成中一个快速发展的领域:机械化学自由基反应。固态自由基反应具有更好的绿色化学指标、更优的反应结果,并且能够获得在溶液中难以或无法得到的中间体和产物。本综述从小分子合成的角度探讨了这些反应,从早期发现到当前的技术水平,强调了固态自由基反应在推动可持续化学合成中可能发挥的关键作用。