Malekafzali A, Malinovska K, Patureau F W
FB Chemie , Technische Universiät Kaiserslautern , Erwin-Schrödinger Str. 52 , 67663 Kaiserslautern , Germany . Email:
Chemistry Department , Tarbiat Modares University , Jalale-Ale-Ahmad Highway , 14117-13116 Tehran , Iran.
New J Chem. 2017 Aug 7;41(15):6981-6985. doi: 10.1039/c7nj01666b. Epub 2017 Jun 30.
Due to the relative stability of the cumyl radical, cumenes and α-methyl-styrenes are ideally structured to directly harvest the oxidizing reactivity of O and initiate radical chain reactions in catalyst-free conditions. In the absence of additional substrates, these processes can lead to acetophenones. In the presence of substrates, the cumene oxidation process can be intercepted in various chain reactions, affording very simple protocols for functional group oxidation.
由于枯基自由基的相对稳定性,异丙苯和α-甲基苯乙烯具有理想的结构,能够在无催化剂条件下直接利用氧的氧化反应活性并引发自由基链反应。在没有其他底物的情况下,这些过程会生成苯乙酮。在有底物存在时,异丙苯氧化过程可在各种链反应中被截获,从而提供了非常简单的官能团氧化方案。