In 2019,Organic Letters included an article by Huang, Chen; Feng, Jie; Ma, Rui; Fang, Shuaishuai; Lu, Tao; Tang, Weifang; Du, Ding; Gao, Jian. Recommanded Product: 24388-23-6. The article was titled ãRedox-Neutral Borylation of Aryl Sulfonium Salts via C-S Activation Enabled by Lightã? The information in the text is summarized as follows:
Reported here is a novel photoinduced strategy for the borylation of aryl sulfonium salts using bis(pinacolato)diboron as the B source. This method exploits redox-neutral aryl sulfoniums to gain access to aryl radicals via C-S bond activation upon photoexcitation under transition-metal-free conditions. Therefore, it grants access to diverse arylboronate esters with good performance from easily available aryl sulfoniums accompanied by mild conditions, operational simplicity, and easy scalability. After reading the article, we found that the author used 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane(cas: 24388-23-6Recommanded Product: 24388-23-6)
4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane(cas: 24388-23-6) can be used as a substrate in the study of Suzuki–Miyaura coupling of various aryl iodides over SiliaCat Pd(0).Recommanded Product: 24388-23-6
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