Cong Fei, Wei Yongliang, Tang Pingping
State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.
Chem Commun (Camb). 2018 Apr 26;54(35):4473-4476. doi: 10.1039/c8cc01096j.
The first example of an azidotrifluoromethoxylation of styrenes has been achieved by synergistic visible-light-mediated photoredox and silver catalysis. Trifluoromethyl arylsulfonate (TFMS) and the Zhdankin reagent were used as the trifluoromethoxylation reagent and the azide source, respectively. A good functional group tolerance and mild reaction conditions of this method are applicable to late-stage azidotrifluoromethoxylation of complex small molecules. Furthermore, the mechanistic investigations indicate the single-electron transfer involved in the reaction.
通过协同可见光介导的光氧化还原和银催化,实现了苯乙烯叠氮化三氟甲氧基化的首例反应。分别使用三氟甲基芳基磺酸酯(TFMS)和日丹金试剂作为三氟甲氧基化试剂和叠氮源。该方法具有良好的官能团耐受性和温和的反应条件,适用于复杂小分子的后期叠氮化三氟甲氧基化反应。此外,机理研究表明该反应涉及单电子转移。