氧化磷酸化
三嗪
化学
甲烷氧化偶联
光化学
联轴节(管道)
药物化学
有机化学
材料科学
生物化学
甲烷
冶金
作者
Xuewu Fu,Ranran Feng,Yushi Tan,Hong‐Yu Zhang,Yuecheng Zhang,Jiquan Zhao
标识
DOI:10.1021/acs.joc.5c01352
摘要
An unprecedented C6-H hydroxyalkylation of 1,2,4-triazine-3,5(2H,4H)-dione was achieved using readily available and inexpensive alcohols as the coupling partner, low-toxicity 2-tert-butylanthraquinone as the photocatalyst, sodium bicarbonate as the base, and air as the green oxidant via oxidative cross-dehydrogenative-coupling. The reaction conditions are mildly carried out under visible-light induction with good functional group tolerance and a wide substrate scope. A series of mechanistic exploration experiments demonstrated that the reaction proceeds via a radical mechanism. In addition, gram-scale experiments and application studies indicated that this method has a bright practical prospect.
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