离子液体
催化作用
选择性
化学
金属
反应条件
反应机理
组合化学
转化(遗传学)
离子键合
离子
有机化学
生物化学
基因
作者
Jiayin Hu,Jun Ma,Qinggong Zhu,Zhaofu Zhang,Congyi Wu,Buxing Han
标识
DOI:10.1002/anie.201411969
摘要
Protic ionic liquids (PILs), such as 1,8-diazabicyclo[5.4.0]-7-undecenium 2-methylimidazolide [DBUH][MIm], can catalyze the reaction of atmospheric CO2 with a broad range of propargylic amines to form the corresponding 2-oxazolidinones. The products are formed in high yields under mild, metal-free conditions. The cheaper and greener PILs can be easily recycled and reused at least five times without a decrease in the catalytic activity and selectivity. A reaction mechanism was proposed on the basis of a detailed DFT study which indicates that both the cation and anion of the PIL play key synergistic roles in accelerating the reaction.
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