弗里德尔-克拉夫茨反应
镧系元素
三氟甲磺酸
酰化
催化作用
化学
有机化学
离子
作者
Atsushi Kawada,Shuichi Mitamura,Sh Kobayashi
出处
期刊:Journal of the Chemical Society
[The Royal Society of Chemistry]
日期:1993-01-01
卷期号: (14): 1157-1157
被引量:122
摘要
The Friedel-Crafts acylation of substituted benzenes proceeds smoothly by using a catalytic amount of a lanthanide trifluoromethanesulfonate [Ln(OTf)3], which is easily recovered from the reaction mixture and reused without a decrease in catalytic activity.
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