氰化
化学
钯
芳基
催化作用
卤素
化学计量学
组合化学
有机化学
烷基
作者
Keiichiro Iizumi,Hiroki Tanaka,Kei Muto,Junichiro Yamaguchi
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-04-29
卷期号:26 (18): 3977-3981
被引量:4
标识
DOI:10.1021/acs.orglett.4c01118
摘要
A denitrative cyanation of nitroarenes using organocyanides and a palladium catalyst was developed. The key for this reaction was the utilization of an aminoacetonitrile as a cyano source to avoid the generation of stoichiometric metal- and halogen-containing chemical waste. A wide range of nitroarenes, including heteroarenes and pharmaceutical molecules, can be converted into aryl nitriles.
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