呋喃
催化作用
亚甲基
基质(水族馆)
化学
吡咯
功能群
甲烷氧化偶联
有机化学
药物化学
反应条件
酮
组合化学
海洋学
地质学
聚合物
作者
Lingkai Kong,Xueping Hu,Li‐Ping Bai
出处
期刊:ACS omega
[American Chemical Society]
日期:2022-01-07
卷期号:7 (2): 2337-2343
被引量:8
标识
DOI:10.1021/acsomega.1c06216
摘要
An efficient and green route of C-C bond formation was disclosed to construct 2,3-diaryl-1,4-diketones from α-methylene ketones by the catalysis of tetrabutylammonium iodide (TBAI) with tert-butyl hydroperoxide (TBHP) as an oxidant in water. This reaction affords the desired products in good to excellent yields from readily available materials, with a broad substrate scope, good functional group tolerance, and mild reaction conditions. Furthermore, tetrasubstituted furan and pyrrole were smoothly constructed from α-methylene ketones in one pot with 96 and 90% yields, respectively.
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