化学
烷基化
芳基
基础(拓扑)
组合化学
催化作用
铃木反应
立体化学
有机化学
烷基
数学
数学分析
作者
Weiqin Jiang,James J. Fiordeliso,Zhihua Sui
标识
DOI:10.1080/00397910701215957
摘要
Abstract A series of novel 3,3‐dialkylated imidazopyridinones bearing 6‐aryl groups were designed as mimetics of active progesterone antagonists, 3,3‐disubstituted‐5‐arylindoles. The four‐step synthetic route is described. The key steps are base‐catalyzed cyclization, base‐catalyzed alkylation, and Suzuki coupling reaction.
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