期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 -, 期 -, 页码 -出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.3c01123
关键词
-
The Doebner hydrogen-transfer reaction has been developed for synthesizing substituted quinolines from anilines with electron-withdrawing groups. This reaction overcomes the low yield problem encountered in the conventional Doebner reaction. It can be applied to anilines with both electron-withdrawing and electron-donating groups, making it suitable for large-scale synthesis of bioactive molecules.
The Doebner hydrogen-transfer reaction has been developed for the synthesis of substituted quinolines from anilines possessing electron-withdrawing groups, which are known to give products in low yields when used in the conventional Doebner reaction. This reaction can be applied to not only anilines having electron-withdrawing groups but also those having electron-donating groups and can be used in the large-scale synthesis of bioactive molecules.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据