One-pot and regioselective synthesis of 3,4-dihydroquinazolines by Sequential Ugi/Staudinger/aza-Wittig reaction starting from functionalized isocyanides
2017
Xiong, Jun | Wei, Xiao | Yan, Yan-Mei | Ding, Ming-Wu
A new one-pot and regioselective synthesis of 3,4-dihydroquinazolines by Ugi/Staudinger/aza-Wittig sequence has been developed. The Ugi-type reaction of 2-azidobenzylisocyanide, aldehyde, secondary amine and acid produced an azide intermediate, which was then treated with triphenylphosphine to give 3,4-dihydroquinazolines regioselectively in good overall yields by Staudinger/aza-Wittig reaction at room temperature.
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书目信息
出版者
Elsevier Science
其它主题
Ovgmcjybvlltpb-uhfffaoysa-n; Secondary amine; Ngcpcpzrgbiuhg-uhfffaoysa-n; Aza-wittig reaction; Mjcozhrhtasxch-uhfffaoysa-n; Ambient temperature; Ugi reaction; Rwiftaxsnvpttg-uhfffaoysa-n; 4-dihydroquinazoline; Isocyanide; Qwjwizjlbifojj-uhfffaoysa-n
语言
英语
注释
Pre-press version
类型
Journal Article; Text
2024-02-27
MODS