Asymmetric epoxidation of α,β-unsaturated ketones via an amine-thiourea dual activation catalysis
2021
Zhang, Lu-Wen | Wang, Li | Ji, Nan | Dai, Si-Yang | He, Wei
A simple asymmetric epoxidation method is developed to effectively synthesize chiral α-carbonyl epoxides through an amine-thiourea dual activation catalysis. In this method, TBHP, as an oxidant, determined the reaction rate, and the chiral amine-thiourea catalyst effectively controlled the stereoselectivity of the reaction, and KOH promoted deprotonation. 22 examples of α,β-unsaturated ketones with various substituent groups are smoothly converted into α-carbonyl epoxides with moderate to excellent enantiomeric excess.
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书目信息
出版者
Botanical Society of America
其它主题
Chiral amine-thiourea; Organocatalyst; Asymmetric epoxidation; Stereoselectivity; Deprotonation; Epoxidation reactions
语言
英语
类型
Journal Article; Text
2024-02-28
MODS