摘要
β-Substituted enones have been considered less reactive in Baylis-Hillman reaction. The reaction of cyclicenones is sluggish or does not occur at all under traditional conditions. [1] Therefore, substituted cyclic enones havebeen less explored in Baylis-Hillman reaction due to the extremely low reactivity. In this communication, we reported Baylis-Hillman reaction of substituted cyclic enones using our previously developed conditions with imidazole as catalyst. The reaction proceeded smoothly in aqueous media affording the desired product with good yields and moderate diastereoselectivity.……
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2003年第z1期168-168,共1页
Chinese Journal of Organic Chemistry
基金
Project supported by the National Natural Science Foundation of China (NSFC), the Ministry of Science and Technology (MoST), and the Institute of Chemistry (CAS).