化学
环丁酮
烯丙基重排
肟
区域选择性
环戊酮
戒指(化学)
催化作用
键裂
药物化学
劈理(地质)
立体化学
有机化学
断裂(地质)
工程类
岩土工程
作者
Jing‐Feng Zhao,Pin Gao,Xin‐Hua Duan,Li‐Na Guo
标识
DOI:10.1002/adsc.201701630
摘要
Abstract An iron‐catalyzed radical allylation of cyclobutanone oxime esters with allylic sulfones via C−C bond cleavage is reported. This protocol provides a straight‐forward approach to cyanoalkylated alkenes with good functional group tolerance and high regioselectivity. Furthermore, this reaction can be further expanded to ring‐opening of less‐strained cyclopentanone oxime esters, leading to desired cyanoalkylated alkenes in good yields. magnified image
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