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Iron‐Catalyzed Ring‐Opening/Allylation of Cyclobutanone Oxime Esters with Allylic Sulfones
Advanced Synthesis & Catalysis ( IF 5.4 ) Pub Date : 2018-03-14 , DOI: 10.1002/adsc.201701630
Jing-Feng Zhao 1 , Pin Gao 1 , Xin-Hua Duan 1 , Li-Na Guo 1
Affiliation  

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.

中文翻译:

铁催化的环丁酮肟酯与烯丙基砜的开环/烯丙基化

据报道,通过CC键裂解,铁催化的环丁酮肟酯与烯丙基砜的自由基烯丙基化反应。该协议为氰基烷基化烯烃提供了一种简单易行的方法,具有良好的官能团耐受性和较高的区域选择性。此外,该反应可以进一步扩展到较少应变的环戊酮肟酯的开环反应,从而以高收率得到所需的氰基烷基化烯烃。
更新日期:2018-03-14
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