摘要
氮杂环卡宾(NHC)催化下α-溴代烯醛和烯胺酮的[3+3]环化反应的区域选择性受温度控制.在35℃时,该反应能够区域专一性地给出稠合吡喃酮衍生物,而不是文献报道的喹啉酮类化合物.该方法反应条件温和、底物范围广、产率高、操作简便,为吡喃酮骨架的高效构建提供了新思路.
The regioselectivity of N-heterocyclic carbene(NHC)-catalyzed[3+3]annulation ofα-bromoenal with enaminone is dependent on the temperature.The reactions performed at 35℃could regiospecifically give the derivatives of fused pyranone instead of previously reported quinolones,which provided a new shortcut to pyranone with mild reaction condition,broad substrate scope,high yields and operational simplicity.
作者
王占林
李如一
钱辉旻
姚昌盛
Wang Zhanlin;Li Ruyi;Qian Huimin;Yao Changsheng(Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials,School of Chemistry and Materials Science,Jiangsu Normal University,Xuzhou 221116)
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2019年第7期2075-2083,共9页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(Nos.21871113,21372101)资助项目~~