摘要
报道了一种铜催化的1-芳基-1-环醇和1,3-二羰基化合物的环化反应,以中等到优秀的产率合成了一系列环烷烃稠合的二氢呋喃衍生物.该反应条件温和,官能团兼容性好.机理研究表明此环合反应可能经历了自由基中间体.
A novel method of copper-catalyzed cyclization of 1-aryl-1-cycloalcohols and 1,3-dicarbonyl compounds has been developed,affording various cycloalkane-fused dihydrofurans in moderate to excellent yields.This transformation proceeds under mild conditions and with a good tolerance of functional groups.The mechanistic investigation revealed that the reaction involved radical intermediates.
作者
杨胜彪
李燕
张前
Yang Shengbiao;Li Yan;Zhang Qian(Department of Chemistry,Northeast Normal University,Changchun 130024;State Key Laboratory of Organometallic Chemistry,Shang Hai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032)
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2019年第8期2226-2234,共9页
Chinese Journal of Organic Chemistry
基金
Project supported by the National Natural Science Foundation of China(No.21831002)
Ten Thousand Talents Program~~