摘要
发展了一种镍催化环丁酮肟酯和芳基锌试剂之间Negishi偶联的方法.镍既作为亚胺自由基的引发剂,也作为芳基锌试剂与烷基自由基偶联反应的催化剂在反应中起作用.本方法可避免使用剧毒的氰化物,且具有很广的底物适应性和官能团兼容性,因此可能是一种具有潜在吸引力的高效合成烷基腈类化合物的新策略.初步的机理研究显示,该反应极可能经历自由基历程.
A nickel-catalyzed Negishi coupling of cyclobutanone oxime esters with aryl zinc reagents has been developed,in which nickel serves both as an initiator for imine radicals and a catalyst for the coupling of aryl zinc reagents with oxime esters.The protocol can avoid the use of poisonous cyanide and has broad substrate scope as well as good functional group compatibility.Therefore,this method provides an attractive strategy for the synthesis of valuable nitriles.Preliminary mechanistic studies indicate that a radical pathway is involved in the product formation.
作者
帅斌
李兆明
裘晖
方萍
梅天胜
Shuai Bin;Li Zhao-Ming;Qiu Hui;Fang Ping;Mei Tian-Sheng(State Key Laboratory of Organometallic Chemistry Center for Excellence in Molecular Synthesis Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences Chinese Academy of Sciences,Shanghai 200032)
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2020年第3期651-662,共12页
Chinese Journal of Organic Chemistry
基金
中国科学院战略性先导科技专项(No.XDB20000000)
国家自然科学基金(Nos.21572245,21772222,21772220)
上海市科委(Nos.17JC1401200,18JC1415600)资助项目.